FewerJobs.
Employers

Employer profile

Crinetics Pharmaceuticals INC

36 open roles indexed with location, benefit, and apply-link signals where available.

ATS: workday

Open roles

Showing the most recent indexed roles for this employer.

Search all matching jobs

  • Clinical Trial Manager

    Remote

    remote $122K-$152K

    Clinical Trial Manager Remote Position Summary: The Clinical Trial Manager is responsible for managing the execution of clinical studies and data collection. The incumbent oversees the review, monitoring and adherence to clinical protocols, as well as fulfilling activities related to study completion. The Clinical Trial Manager will interact internally and externally with members of the cross-functional study team. Essential Job Functions and Responsibilities: These may include but are not limited to: Provide oversight of clinical research studies across all functional areas of the drug development process. Provide operational and strategic input into study documents such as synopsis, protocol, ICF, CRFs, CRF Completion Guidelines, Study Execution Plans, Clinical Data Review Plan, Clinical Database edit specifications, Clinical Study Report (CSR) development, etc. Develop the subject recruitment/retention strategy and related initiatives. Oversight of TMF set-up, ongoing quality review, and final reconciliation of study documents including review of site regulatory documents/packages and obtaining of appropriate site insurance, and/or supervision of team members performing these activities. Development of training materials for study team, investigational sites, and vendors. Proactive management of information sharing with key stakeholders using standardized reports and other mechanisms. Assure clinical studies are compliant with ICH/GCP and other regulations as appropriate. Oversee preparation of RFPs and prepare bid templates to facilitate selection of the CROs/vendors, and/or collaboration/supervision with team members performing these activities. Collaborate with counsel to negotiate and draft research contracts and agreements with CROs/vendors and clinical study sites, as needed. Acts as liaison with Regulatory Affairs to assure adherence to GCPs;

  • Manager, Clinical Business Operations

    Remote

    remote $132K-$165K

    Manager, Clinical Business Operations Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The Manager, CBO will support the AD, CBO with the internal growth of the newly formed CBO pillar under the Outsourcing and Vendor Governance (OVG) department. This role will primarily develop and negotiate US site budgets for Crinetics' late phase clinical trials. Strong negotiation and cross-functional relationship skills are key to this position. This role will also provide input into developing processes, various trackers, and metrics reporting for CBO. Essential Job Functions and Responsibilities: These may include but are not limited to: Develop, negotiate and execute site budgets and ensure consistency among sites with multiple Crinetics' studies Close collaboration with global CRO partners on the site budget template development and

  • Associate Director, Regulatory Affairs CMC

    Remote

    remote $150K-$194K

    Associate Director, Regulatory Affairs CMC Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully-integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The Associate Director, Regulatory Affairs CMC will be responsible for supporting regulatory strategy implementation for development programs. Works closely with the Senior Director, Regulatory Affairs CMC to lead and prepare regulatory submissions (authoring, timeline planning, etc.), to support regulatory and clinical objectives. Assists in developing and implementing global regulatory strategies. Establishes and maintains department regulatory processes. The individual is responsible for developing collaborative and productive partnerships internally, as well as externally with contract research organizations, electronic publishing, and other vendors as required. Essential Job Functions and Responsibilities: These may include but are not limited to: Actively participate as a member of Regulatory Affairs teams and on cross-functional product development teams as needed. Contribute to developing and implementing regulatory strategies for global

  • Senior Medical Director, Clinical Research, Endocrinology

    Remote

    remote $330K-$362K

    Senior Medical Director, Clinical Research, Endocrinology Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully-integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The Senior Medical Director, Clinical Research will be working within a multi-disciplinary team and will be accountable for developing the strategy and the Clinical Development Plan for one or more indications for a specific Crinetics' compound. The incumbent will have hands-on responsibility designing, executing, and analyzing clinical trials. The incumbent will have a key role in the understanding and interpretation of the results from these studies as well as the preparation of the summary documents needed for a global submission to regulatory authorities. Essential Job Functions and Responsibilities: These may include but are not limited to: Clinical leader of one or more endocrinology programs, being integral to developing the

  • Manager, Trial Disclosure, Medical Writing Operations

    Remote

    remote $130K-$154K

    Manager, Trial Disclosure, Medical Writing Operations Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The Manager of Medical Writing Operations - Trial Disclosure role is responsible for clinical trial transparency and disclosure activities, including initial trial postings, results postings, document redaction, and plain language summary development. The role is responsible for ensuring accurate and compliant public release of clinical trial information while working in close collaboration with cross-functional teams. This role is also responsible for redacted documentation in accordance with company confidential information (CCI) and the General Data Protection Regulation. Essential Job Functions and Responsibilities: These may include but are not limited to: Ensure company compliance with clinical trial transparency laws and requirements by applying expert knowledge of key regulatory frameworks, including

  • Senior Director, Clinical Science

    Remote

    remote $250K-$287K

    Senior Director, Clinical Science Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully-integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The Senior Director, Clinical Science will be working within a multi-disciplinary team and leading a group of Clinical Scientists implementing Endocrine Clinical Development programs. This individual will provide clinical expertise and scientific insights to clinical development activities (phase 1 - 3 studies), including regulatory documents. The incumbent will collaborate with all the groups involved in Clinical Development e.g., Clinical Pharmacology (CP), Clinical Operations, Medical Writing, Biometrics, Pharmacovigilance, Regulatory Affairs, HEOR and Medical Affairs. Essential Job Functions and Responsibilities: These may include but are not limited to: Lead and mentor the Clinical Scientist team (including consultants), reviewing their work and supporting their professional development. Serve as a scientific liaison between clinical research

  • Senior Clinical Scientist

    Remote

    remote $180K-$210K

    Senior Clinical Scientist Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully-integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The Senior Clinical Scientist will be working within a multi-disciplinary team focusing on a Clinical Development Program. This individual will provide clinical expertise and scientific insights to help monitor, track, and analyze subjects' data in phase 1 - 3 studies. The incumbent will work closely with the Medical Lead and will collaborate with all the groups involved in Clinical Development e.g., Pharmacokinetics (DMPK), Clinical operations, Biometrics, Pharmacovigilance, and Medical Affairs. Essential Job Functions and Responsibilities: These may include but are not limited to: Responsible for monitoring, tracking, and analyzing clinical trials subjects' data, under the supervision of the Clinical Medical Lead. This involves collaborating with investigators, CRO medical monitors, Clinical Operations and

  • Director, Omnichannel Marketing

    Remote

    remote $181K-$226K

    Director, Omnichannel Marketing Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully-integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The Director, Omnichannel Marketing will play a critical role in designing, executing, and optimizing integrated omnichannel strategies that engage patients, healthcare professionals, and other key stakeholders across the customer journey. This role will lead the development of cohesive, data-driven experiences across digital, non-personal, and personal channels, ensuring consistent messaging, optimal channel mix, and measurable impact. The Director will be responsible for building and scaling omnichannel capabilities, partnering closely with brand, analytics, IT, commercial operations, and agency partners to drive short-term execution while establishing sustainable mid- to long-term omnichannel excellence. This role ensures all initiatives are executed in compliance with company policies and applicable regulatory requirements. Essential Job Functions and Responsibilities: These may

  • Senior Director, Global Privacy

    Remote

    remote $216K-$270K

    Senior Director, Global Privacy Remote Position Summary: Crinetics is seeking a highly experienced and strategic Senior Director, Global Privacy to provide enterprise-level leadership of the company's global privacy and data protection. Reporting to the VP, Global Compliance, this role serves as a senior legal and strategic advisor responsible for advancing privacy governance and strategy while managing complex privacy risk across clinical development, research pharmacovigilance, and commercial operations. This position plays a critical role in scaling and maturing the privacy function, including oversight of policies, controls, third-party risk, incident response, and regulatory change management. The role requires significant independent judgment, cross-functional leadership, and the ability to influence and guide senior leaders through complex privacy, cybersecurity, and data-use issues in a public-company pharmaceutical environment. Essential Job Functions and Responsibilities: These may include but are not limited to: Lead the design, implementation, and ongoing enhancement of Crinetics' global privacy and data-protection program, including the design, implementation, and ongoing oversight of policies, standards, procedures, and controls aligned with U.S. and international privacy laws and industry best practices. Establish and chair enterprise privacy and data-governance forums, defining decision rights, escalation pathways, and accountability across functions. Provide regular executive-level reporting on privacy risk posture, program effectiveness, and emerging regulatory developments. Serve as the company's senior legal authority on privacy, data protection, and data-use governance, advising executives and cross-functional leaders on risk-based, compliant approaches to business initiatives. Translate complex legal requirements into practical operating guidance that supports innovation, patient trust, and responsible data use. Provide senior-level oversight

  • Senior Director, Clinical Pharmacology

    Remote

    remote $238K-$297K

    Senior Director, Clinical Pharmacology Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully-integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The Senior Director, Clinical Pharmacology will be a key member of the development team, developing clinical pharmacology strategy suitable for target product profile (TPP) and clinical development plan (CDP), leading the design, execution, interpretation and reporting of Phase 1 clinical pharmacology studies, and serve as clinical pharmacology lead on studies and project teams. The work will support projects at various stages of development thereby allowing the selected candidate to play an active role in our drug discovery and development efforts to advance small molecule therapeutics for rare endocrine disorders and endocrine-related cancers. Essential Job Functions and Responsibilities: These may include but are not limited to: Develop clinical pharmacology strategy and related

  • Senior Manager, Clinical Data Management - External Data Management

    Remote

    remote $138K-$172K

    Senior Manager, Clinical Data Management - External Data Management Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully-integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The Senior Manager, Clinical Data Management - External Data Management (CDM‑EDM) is a hands‑on, individual contributor role responsible for executing and owning external (non‑EDC) data management activities for assigned clinical studies. This position focuses on direct execution and plays a critical role in ensuring external vendor data are timely, high quality, inspection‑ready, and fit for statistical analysis and regulatory submission. The role partners closely with external vendors, CROs, and internal cross‑functional stakeholders to set up data transfer agreements (DTAs), validate test files, manage ongoing data transfers, and perform data reconciliation and quality control activities in compliance with ICH‑GCP, 21 CFR Part 11, and internal SOPs. Essential

  • Contract Manager

    San Diego, CA

    unspecified $109K-$136K

    Contract Manager San Diego, CA Position Summary: The Crinetics Legal Team is seeking an experienced Contracts Manager to support Technical Operations (formerly CMC) and broader G&A functions. This role serves as a key business partner to Technical Operations, enabling efficient, compliant, and scalable contracting across development, manufacturing, supply chain, and quality operations. This individual will manage a high volume of contracts with external partners, including Contract Manufacturing Organizations (CMOs), Contract Development and Manufacturing Organizations (CDMOs), suppliers, and service providers. Core responsibilities include drafting, reviewing and negotiating a range of agreements, including but not limited to Master Service Agreements (MSAs), Statements of Work (SOWs), supply and technical services agreements, consulting agreements, and related amendments and change orders. In addition to contract execution, this role will play a critical part in supporting and enabling business stakeholders, including guiding end users through the contract intake process, improving submission quality, and providing training on contracting processes and tools (e.g., Ironclad CLM). The role will also support contract processes tied to GxP compliance, regulatory inspections, and product lifecycle activities, ensuring alignment with company policies and regulatory requirements. This position will contribute to the ongoing maturity and optimization of the end-to-end contracting lifecycle, including process improvements, template standardization, and stakeholder enablement. Essential Job Functions and Responsibilities: These may include but are not limited to: Lead the preparation, review, and negotiation of contracts, ensuring all key terms, including scope, deliverables, milestones, timelines, and termination provisions, are clearly defined, accurately tracked, and aligned with business objectives. Partner cross-functionally

  • Director, Patient Marketing

    Remote

    remote $193K-$241K

    Director, Patient Marketing Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The Director, Patient Marketing, will be instrumental in crafting and implementing strategies and tactics tailored to the rare disease community. Your responsibilities will include spearheading a range of initiatives, from near-term execution to developing new capabilities for mid-to-long-term brand success. This encompasses managing educational initiatives, cultivating relationships with key opinion leaders, and ensuring all marketing initiatives for patients and healthcare professionals adhere to company compliance standards. Essential Job Functions and Responsibilities: These may include but are not limited to: Develop comprehensive patient-centric strategies across multiple disease states including understanding the patient journey, identifying unmet needs, developing innovative solutions, and executing programs to meet those needs. Lead patient ambassador programs to include

  • Senior Accountant 1

    Remote

    remote $83K-$104K

    Senior Accountant 1 Remote Position Summary: The Senior Accountant 1 is responsible for helping to ensure the accuracy, completeness and appropriateness of general ledger transactions in accordance with US GAAP. Requires the ability to read and interpret contractual terms to ensure all costs associated with contractual commitments are recorded in the financial statements during the appropriate accounting period. This position will participate in a variety of financial functions including month-end closing, financial reporting and other administrative functions. Areas of responsibility will typically be in most challenging areas of the Company's accounting, including R&D accruals. A SOX-compliant mindset, strong, proactive, analytical, and problem-solving skills, and desire and ability to identify, recommend and lead improvements is important. Other duties include reviewing coding on invoices, maintaining banking records, reconciling BS schedules, and miscellaneous accounting and administrative duties . Essential Job Functions and Responsibilities: These may include but are not limited to: Support month-end close process, including data entry, reconciliation of sub-ledgers to the general ledger, and maintenance of balance sheet account reconciliations Prepare G&A, and select R&D accruals, including maintaining trackers, coordination with functional leaders and analyzing other accruals for accuracy and completeness Assist with operationalizing contract terms and ensuring appropriate accounting treatment in accordance with guidance assessed by the SEC & Technical Accounting team Manage prepaid reconciliations, including subscriptions, insurance and other prepaid accounts Oversee fixed asset accounting including additions, disposals, depreciation, and execution of the annual fixed asset inventory Prepare and record payroll‑related journal entries and partner closely with the Payroll

  • Senior Clinical Research Associate

    Remote

    remote $119K-$149K

    Senior Clinical Research Associate Remote Position Summary: The Senior Clinical Research Associate (Sr. CRA) will participate in the preparation and execution of Phase 1-3 clinical trials. The Sr. CRA oversees the progress of clinical investigations by conducting site qualification, initiation, interim, and close-out visits. The Sr. CRA monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by Crinetics Pharmaceuticals and partner CRO(s). The Sr. CRA works closely with the Clinical Trial Manager (CTM) and Clinical Monitoring management to ensure all monitoring activities are conducted according to study requirements. The Senior CRA may also participate in monitoring oversight activities such as CRO oversight visits, internal CRA training and evaluation visits, and CRO monitoring visit report review. Essential Job Functions and Responsibilities: These may include but are not limited to: Develop strong, collaborative investigational site relationships and ensure continuity of relationships through all stages of the trial. Perform clinical study site management/monitoring activities efficiently in compliance with GCP/ICH requirements, SOPs, local laws and regulations, protocol, Clinical Monitoring Plan, and associated documents. Participate and provide input on site selection and site qualification activities. Coordinate and manage assigned tasks in collaboration with the study team to achieve site activation. Perform remote and on-site monitoring activities using various tools to ensure subject rights, safety and well-being are protected as well as the reliability and integrity of study data. Conduct site visits including but not limited to qualification visits, initiation visits, interim monitoring visits, and close-out visits; generate clear, comprehensive, and accurate

  • Director, Program Management

    Remote

    remote $186K-$233K

    Director, Program Management Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The Director, Program Management is a leadership role responsible for driving cross-functional execution and providing strategic operational leadership for Crinetics' drug development programs. As a senior member of the Program and Portfolio Management organization, this role serves as a strategic partner to the Program Global Product Leader (GPL), translating program strategy into integrated, executable plans and enabling timely, high-quality decision-making across a complex matrix. The Director owns the integrated program plan and critical path across one or more programs, leads program operating rhythms and governance forums, and proactively identifies risks, interdependencies, and tradeoffs across timeline, scope, and resourcing. The role provides clear, executive-ready visibility into program status, decisions, and delivery implications

  • Director, Quality Systems, Project Management, QRM, RS

    US California

    unspecified $178K-$223K

    Director, Quality Systems, Project Management, QRM, RS US California Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully-integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: We are seeking a highly skilled Director of Quality Systems with a focus on Project Management, Quality Risk Management (QRM), and Regulatory Surveillance to join our Quality team. This role will be instrumental in managing QA projects, implementing risk management strategies and tools, and ensuring adherence to cGMP regulations and global pharmaceutical quality standards. The ideal candidate brings cross-functional leadership, regulatory knowledge, and strong analytical capabilities to support our commitment to patient safety and product integrity. This role is also responsible for developing collaborative and productive partnerships internally, as well as externally with Global sites and strategic partners. Essential Job Functions and Responsibilities: These may include but

  • Associate Manager, Centralized Monitoring

    Remote

    remote $115K-$144K

    Associate Manager, Centralized Monitoring Remote Position Summary: The Associate Manager, Centralized Monitoring is responsible for executing and overseeing centralized monitoring activities across clinical trials using a risk-based quality management (RBQM) framework. The role focuses on proactive signal detection, data surveillance, risk identification support, and escalation to support study quality, participant safety, and regulatory compliance. This position also contributes to process improvement, and cross-functional collaboration related to centralized monitoring activities. Incumbent will support cross-functional collaboration across multiple clinical studies, with a focus on regulatory compliance and inspection readiness. Essential Job Functions and Responsibilities: These may include but are not limited to: Support the execution of centralized monitoring strategies for studies ensuring setup aligns with Crinetics' RBQM best practices. Perform ongoing centralized monitoring reviews using clinical, operational, and quality data sources (e.g., EDC, CTMS, safety, vendor data). Identify emerging study-level and site-level risks through Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), and analytical outputs. Support the evaluation of trends, data anomalies, protocol deviations, and performance metrics to detect potential quality or compliance issues. Document and report signals, findings, and recommendations within designated systems (e.g., CTMS, RBQM platform). Support study teams' understanding of the significance and root causes of centralized monitoring findings. Contribute to the development and maintenance of RBQM documentation, including: Centralized Monitoring Plans KRI and QTL threshold definitions SDV and SDR strategies Collaborate with Clinical Monitoring to support alignment of monitoring approaches with ICH-GCP E6 (R2/R3) and internal SOPs. Provide input on targeted monitoring actions, such as focused SDV, site

  • Director, Global Product Leader

    Remote

    remote $187K-$233K

    Director, Global Product Leader Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully-integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: This position will lead several early or one late-stage development programs and contribute to portfolio strategy for other programs within a growing preclinical and clinical stage pipeline covering endocrinology and endocrine related tumors. The Director, Global Product Leader is responsible for the strategic leadership of a Global Product Team, overseeing strategic planning, decision making, and resource/budget management and prioritization across development, regulatory, CMC, operations, and business functions to ensure rapid, efficient, and successful progression of the program(s). This role will be responsible for the full lifecycle management of their product and ensure that strategic plans and goals are met. The Global Product Leader will ensure cross-functional and organizational readiness for regulatory

  • Senior Contracts Manager

    Remote

    remote $125K-$156K

    Senior Contracts Manager Remote Position Summary: The Senior Contracts Manager is responsible for comprehensive support of the organization's commercial and general and administrative (G&A) contracting program, including the review, drafting, negotiation, and administration of a broad range of commercial and operational agreements. These include master services agreements, confidentiality agreements, consulting agreements, statements of work, and related contracts. In addition to contract execution, this role contributes to the development and ongoing maturation of contracting processes, templates, and workflows, partnering closely with Commercial, Medical Affairs, Finance, Procurement, and other stakeholders to ensure contracts strategically support the business needs. Work can be based at Crinetics' headquarters in San Diego or remote. Essential Job Functions and Responsibilities: These may include but are not limited to: Collaborate with Compliance and other internal stakeholders to implement and manage documentation and administrative processes for review and approval of Commercial, Legal, Compliance and Medical Affairs activities under the direction of Executive Director & Associate General Counsel, Commercial Legal. Support Commercial and Medical Affairs initiatives through ad hoc legal research, cross-functional collaboration, and other related responsibilities, as assigned. Draft, review, negotiate, and execute a broad range of contracts supporting diverse business transactions. Lead contract negotiations, including reviewing and coordinating stakeholder input on redlines to ensure appropriate review and approval by business, Finance, Compliance, IP, and other relevant partners. Ensure contractual terms and conditions are consistent with Crinetics policies, standards, and established guidance. Exercise sound judgment to identify contract issues, decisions, or other matters impacting agreements that require escalation, and