Treace Medical Concepts INC jobs

Senior Financial Analyst Ponte Vedra, FL, United States Company Description: Treace's mission is to be the leader in the surgical treatment of bunions by establishing the Lapiplasty® System as the standard of care. We are committed to operating our business with the highest standards of ethical conduct. We intend to exceed our customers' expectations through an innovation-driven, high-velocity approach to solving treatment and surgical problems. With our products and services, our mission is to assist foot and ankle surgeons in improving patient outcomes and reducing healthcare costs, while providing rewarding experiences and opportunities for our employees and stakeholders. Job Description: We are currently seeking a talented and detail-oriented Senior Financial Analyst to join our team. The ideal candidate will support our financial planning, analysis, and reporting processes and work closely with our Senior Finance Manager for FP&A. This is an excellent opportunity to contribute to our organization by delivering accurate and timely month-end reporting, variance analysis, and participating in annual operating activities. Primary Duties and Responsibilities Prepare monthly, quarterly, and annual corporate reports summarizing financial results and key performance metrics. Organize data from multiple sources to ensure timely analysis and accurate payouts. Assist with financial planning, including executing annual planning processes, forecasting, and capital budgeting. Perform financial modeling and maintain data sources to support organizational decision-making. Identify and drive process improvements by developing standard and ad-hoc analytics, reports, and tools. Participate in a variety of cross-functional projects and collaborate closely with other departments. Conduct ad hoc analysis as needed to

Senior Medical Science Liaison (multiple territories) United States Position Overview The Senior Medical Science Liaison (MSL) role is the field-based medical/scientific expert for the company, focusing on engagement with healthcare providers to provide fair/balanced education on investigational products, understanding the evolving therapeutic landscape, and supporting research collaborations across the portfolio. We are building our Field Medical team and are open to hiring in multiple territories for qualified candidates. Responsibilities - Identifies, establishes, and maintains collaborative relationships with key investigators, institutions, groups and consortia in disease state areas of strategic focus for the company. - Provides education to the medical community on the company's investigational products and disease areas of focus. - Increases company visibility and enhances professional interaction with current and future oncology leaders. - Participates in medical education for healthcare professionals, including formulary (P&T) committees, through presentations at appropriate venues. - Works with the appropriate departments/personnel at clinical sites to ensure required education and training are provided as needed. - Identifies clinical research opportunities that are consistent with company objectives. - Is the primary territory contact for the investigator-initiated research program, facilitating the process from concept submission through publication. - Identifies and communicates key clinical and research insights from oncology leaders to help shape company research. - Maintains a high level of clinical and scientific expertise through ongoing training and self-education, including attendance of relevant conferences, scientific workshops, and review of key publications. - Gathers and disseminates competitive intelligence in a compliant manner. - Takes advantage of opportunities to

Medical Science Liaison / Senior Medical Science Liaison (Midwest) Medical Science Liaison / Senior Medical Science Liaison (Midwest)

Medical Science Liaison Director/Lead Viking Therapeutics, Inc. Medical Science Liaison Director/Lead

Medical Affairs Oncology Medical Advisor (M.D.) JPN - Tokyo - Chiyoda posted: Posted 30+ Days Ago

(Medical Oncology) Field Medical Director, Oncology Work at Home posted: Posted 14 Days Ago

Lead Designer, Brand Concepts Global - Converse Boston, Massachusetts posted: Posted 30+ Days Ago

Medical Affairs Medical Review Sr. Specialist JPN - Tokyo - Chiyoda posted: Posted 3 Days Ago

Medical Affairs Manager Medical Devices (m/f/d) Berlin, Germany posted: Posted 30+ Days Ago

Oncology Medical Director, Medical Oncology Performance Work at Home posted: Posted 14 Days Ago

Medical Director (Medicare) United States Medical Director (Medicare)

Area TA Lead (Director) Neuroscience, Intercontinental Medical Affairs Mettawa, IL, United States Company Description: 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 - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: The Area TA Lead will act as the Intercontinental Neuroscience Lead, providing medical/scientific strategic and operational input into core medical affairs activities and relevant scientific and technical training to Affiliate Therapeutic Area resources. Will work closely with Area commercial teams to provide strategic medical input into core Neuroscience assets strategies, and to support medical/marketing activities and market access; provide scientific and technical support for assigned products. Develops and maintains professional and credible relationships with key external experts and professional societies; provides therapeutic expertise in interactions with regulators and other external groups; develops innovative research concepts for clinical data generation and communication. Collaborates with clinical development, global, International teams, and affiliates to support pipeline execution and acceleration efforts across Intercontinental geographies for neuroscience assets. *Hybrid (3x per week on-site) in Mettawa, IL. Key Responsibilities Include : Develops Area therapeutic Evidence Generation plan and Area therapeutic strategic initiatives Brings insights and knowledge from

Senior Software Quality Engineer Tijuana, Mexico Company Overview Join us for an enriching journey with Outset, a trailblazing medical device company that is revolutionizing the field of dialysis. Our focus is to create one high performing team, obsessed with progress, in an atmosphere that is brimming with transformative opportunities. The heart of our mission is pioneering a groundbreaking technology that redefines the landscape of dialysis, streamlining complexity and cost, because patients deserve “better” now, not some day. At Outset we're revolutionizing an industry and changing lives. We're impacting what the future of dialysis looks like by creating a first-of-its-kind technology in order to reduce the cost and complexity of dialysis. FDA cleared for use across care settings, from the hospital to the clinic to the home, the Tablo® Hemodialysis System harnesses modern technology for a new holistic approach to dialysis care. We're giving providers time back to focus on patient care. And we're giving patients the power to take control of their life and get back to enjoying the things they love. Position Overview: The Senior Software Quality Engineer is responsible for performing design assurance activities for new introductions and sustaining of medical device software, with the purpose of supporting the Software R&D, Test and Manufacturing departments. The incumbent for this position will support the Software Development Lifecycle of one or more projects from concept generation through production. This person will work closely with software design, software testing, project management, product management, regulatory, human factors, and manufacturing teams to understand

Manager, Stores Concepts & Operations Enablement - Converse Shanghai, China Mainland posted: Posted 30+ Days Ago

Senior / Medical Director Cambridge, MA The Opportunity: As a Senior / Medical Director at Relay Tx, you will help advance our clinical pipeline from IND to proof of concept to registration. Specifically, you will collaborate with senior medical staff to drive clinical strategy, clinical trial design, and execution. Working cross-functionally with clinical project management, regulatory affairs, clinical operations, biostatistics, data management and medical writing, you will play a key role as Relay Tx continues to introduce product candidates into the clinic. You will provide clinical leadership to R&D teams and will work closely with Development leadership. We are open to remote employees About You: - Collaborate with senior medical staff, drug discovery teams, translational oncology, clinical operations, clinical investigators and disease-specific experts to design and execute early clinical development plans that definitively test key translational hypotheses for Relay Tx medicines and establish clinical proof-of-concept as soon as possible after entering human testing. - Write clinical sections of key documents, including Investigator's Brochures, IND summary documents, CTAs for initiation of ex-US studies and work with senior medical staff for responses to questions from regulatory authorities, IRBs, and ethics committees. - Provide expert medical review, assessment, and interpretation of clinical data and prepare results for presentation to internal clinical development leadership and external stakeholder including regulatory authorities. - Manage drug safety and pharmacovigilance activities for ongoing trial(s). - Attend and support clinical site initiation visits. - Rapidly integrate new insights derived from on-going Relay Tx or external clinical trials, translational science

Scientific Director, Medical Affairs Boston, Massachusetts Scientific Director, Medical Affairs

Project Manager (Medical Device, New Product Development) Cincinnati, Ohio, United States of America Embrace the opportunity to become a Project Manager (Medical Device, New Product Development) and lead innovative projects in life sciences and diagnostics. Drive cross-functional teams, manage schedules and budgets, and ensure successful product launches from concept to completion. Make a real impact in healthcare with a company committed to continuous improvement and patient care.

Director, Medical Affairs Germantown, MD, US Director, Medical Affairs

Alternance Qualité Conception et Laboratoires R&D H/F FRA - Brittany - Vitre posted: Posted 30+ Days Ago

Medical Affairs Lead - Osteoarthritis NYC, NY; Boston, MA About Formation Bio Formation Bio is a tech and AI driven pharma company differentiated by radically more efficient drug development. Advancements in AI and drug discovery are creating more candidate drugs than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of new medicines that can reach patients, Formation Bio, founded in 2016 as TrialSpark Inc., has built technology platforms, processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines to patients. The company is backed by investors across pharma and tech, including a16z, Sequoia, Sanofi, Thrive Capital, John Doerr, Spark Capital, SV Angel Growth, and others. You can read more at the following links: - Our Vision for AI in Pharma - Our Current Drug Portfolio - Our Technology & Platform At Formation Bio, our values are the driving force behind our mission to revolutionize the pharma industry. Every team and individual at the company shares these same values, and every team and individual plays a key part in our mission to bring new treatments to patients faster and more efficiently. About the Position The Medical Affairs Lead is a first-in-function leadership role responsible for building an AI-native Medical Affairs capability across

Senior Account Manager- Medical Devices City Remote Employee US | State/Province New Hampshire | Country USA Req ID: 137305 Remote Position: Region: Country USA Summary Celestica is dedicated to delivering end-to-end product lifecycle solutions to drive our customers' success. Our growing Advanced Technology Solutions (ATS) organization focuses on applying Celestica's advanced capabilities, knowledgeable people and innovative tools to enable companies in the medical device industry with highly complex, mission critical applications to improve their competitive advantage. We are currently expanding our Advanced Technology Solutions (ATS) account management organization and are seeking a senior account manager to join our corporate healthtech team and shape the future of a collaborative, high performance, growth oriented business unit. Detailed Description At Celestica, our people make the difference… We are looking for a Senior Account Manager with experience working with OEMs; a leader with a deep knowledge and experience in medical device manufacturing as well as customer relationships. If you are a highly motivated individual interested in becoming a key player into the fast growing medical device sector, we want you on our team. The successful candidate will take the challenge of joining a fast growing segment within Celestica, partnering with global leading Medical Device OEM´s managing projects from design conception to manufacturing, offering full solutions to our global customers. As Account Manager, you will… Support regional account/site strategies to support and enhance th

Senior/Executive Medical Director, Clinical Development (New Indications) South San Francisco Alumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases. Even with treatment innovations of the last two decades, many patients with immunologic conditions continue to suffer - our goal is to fundamentally change the outcomes for these patients. Alumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases. Even with treatment innovations of the last two decades, many patients with immunologic conditions continue to suffer - our goal is to fundamentally change the outcomes for these patients. Position Summary Alumis is seeking an experienced Executive Medical Director or Senior Medical Director to lead clinical development strategy and execution for Phase 1 and Phase 2 studies evaluating envudeucitinib and A-005 across new indications identified for expansion of the Alumis pipeline. This high-impact role will be instrumental in shaping the company's clinical development portfolio, from indication selection through proof-of-concept studies, and will serve as a key scientific leader interfacing with internal teams, regulatory authorities, and the external medical community. --- Key Responsibilities Clinical Development Strategy & Leadership · Lead the design, planning, and execution of Phase 1 and Phase 2 clinical studies for A-005 and additional pipeline molecules in new therapeutic indications · Develop and refine clinical development plans, including study synopses, protocols, and integrated development strategies for new indications · Provide clinical and scientific leadership to cross-functional study teams, ensuring alignment on

Senior System Verification Engineer (Medical Device) Stockholm, Sweden Mission Neko is redefining what prevention means, from treating illness when it arrives, to sustaining health before it's ever at risk. Our mission: make data-driven, preventative care accessible to more people, before symptoms appear. In a single, non-invasive visit under an hour, proprietary technology and direct clinical care combine to deliver personalised, actionable insights. It's a team that thinks in 10x, not 10%. Every role here plays a part in building a world where prevention is the norm, and where your work genuinely helps people live longer, healthier lives. Neko Health is a Swedish healthcare technology company co-founded in 2018 by Hjalmar Nilsonne and Daniel Ek. Neko's vision is to shift healthcare from reactive treatment toward preventative health and early detection. This requires completely reimagining the patient's experience and incorporating the latest advances in sensors and AI. Neko Health has developed a new medical scanning technology concept to make it possible to do broad and non-invasive health data collection that is convenient and affordable for the public. The company is based in Stockholm, offering the Neko Body Scan experience at locations in Stockholm, London and Manchester, with over 500 employees. We are currently seeking a Senior System Verification Engineer to join our multidisciplinary engineering team. In this role, you will take ownership of system-level verification activities across the product lifecycle, from early concept through industrialization and market release. You will work closely with hardware, firmware, and software teams to ensure our medical

Clinical Informaticist BENGALURU, KARNATAKA, India, IN We are seeking a Clinical Informaticist to join our dynamic team at Oracle America, Inc. In this role, you will play a crucial part in our Oracle Health Prod Mgmt - Data Prediction department, ensuring the accuracy and integrity of medical annotations. Your clinical expertise and attention to detail will be instrumental in supporting our AI/ML and healthcare data projects, contributing to the development of innovative healthcare solutions. Required Experience Clinical experience or education in nursing, medicine and surgery, pharmacy, laboratory sciences, respiratory therapy, health information management, medical coding, or another healthcare-related field. 0-2 years of experience in healthcare, clinical operations, medical coding, quality assurance, healthcare technology, or related healthcare environments. Familiarity with clinical documentation and healthcare terminology. Basic understanding of healthcare workflows and patient care processes. Ability to accurately interpret clinical documentation and healthcare concepts Strong attention to detail and commitment to quality. Demonstrated ability to learn new systems, processes, and technologies. Demonstrated understanding of the US healthcare system Preferred Experience Exposure to data annotation, quality assurance, healthcare analytics, AI/ML, NLP, or healthcare technology projects. Exposure to electronic health record (EHR) systems. Experience reviewing healthcare records, quality measures, clinical documentation, or medical coding. Familiarity with healthcare terminologies such as ICD, CPT, SNOMED CT, LOINC, or RxNorm. Bachelor's degree in a healthcare, life sciences, health informatics, or related field preferred. Perform medical annotations following established guidelines, ensuring accuracy and consistency. Review annotations for quality, identifying and addressing any discrepancies. Conduct quality assurance checks on