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Project Manager, Marketing Operations Material Review
AbbVie Inc. - Mettawa, IL, United StatesIndexed from Smartrecruiters Benefit evidence checked May 7, 20266 days agoWhy we showed this
Unspecified Marketing - Senior Resolvable source Verified parental leave: 12 wksource Resolvable source Verified non-birth-parent leave: 12 wksource Salary not disclosed Inferred from posting 401(k) reportedProject Manager, Marketing Operations Material Review Mettawa, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Project Manager, Marketing Operations Material Review facilitates the management of Advertising & Promotional materials as they pertain to the U.S. Commercial MRP (Material Review Process). The Project Manager, Marketing Operations Material Review ensures: Facilitation of cross-functional team (Medical, Regulatory, Commercial, Legal, Compliance, others) review and approval of: Advertising materials Promotional materials Sales Training materials Promotional Labeling materials Management of cross functional team members and advertising agencies Open communication of material status with cross-functional team members and advertising agencies Tactical support and project timeline oversight of materials through MRP Consulting and training support to all team members responsible for uploading and approving materials within the MRP Timely review of all promotional, non-promotional materials through U.S. Commercial, Medical reviewers, Regulatory reviewers, and other key stakeholders Additionally, provides key support for: Solutions and contingency plans to facilitate business success Holds self and team accountable for results Serves as a mentor and coaches others on the MRP Proactively provides consulting; expertise
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Varicent Solution Architect
Intuitive Surgical, Inc. - Sunnyvale, CA, United StatesIndexed from Smartrecruiters Benefit evidence checked May 7, 20266 days agoWhy we showed this
Unspecified Engineering - Mid Resolvable source Verified parental leave: 8 wksource Resolvable source Verified non-birth-parent leave: 8 wksource Salary not disclosedVaricent Solution Architect Sunnyvale, CA, United States Company Description: It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at Intuitive . As a global leader in robotic-assisted surgery and minimally invasive care , our technologies-like the da Vinci surgical system and Ion -have transformed how care is delivered for millions of patients worldwide. We're a team of engineers, clinicians, and innovators united by one purpose: to make surgery smarter, safer, and more human. Every day, our work helps care teams perform with greater precision and patients recover faster, improving outcomes around the world. The problems we solve demand creativity, rigor, and collaboration. The work is challenging, but deeply meaningful-because every improvement we make has the potential to change a life. If you're ready to contribute to something bigger than yourself and help transform the future of healthcare , you'll find your purpose here. Job Description: Primary Function of this Position: Position Summary The Solution Architect - Varicent ICM serves as the technical and functional authority for the enterprise Varicent platform across the organization. In this highly visible role, you will be responsible for the end-to-end design, architecture, and delivery of complex incentive compensation solutions using both Varicent Designer and Varicent Studio. You will bring an AI first mindset with experience in using LLM models and machine learning to create organizational value. You will partner with senior stakeholders across Sales, Finance, and
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Medical Director, Hematology Clinical Development
AbbVie Inc. - North Chicago, IL, United StatesIndexed from Smartrecruiters Benefit evidence checked May 7, 20266 days agoWhy we showed this
Unspecified Engineering - Staff Plus Resolvable source Verified parental leave: 12 wksource Resolvable source Verified non-birth-parent leave: 12 wksource Salary not disclosed Inferred from posting 401(k) reportedMedical Director, Hematology Clinical Development North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Purpose: Oversees the direction, planning, execution and interpretation of clinical trials or research activities of a clinical development program. Participates in cross-functional teams to generate, deliver and interpret high-quality clinical data supporting overall product scientific and business strategy. Responsibilities: Manages the design and implementation of one or more clinical development programs in support of an overall Development Plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations and emerging issues. Oversees project-related education of investigators, study site personnel and AbbVie study staff. Responsibility may extend from early translational development activities to mature product lifecycle management strategies for internal and/or partnered programs. Has overall responsibility for oversight of clinical studies, monitoring overall study integrity and review, interpretation and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is responsible for oversight of study enrollment and overall timelines for key deliverables. Responsible for assessment
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Nurse (Temporal)
Intuitive Surgical, Inc. - Mexicali, MEXICO, MexicoIndexed from Smartrecruiters Benefit evidence checked May 7, 20266 days agoWhy we showed this
Unspecified Healthcare - Mid Resolvable source Verified parental leave: 8 wksource Resolvable source Verified non-birth-parent leave: 8 wksource Salary not disclosedNurse (Temporal) Mexicali, MEXICO, Mexico Company Description: It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at Intuitive . As a global leader in robotic-assisted surgery and minimally invasive care , our technologies-like the da Vinci surgical system and Ion -have transformed how care is delivered for millions of patients worldwide. We're a team of engineers, clinicians, and innovators united by one purpose: to make surgery smarter, safer, and more human. Every day, our work helps care teams perform with greater precision and patients recover faster, improving outcomes around the world. The problems we solve demand creativity, rigor, and collaboration. The work is challenging, but deeply meaningful-because every improvement we make has the potential to change a life. If you're ready to contribute to something bigger than yourself and help transform the future of healthcare , you'll find your purpose here. Job Description: Primary Function of Position: Assist company's Doctor with specialized medical attention for users and keeps record for all employees' medical references. Roles & Responsibilities: Responsible for medicine and first aid kits inventory Purchases medicines and medical equipment based in company needs. Keep all First Aid Kits stocks in good conditions and updated . Reports monthly medical attendance stats Provide medical care (i.e. taking blood pressure, etc.) and given first aid to the personnel went needed and based on internal medical protocol. Perform periodic medical tests to employees based
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da Vinci Clinical Territory Associate (m/w/d)
Intuitive Surgical, Inc. - Remote | Eisenach, TH, GermanyIndexed from Smartrecruiters Benefit evidence checked May 7, 20266 days agoWhy we showed this
Remote Healthcare - Mid Resolvable source Verified parental leave: 8 wksource Resolvable source Verified non-birth-parent leave: 8 wksource Salary not disclosedda Vinci Clinical Territory Associate (m/w/d) Remote | Eisenach, TH, Germany Company Description: It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at Intuitive . As a global leader in robotic-assisted surgery and minimally invasive care , our technologies-like the da Vinci surgical system and Ion -have transformed how care is delivered for millions of patients worldwide. We're a team of engineers, clinicians, and innovators united by one purpose: to make surgery smarter, safer, and more human. Every day, our work helps care teams perform with greater precision and patients recover faster, improving outcomes around the world. The problems we solve demand creativity, rigor, and collaboration. The work is challenging, but deeply meaningful-because every improvement we make has the potential to change a life. If you're ready to contribute to something bigger than yourself and help transform the future of healthcare , you'll find your purpose here. Job Description: The Clinical Territory Associate (CTA) will work closely with the Clinical Sales Manager to gain knowledge in all aspects of our business to include technical, clinical, and sales. He or She will train to be a da Vinci® Surgery technical and sales expert across all primary surgical specialties to develop surgical robotics programs in the assigned territory. During the first year of the job, the CTA will focus on the technical and clinical aspect of the job, and during the second year
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Accounts Receivable Specialist (Maternity Cover - fixed term)
Intuitive Surgical, Inc. - Madrid, SPAIN, SpainIndexed from Smartrecruiters Benefit evidence checked May 7, 20266 days agoWhy we showed this
Unspecified Finance - Mid Resolvable source Verified parental leave: 8 wksource Resolvable source Verified non-birth-parent leave: 8 wksource Salary not disclosedAccounts Receivable Specialist (Maternity Cover - fixed term) Madrid, SPAIN, Spain Company Description: At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints. As pioneer and leading company in the field of robotic-assisted surgery, we strive to foster an inclusive and diverse team, committed to making a difference. For more than 25 years, we have worked with hospitals and care teams around the world to help solve some of healthcare's hardest challenges and advance what is possible. Intuitive has been built by the efforts of great people from diverse backgrounds. We believe great ideas can come from anywhere-we strive to foster an inclusive culture built around diversity of thought and mutual respect. We lead with inclusion and empower our team members to do their best work as their most authentic selves. Join a team committed to taking big leaps forward for a global community of healthcare professionals and their patients. Together, let's advance the world of minimally invasive care. The Sr. Accounts Receivable Specialist supports the accounting function by ensuring accurate and timely processing of receivables, cash applications, and related accounting activities for Spain and Portugal. Working closely with Senior Accountants, FP&A, and external stakeholders, this role contributes to the execution of core AR and general accounting processes, supporting monthly close activities and ensuring compliance with company policies and internal controls. This is a temporary position providing coverage
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Scientist I, Analytical Development
AbbVie Inc. - Worcester, MA, United StatesIndexed from Smartrecruiters Benefit evidence checked May 7, 20266 days agoWhy we showed this
Unspecified Data - Mid Resolvable source Verified parental leave: 12 wksource Resolvable source Verified non-birth-parent leave: 12 wksource Salary not disclosed Inferred from posting 401(k) reportedScientist I, Analytical Development Worcester, MA, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Investigate, identify, develop, and optimize new methods and techniques to generate reliable and reproducible data in a timely manner. Read and adapt scientific literature to accomplish assignments and demonstrate broad and versatile technical expertise within discipline. Responsibilities Independently design, develop, and optimize robust analytical methods using separations-base techniques (HPLC, icIEF, CE-SDS) to characterize biopharmaceutical products Implement and innovate new experimental protocols/techniques. Understand the goal and maintain a high proficiency in his/her projects as well as the overall program. Interpret results and draw conclusions from own multistage experiments, note significant deviations, then suggest, design, and pursue relevant experiments. Understand relevant scientific literature and apply theoretical framework to solving problems within scientific discipline in a timely manner. Perform routine and complex tasks competently and independently and generate reliable and consistent results. Troubleshoot complex analytical issues and implement innovative solutions to improve method performance and efficiency. Impact projects mostly through lab and/or pilot plant based activities. Responsible for compliance with all applicable Corporate
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Director, HEOR Strategy, Neuroscience
AbbVie Inc. - Florham Park, NJ, United StatesIndexed from Smartrecruiters Benefit evidence checked May 7, 20266 days agoWhy we showed this
Unspecified Product - Staff Plus Resolvable source Verified parental leave: 12 wksource Resolvable source Verified non-birth-parent leave: 12 wksource Salary not disclosed Inferred from posting 401(k) reportedDirector, HEOR Strategy, Neuroscience Florham Park, NJ, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Leads the development & execution of projects for multiple on-market and/or pipeline development assets potentially across multiple geographies. Is the brand/asset leader representing HEOR on cross functional teams and in the pipeline commercialization teams. Accountable for HEOR strategies and execution, looks to shape brand/asset/enterprise strategies by bringing in expertise and experience within and beyond his/her subject matter expertise. Ensures project plans across all products within their TA portfolio integrates and aligns with the product strategy plans from matrix groups as well as commercial interests and scientific integrity of studies. W/a view across TA assets, ensures there is no overlap of projects and leverages endeavors across the TA; provides updates on execution of plans to products as well as functional management. In the development of product strategic plans, liaises with other members of the product team to generate innovative ideas and get buy-in to strategies Responsibilities List up to 10 main responsibilities for the job. Include information about the accountability
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Scientist I, Cell and Molecular Biologist
AbbVie Inc. - North Chicago, IL, United StatesIndexed from Smartrecruiters Benefit evidence checked May 7, 20266 days agoWhy we showed this
Unspecified Data - Mid Resolvable source Verified parental leave: 12 wksource Resolvable source Verified non-birth-parent leave: 12 wksource Salary not disclosed Inferred from posting 401(k) reportedScientist I, Cell and Molecular Biologist North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Description: AbbVie Oncology Discovery is seeking a highly motivated and experienced cancer cell biologist to support drug discovery projects in our in vitro cancer biology team with a focus on antibody-drug conjugates. The candidate will work closely with a team of experienced scientists to develop and optimize key pharmacological, biochemical and cell-based assays to support multiple programs. Key Responsibilities: Design and execute in vitro studies to assess novel antibody-drug conjugates Analyze and interpret experiments and present data to the broader project team and group meetings. Propose relevant follow-up experiments as needed. Troubleshoot and/or optimize experimental procedures as needed to further the program goals. Contribute to the preparation of data packages for scientific publications, regulatory documents, and patent applications Work independently in a fast paced, multi-tasking environment as part of a diverse research team. Collaborate with cross-functional teams to advance programs from early discovery to preclinical development Qualifications: Qualifications Required: Bachelor's Degree with 5 years of experience, or
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Director, Country Clinical Operations Management
AbbVie Inc. - Bengaluru, KA, IndiaIndexed from Smartrecruiters Benefit evidence checked May 7, 20266 days agoWhy we showed this
Unspecified Finance - Staff Plus Resolvable source Verified parental leave: 12 wksource Resolvable source Verified non-birth-parent leave: 12 wksource Salary not disclosed Inferred from posting 401(k) reportedDirector, Country Clinical Operations Management Bengaluru, KA, India Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Country Clinical Operations Manager is the key leader for Clinical Operations at the country level for both internal & external partners. Accountable for the strategic and operational management for clinical operations and clinical site management activities for the assigned country/ies. Responsible for leading the implementation of the corporate vision and objectives, operating across all therapeutics areas to support the execution of AbbVie's pipeline. The role is accountable for country clinical trial performance, providing strategic planning, oversight and direction of the country team to ensure on time, within budget and quality delivery of internally conducted clinical studies. The Country COM is accountable to develop a highly collaborative framework with internal and external key stakeholders across the local and global organization to best position AbbVie in advancing clinical research and accelerating the transformation of science into best-in-class medicines. •Defines the country strategy and operational plans aligned with AbbVie's business priorities, Clinical Development Operations and affiliate objectives in order to position the
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Senior Specialist or Manager,Medical Strategic Operations(Medical Information)
AbbVie Inc. - Minato City, Tokyo, JapanIndexed from Smartrecruiters Benefit evidence checked May 7, 20266 days agoWhy we showed this
Unspecified Sales - Senior Resolvable source Verified parental leave: 12 wksource Resolvable source Verified non-birth-parent leave: 12 wksource Salary not disclosed Inferred from posting 401(k) reportedSenior Specialist or Manager,Medical Strategic Operations(Medical Information) Minato City, Tokyo, Japan 企業概要: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. 求人内容: Senior Specialist サマリー: このポジションは、実務担当者として、インタビューフォームやくすりのしおり等の資材作成の他、薬剤のプロモーション前に病院薬剤部が実施するヒアリングに必要な資料の整備など、日本のregulation上必要なメディカルインフォメーション(MI)業務を行い、新薬の上市と発売後の薬剤の適正使用をサポートします。また、Global Medical Information (GMI)の目標達成のために、Large Business Unit (LBU)に戦略的・運用的サポートの提供や、GMIとAlignしながら、Regional MIチームと連携し、Affiliateにおける業務を行います。Best Practiceへの助言やAffiliateにおける分析レポートのステークホルダーへの共有、MIプロセスに関するトレーニング、ファーマコビジランス、製品監視、その他の関連関係者との連絡役も担います。また、メディカルにおけるデジタル化推進やその他のメディカルオペレーション業務なども担当します。 主な職責: 日本 の regulation で求められる MI の役割: 「インタビューフォーム」や「くすりのしおり」など、規制上必須となる資料の作成を主導し、それぞれ医薬品医療機器総合機構(PMDA)および薬剤リスク・ベネフィット評価分析・対応(RAD-AR)機構へ情報・資料を提出する 添付文書の改訂や新たな適応追加に応じて、これらの資料を適宜更新する コマーシャル部門による販促活動前に必須となる、病院薬剤部による薬剤ヒアリングに必要な資料を整備し、営業部門による製品上市活動を支援する。 国内事項の MI 専門家としての役割: データプライバシー、ファーマコビジランス、規制諸業務等についてのローカルビジネスに精通し、データプライバシーに関するregulationの情報をRegional MIデータベースへ提供する 日本国内のregulationや組織ポリシー遵守のための指導やサポートを行う MI機能・プロセス強化のためのデジタルソリューション導入やその統括を行う 問い合わせデータを分析し、insight抽出を行い、分析レポートを作成する Regionおよび国内ステークホルダーへinsightや、問い合わせ傾向、重要トピックを共有する Insightや重要な問い合わせに関する日本国内のフィードバックをGMIへ共有する トレーニングやフォーラムの実施: 必要に応じて国内チーム向けに、MIトレーニングを企画し実施する。 Regional MIチームと連携し、プロセス・規制・GMI目標の変化に合わせてトレーニング教材を定期更新する MIフォーラムや、国内メディカルアフェアーズ、国内メディカルオペレーションの会議などに積極的に参加し、インサイトやベストプラクティス、重要情報を共有する その他メディカルオペレーション業務: メディカルアフェアーズ/オペレーションリーダーの要請に応じ、その他ローカルの業務へ対応する 業務に必要な費用の把握と予算に応じたプロジェクトの実行 Manager サマリー: このポジションは、実務担当者として、インタビューフォームやくすりのしおり等の資材作成の他、薬剤のプロモーション前に病院薬剤部が実施するヒアリングに必要な資料の整備など、日本のregulation上必要なメディカルインフォメーション(MI)業務を行い、新薬の上市と発売後の薬剤の適正使用をサポートします。また、Global Medical Information (GMI)の目標達成のために、Large Business Unit (LBU)に戦略的・運用的サポートの提供や、GMIとAlignしながら、Regional MIチームと連携し、Affiliateにおける業務を行います。Best Practiceへの助言やAffiliateにおける分析レポートのステークホルダーへの共有、MIプロセスに関するトレーニング、ファーマコビジランス、製品監視、その他の関連関係者との連絡役も担います。また、メディカルにおけるデジタル化推進やその他のメディカルオペレーション業務なども担当します。 主な職責: 日本 の regulation で求められる MI の役割: 「インタビューフォーム」や「くすりのしおり」など、規制上必須となる資料の作成を主導し、それぞれ医薬品医療機器総合機構(PMDA)および薬剤リスク・ベネフィット評価分析・対応(RAD-AR)機構へ情報・資料を提出する 添付文書の改訂や新たな適応追加に応じて、これらの資料を適宜更新する コマーシャル部門による販促活動前に必須となる、病院薬剤部による薬剤ヒアリングに必要な資料を整備し、営業部門による製品上市活動を支援する。 国内事項の MI 専門家としての役割: データプライバシー、ファーマコビジランス、規制諸業務等についてのローカルビジネスに精通し、データプライバシーに関するregulationの情報をRegional MIデータベースへ提供する 日本国内のregulationや組織ポリシー遵守のための指導やサポートを行う MI機能・プロセス強化のためのデジタルソリューション導入やその統括を行う 問い合わせデータを分析し、insight抽出を行い、分析レポートを作成する Regionおよび国内ステークホルダーへinsightや、問い合わせ傾向、重要トピックを共有する Insightや重要な問い合わせに関する日本国内のフィードバックをGMIへ共有する トレーニングやフォーラムの実施: 必要に応じて国内チーム向けに、MIトレーニングを企画し実施する。 Regional MIチームと連携し、プロセス・規制・GMI目標の変化に合わせてトレーニング教材を定期更新する MIフォーラムや、国内メディカルアフェアーズ、国内メディカルオペレーションの会議などに積極的に参加し、インサイトやベストプラクティス、重要情報を共有する その他メディカルオペレーション業務: メディカルアフェアーズ/オペレーションリーダーの要請に応じ、その他ローカルの業務へ対応する 業務に必要な費用の把握と予算に応じたプロジェクトの実行 資格: Senior Specialist 必須スキル・経験 細部への注意力、優れた分析力、明確・簡潔な口頭および書面コミュニケーション能力 クリティカルシンキングで医療情報資料の調査・分析・評価、関連する指示・ポリシー・ガイドラインの解釈・適用 医薬品の原則と実務、その応用、医療用語や治療法、薬理学分野の知識・理論・応用能力 プロセス改善・高品質基準維持の推進力 関係部門や外部ベンダーとの調整・コミュニケーション能力 地域横断プロジェクトを主導した経験や多様なチーム間の調整力 文化・医療/臨床実践の差異への感受性 英語によるコミュニケーション能力 応募資格 理系または、医療系の学士を有していること、かつ、2年以上の製薬企業での勤務経験、または、医療分野4年以上の勤務経験を有していること。PhDであれば尚可 インターン・レジデンシー経験も可。 博士号(PharmD, PhD)に加えて、製薬等の実務経験3年以上あれば尚可。 最新の規制(欧州医薬品庁、PMDA、FDA等)やAbbVie治療領域・研究領域への知識があれば尚可 Manager 必須スキル・経験 細部への注意力、優れた分析力、明確・簡潔な口頭および書面コミュニケーション能力 クリティカルシンキングで医療情報資料の調査・分析・評価、関連する指示・ポリシー・ガイドラインの解釈・適用 医薬品の原則と実務、その応用、医療用語や治療法、薬理学分野の知識・理論・応用能力 プロセス改善・高品質基準維持の推進力 関係部門や外部ベンダーとの調整・コミュニケーション能力 地域横断プロジェクトを主導した経験や多様なチーム間の調整力 文化・医療/臨床実践の差異への感受性 英語によるコミュニケーション能力 チームマネジャーのサポートおよびチーム員のスキルアップ 応募資格 理系または、医療系の学士を有していること、かつ、2年以上の製薬企業での勤務経験、または、医療分野4年以上の勤務経験を有していること。PhDであれば尚可 インターン・レジデンシー経験も可。 博士号(PharmD, PhD)に加えて、製薬等の実務経験3年以上あれば尚可。 最新の規制(欧州医薬品庁、PMDA、FDA等)やAbbVie治療領域・研究領域への知識があれば尚可。 共通 マインド: 患者さん中心/Patient Centric One AbbVieとして/All for one AbbVie 賢明かつ確実な判断/Decide Smart and Sure 迅速性と責任感/Agile and Accountable 明確に、そして勇敢に/Clear and Courageous 可能性の実現/Make Possibilities Real インテグリティ/Integrity その他の情報: 経験値、面接結果により「Specialist(G14)」での合格となる場合があります。 アッヴィは、機会均等を重視する雇用主であり、誠実な企業活動、革新の推進、人々の生活への貢献、そして地域社会への貢献に努めています。雇用機会均等に向けて、障がいを持つ方々も積極的に支援しています。
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MSL
AbbVie Inc. - Remote | Jinan, Shandong, ChinaIndexed from Smartrecruiters Benefit evidence checked May 7, 20266 days agoWhy we showed this
Remote Other - Mid Resolvable source Verified parental leave: 12 wksource Resolvable source Verified non-birth-parent leave: 12 wksource Salary not disclosed Inferred from posting 401(k) reportedMSL Remote | Jinan, Shandong, China Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: • Maintain updated medical knowledge of assigned therapeutic are • Create and update medical training and communication material and deliver the training/communication efficiently • Participate proactively in PPD medical projects and events, including study operation, meeting organization, etc. as coordinator • Develop advocacy for company and product by sustained KOL and prescriber liaison • Provide medical advice on PPD product medical communication, under the guidance from medical advisors Qualifications: • Medical doctor background of the assigned therapeutic area with bachelor degree or above • Good communication and coordination skills or potentials • Fluent English in reading, writing and oral communication. • Working experience in medical dept. of multinational pharmaceutical company and related dept. in hospital is a plusCoach junior members within team • People management (if applicable)• Response to medical inquiry, under the guidance from medical advisors • Other necessary medical liaison activities Additional Information: AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives
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Senior Manager Regulatory Affairs US Advertising and Promotion - US Specialty
AbbVie Inc. - Florham Park, NJ, United StatesIndexed from Smartrecruiters Benefit evidence checked May 7, 20266 days agoWhy we showed this
Unspecified Other - Senior Resolvable source Verified parental leave: 12 wksource Resolvable source Verified non-birth-parent leave: 12 wksource Salary not disclosed Inferred from posting 401(k) reportedSenior Manager Regulatory Affairs US Advertising and Promotion - US Specialty Florham Park, NJ, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Senior Manager, Regulatory Affairs US Advertising and Promotion - US Specialty combines knowledge of scientific, regulatory and business issues to enable products that are developed, manufactured or distributed to meet the required legislation. Additionally, the individual develops and supervises regulatory professionals as needed. Supports the Director in efforts to influence the regulatory environment. The Senior Manager has department/group/site level influence and is generally recognized as an expert and resource and leads the department as a subject matter expert (SME) for Regulatory. This individual share knowledge and expertise with others in support of team activities and analyzes broad scope implications of changing regulations and policies. Responsibilities: Proactively captures and disseminates activities of government, industry, and trade associations that impact pharmaceutical regulatory policies relative to AbbVie's interests. Maintains awareness of pending changes to communicate impact and relevance within Regulatory Operations. Drafts and finalizes comments in a timely manner to regulators and trade associations.
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Associate Director, Clinical Pharmacology
AbbVie Inc. - Waltham, MA, United StatesIndexed from Smartrecruiters Benefit evidence checked May 7, 20266 days agoWhy we showed this
Unspecified Healthcare - Staff Plus Resolvable source Verified parental leave: 12 wksource Resolvable source Verified non-birth-parent leave: 12 wksource Salary not disclosed Inferred from posting 401(k) reportedAssociate Director, Clinical Pharmacology Waltham, MA, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Conceives, executes and effectively manages and communicates multi-disciplinary Clinical Pharmacology development plans and strategies that achieve commercial goals and regulatory requirements for multiple functions. Generates new PK/PD study proposals and leads those efforts. Anticipates and critically evaluates Clinical Pharmacology, PK/PD or regulatory advances, strengths, weaknesses, opportunities and threats, and responds with appropriate new strategies. Consistently demonstrates excellent record of accomplishment of Clinical Pharmacology and business objectives. Leads Clinical Pharmacology/PK/PD aspects of multiple projects. Responsible for critically evaluating technical and scientific aspects along with Clinical Pharmacology and Pharmacometrics management. Responsibilities Accountable for Phase 1-4 studies design, and clinical pharmacology strategy; acts as the representative for project(s). Executes strategy, lead teams and various data analyses and interpretation by providing necessary context (including explaining MoA and disease specifics, available relevant internal and external data, analysis plans, interpretation and discussion of model results in the context of research question). Author regulatory documents including protocols, study reports, population PK reports, exposure-response analyses reports, CTDs, label
- 6 days ago
Why we showed this
Unspecified Other - Mid Resolvable source Verified parental leave: 10 wksource Resolvable source Verified non-birth-parent leave: 10 wksource Salary not disclosed Inferred from posting 401(k) reportedUntitled role Location not specified posted:
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QA Operations Compliance Specialist
AbbVie Inc. - Sligo, SO, IrelandIndexed from Smartrecruiters Benefit evidence checked May 7, 20266 days agoWhy we showed this
Unspecified Finance - Mid Resolvable source Verified parental leave: 12 wksource Resolvable source Verified non-birth-parent leave: 12 wksource Salary not disclosed Inferred from posting 401(k) reportedQA Operations Compliance Specialist Sligo, SO, Ireland Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Innovate with intention. Science is at the heart of what we do. People are at the heart of why we do it. Welcome to AbbVie! We are a global, research-based biopharmaceutical company that combines the focus and passion of leading-edge biotech with the expertise and capability of an established pharmaceutical leader. Redefining what is possible is our business and our passion. Our goal is to help patients live healthier lives and we are proud to be a Great Place to Work. We are recruiting a QA Operations Compliance Specialist to join our site in Ballytivnan, Sligo. Are you intrigued? Do you want to learn more? A snapshot of your key responsibilities as a QA Operations Compliance Specialist would be: Ensuring that all products leaving AbbVie Biologics department meet the standards required for marketed and investigational drug products. Ensuring that products and aseptic process simulations manufactured at AbbVie Biologics meet the requirements of the end users, regulatory authorities and of the company.
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Account Specialist - Skincare & Contouring
AbbVie Inc. - Remote | Guangzhou, Guangdong Province, ChinaIndexed from Smartrecruiters Benefit evidence checked May 7, 20266 days agoWhy we showed this
Remote Sales - Mid Resolvable source Verified parental leave: 12 wksource Resolvable source Verified non-birth-parent leave: 12 wksource Salary not disclosed Inferred from posting 401(k) reportedAccount Specialist - Skincare & Contouring Remote | Guangzhou, Guangdong Province, China Company Description: About AbbVie At Allergan Aesthetics, an AbbVie company, we develop, manufacture, and market a portfolio of leading aesthetics brands and products. Our aesthetics portfolio includes facial injectables, body contouring, plastics, skin care, and more. Our goal is to consistently provide our customers with innovation, education, exceptional service, and a commitment to excellence, all with a personal touch. For more information, visit https://global.allerganaesthetics.com/. Follow Allergan Aesthetics on LinkedIn. Job Description: 艾尔建美学 公司介绍: 作为一家艾伯维旗下的公司,艾尔建美学致力于研发、生产和销售一系列先进的美学品牌和产品。旗下美学产品组合覆盖面部美学、身体塑形、整形、皮肤护理等领域。我们的目标是始终如一地为客户提供优质的创新产品、培训教育和专业服务,向他们传递信心。欲了解更多信息,请访问 https://global.allerganaesthetics.com/。在领英上关注艾尔建美学 。 客户专员- 皮肤美容与塑形 岗位职责: 推动业务目标:制定并执行所负责机构的酷塑与丝缇珂销售计划,通过积极的业务活动和策略达到业务目标,并不断努力提升业绩。 客户机会洞察:深入了解皮肤美容与塑形产品线,挖掘并掌握客户需求,匹配相应策略,能够为客户赋能,提供专业的支持和培训等 客户关系维护:与潜在客户和现有客户建立和维护良好的关系,了解机构的需求和反馈,并提供个性化的解决方案。 市场调研:收集市场信息,了解竞争对手的产品和业务策略,为制定有效的业务计划提供支持。 业务报告与分析:定期汇报销售情况,分析数据并提出改进建议,以优化业务流程和策略。 沟通与合作:与内部团队密切合作,包括市场营销、客户服务和供应链团队,确保销售目标的达成。 遵循商业行为准则,合法合理开展业务活动; 完成上级要求的各项任务。 Qualifications: 任职条件: 本科及以上学历,市场营销、医药等相关专业; 三年以上相关领域销售经验;良好的客户管理经验; 良好的人际沟通能力与团队合作精神; 良好的学习及数据分析能力; 具备自我驱动力,能够独立制定工作计划并有效执行; 对护肤品,医疗美容产品及市场趋势有一定了解。 Additional Information: AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html
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Senior Medical Director, Hematology Clinical Development
AbbVie Inc. - Florham Park, NJ, United StatesIndexed from Smartrecruiters Benefit evidence checked May 7, 20266 days agoWhy we showed this
Unspecified Engineering - Staff Plus Resolvable source Verified parental leave: 12 wksource Resolvable source Verified non-birth-parent leave: 12 wksource Salary not disclosed Inferred from posting 401(k) reportedSenior Medical Director, Hematology Clinical Development Florham Park, NJ, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Purpose: Oversees the direction, planning, execution, and interpretation of clinical trials or research activities of one or more clinical development programs. Participates in cross-functional teams to generate, deliver, and interpret high-quality clinical data supporting overall product scientific and business strategy. Responsibilities: Manages the design and implementation of one or more clinical development programs in support of an overall Product Development Plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations, and emerging issues. Oversees project-related education of investigators, study site personnel, and AbbVie study staff. Has overall responsibility for oversight of clinical studies, monitoring overall study integrity, and review, interpretation, and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is responsible for oversight of study enrollment and overall timelines for key deliverables. Responsible for assessment and reporting of serious adverse events per corporate policy and regulations for those protocols on
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Director, External Innovation
AbbVie Inc. - Irvine, CA, United StatesIndexed from Smartrecruiters Benefit evidence checked May 7, 20266 days agoWhy we showed this
Unspecified Other - Staff Plus Resolvable source Verified parental leave: 12 wksource Resolvable source Verified non-birth-parent leave: 12 wksource Salary not disclosed Inferred from posting 401(k) reportedDirector, External Innovation Irvine, CA, United States Company Description: At Allergan Aesthetics, an AbbVie company, we develop, manufacture, and market a portfolio of leading aesthetics brands and products. Our aesthetics portfolio includes facial injectables, body contouring, plastics, skin care, and more. Our goal is to consistently provide our customers with innovation, education, exceptional service, and a commitment to excellence, all with a personal touch. For more information, visit https://global.allerganaesthetics.com/. Follow Allergan Aesthetics on LinkedIn. Job Description: The Director, External Innovation role will report to the Executive Director of External Innovation, Aesthetics. This role will play an integral part in sourcing and evaluation of external innovation opportunities through the leadership and management of commercial assessments related to the TA strategy. This role will support due diligence on deals and driving the Aesthetics business development process internally and externally, targeting licensing/acquisition of key therapeutic assets, R&D collaborations, and related enabling collaborations. Specific activities will include working with the Search & Evaluation and BD&A Transactions teams to evaluate the opportunities, and with the project team to: 1) represent the commercial strategy across all diligence including to senior leaders during governance 2) develop the business development strategy, 3) drive commercial diligence assessment including competitive assessment, 4) product forecasting, and 5) lead commercial P&L generation, and 6) perform market insights generation and gather secondary analytics. The position provides the opportunity to work with a variety of key stakeholders, including but not limited to: Search and Evaluation, Licensing & Acquisition, Clinical, Discovery, Regulatory, Operations, US &
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Untitled role
Truist Financial Corporation - Location not specifiedIndexed from Workday Benefit evidence checked May 7, 20266 days agoWhy we showed this
Unspecified Other - Mid Resolvable source Verified parental leave: 10 wksource Resolvable source Verified non-birth-parent leave: 10 wksource Salary not disclosedUntitled role Location not specified posted:
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Manufacturing Technician I
AbbVie Inc. - Waco, TX, United StatesIndexed from Smartrecruiters Benefit evidence checked May 7, 20266 days agoWhy we showed this
Unspecified Engineering - Mid Resolvable source Verified parental leave: 12 wksource Resolvable source Verified non-birth-parent leave: 12 wksource Salary not disclosed Inferred from posting 401(k) reportedManufacturing Technician I Waco, TX, United States Company Description: About AbbVie Please not this is our B1 Shift: 6am-6:30pm Thursday/Friday/Saturday & every other Wednesday AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Please not this is our B1 Shift: 6am-6:30pm Thursday/Friday/Saturday & every other Wednesday Performs functions associated with cGMP manufacturing operations within the biologics production facility, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components and final materials. Uses sophisticated programs (such as LIMS, SAP, automated control systems, etc.) to collect and evaluate operating data, which can be used to conduct on-line adjustments to products, instruments or equipment. Determines and may assist in developing methods and procedures to control or modify the manufacturing process. Responsibilities Shipping finished materials. Maintaining inventory levels. Sampling of in process and raw materials. Running glass washer / autoclave. Buffer / media preparation. Equipment preparation (CIP / SIP). Cell culture (from vial thaw to production scale). Column chromatography. Tangential flow filtration. Qualifications: High School diploma (or equivalent experience), with 2+
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Schichtleiter Elektro und Mechanik Pharma Produktion (all genders) - Vollzeit, unbefristet
AbbVie Inc. - Ludwigshafen, RP, GermanyIndexed from Smartrecruiters Benefit evidence checked May 7, 20266 days agoWhy we showed this
Unspecified Other - Mid Resolvable source Verified parental leave: 12 wksource Resolvable source Verified non-birth-parent leave: 12 wksource Salary not disclosed Inferred from posting 401(k) reportedSchichtleiter Elektro und Mechanik Pharma Produktion (all genders) - Vollzeit, unbefristet Ludwigshafen, RP, Germany Unternehmensbeschreibung: About AbbVie Herzlich willkommen bei Abbvie! Als Teil eines internationalen Unternehmens mit über 50.000 Mitarbeitern weltweit und rund 3.000 Mitarbeitern in Deutschland hast Du die Möglichkeit, eng mit uns zusammenzuarbeiten, um die gesundheitlichen Herausforderungen von morgen zu meistern. Du hast eine Leidenschaft für die Verbesserung der Gesundheitsversorgung auf der ganzen Welt? Du möchtest Dein Fachwissen einsetzen, um die Lebensqualität von Patienten zu verbessern? In einem herausfordernden Arbeitsumfeld, das Dir die Möglichkeit bietet, Deine eigenen Fähigkeiten zu erweitern und zu entwickeln? Dann bist Du bei uns richtig! Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Stellenbeschreibung: Zur Verstärkung unseres Teams im Bereich Maintenance & Engineering suchen wir einen Schichtleiter Elektro und Mechanik / Supervisor Maintenance (all genders) - Vollzeit, unbefristet . Du führst fachlich und disziplinarisch die Pharma-Techniker mit dem Ziel, die technische Verfügbarkeit der Produktions- und Verpackungsanlagen sicherzustellen. Deine Hauptaufgaben: Fachliche und disziplinarische Führung von Maintenance Mitarbeiter im Schichtbetrieb 24/5 Sicherstellung der fach- und termingerechten Durchführung aller Instandhaltungsmaßnahmen im Bulk-, Verpackungs- und Logistikbereich in Abstimmung mit Produktion und Produktionsplanung Begutachtung und Bewertung elektrotechnischer Tätigkeiten Optimierung der bestehenden vorbeugenden Instandhaltung auf Basis von Analysen der Kennzahlen, Messdaten und Instandhaltungshistorien zur Steigerung der Anlagenverfügbarkeit Durchführen komplexer Entwicklungs- und Optimierungsarbeiten an bestehen Anlagen Durchführung von technischen Risikoanalysen Durchführung und Bewertung von Untersuchungen bei Abweichungen und Complaints Qualifizierung der Mitarbeiter Erstellung von Arbeitsanweisungen zum GMP-gerechten Betrieb Qualifikationen: Das bringst Du mit: Abgeschlossene technische Berufsausbildung (Elektro, Mechatronik,
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Clinical Territory Associate - Future Opportunity
Intuitive Surgical, Inc. - Remote | Memphis, TN, United StatesIndexed from Smartrecruiters Benefit evidence checked May 7, 20266 days agoWhy we showed this
Remote Healthcare - Mid Resolvable source Verified parental leave: 8 wksource Resolvable source Verified non-birth-parent leave: 8 wksource Salary not disclosedClinical Territory Associate - Future Opportunity Remote | Memphis, TN, United States Company Description: At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints. As a pioneer and market leader in robotic-assisted surgery, we strive to foster an inclusive and diverse team, committed to making a difference. For more than 25 years, we have worked with hospitals and care teams around the world to help solve some of healthcare's hardest challenges and advance what is possible. Intuitive has been built by the efforts of great people from diverse backgrounds. We believe great ideas can come from anywhere. We strive to foster an inclusive culture built around diversity of thought and mutual respect. We lead with inclusion and empower our team members to do their best work as their most authentic selves. Passionate people who want to make a difference drive our culture. Our team members are grounded in integrity, have a strong capacity to learn, the energy to get things done, and bring diverse, real world experiences to help us think in new ways. We actively invest in our team members to support their long-term growth so they can continue to advance our mission and achieve their highest potential. Join a team committed to taking big leaps forward for a global community of healthcare professionals and their patients. Together, let's advance the world of minimally invasive care. Job
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Specialty Representative, Psychiatry - Cranberry, PA
AbbVie Inc. - Remote | Cranberry, PA, United StatesIndexed from Smartrecruiters Benefit evidence checked May 7, 20266 days agoWhy we showed this
Remote Sales - Mid Resolvable source Verified parental leave: 12 wksource Resolvable source Verified non-birth-parent leave: 12 wksource Salary not disclosed Inferred from posting 401(k) reportedSpecialty Representative, Psychiatry - Cranberry, PA Remote | Cranberry, PA, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: This role is field-based, and candidates should live within a reasonable distance from the primary city. Talent will be hired at a level commensurate with experience. Execute brand strategy and tactics in field, sales performance, effectively manage assigned territory and targeted accounts, build strong customer relationships and customer needs solving capability to maximize short and long term sales performance placing the patient into the center of any efforts and operating within AbbVie's business code of conduct, policies and all applicable laws and regulations. Responsibilities Deliver sales performance, brand KPIs, financial targets, marketing objectives, etc. to meet or exceed on those objectives. Create pre-call plan objectives and execute post-call evaluation to continuously improve sales performance. Effectively handle objections, misunderstandings, concerns and consistently gain logical and reasonable calls to action to close on every sales call. Proactively and continuously aspire to serve customer needs, customer expectations and challenges to build trusted customer relationships and to achieve win-win agreements
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