The Clinical Scientist provides scientific expertise to develop protocols for phase 1-3 studies and monitors subject data. They collaborate across multi-disciplinary teams to conduct data analyses and contribute to regulatory documents and clinical development plans.
Crinetics Pharmaceuticals
18 Remote Job Openings at Crinetics Pharmaceuticals
Responsible for ensuring the accuracy of general ledger transactions and managing month-end closing processes in accordance with US GAAP. Key duties include handling R&D accruals, fixed asset accounting, and maintaining SOX compliance.
Field Reimbursement Liaison - Northeast
Crinetics Pharmaceuticals
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Full Time
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5 days ago
Crinetics Pharmaceuticals
The Field Reimbursement Liaison provides access and reimbursement assistance to optimize the patient experience for endocrine therapies. This involves educating healthcare professionals on patient programs and coordinating with cross-functional teams to resolve complex coverage and denial issues.
Senior Manager, Clinical Data Management - External Data Management
Crinetics Pharmaceuticals
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Full Time
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5 days ago
Crinetics Pharmaceuticals
The role is responsible for executing and owning external non-EDC data management activities, including the development of Data Transfer Agreements and data reconciliation. It involves partnering with vendors and cross-functional teams to ensure high-quality, inspection-ready data for regulatory submissions.
Clinical Project Manager
Crinetics Pharmaceuticals
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Full Time
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7 days ago
Crinetics Pharmaceuticals
The Clinical Project Manager is responsible for managing timelines and budgets for clinical studies while partnering with cross-functional stakeholders. Key duties include financial oversight, risk mitigation, and coordinating study milestones to ensure successful trial delivery.
Senior Manager, Clinical Systems and Processes
Crinetics Pharmaceuticals
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Full Time
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7 days ago
Crinetics Pharmaceuticals
Lead the design, implementation, and continuous improvement of clinical systems including Veeva Vault and RBQM frameworks. Provide oversight for system validation, vendor governance, and organizational change management to ensure GxP and 21 CFR Part 11 compliance.
Clinical Trial Associate
Crinetics Pharmaceuticals
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Full Time
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12 days ago
Crinetics Pharmaceuticals
The CTA supports the study team by executing study activities according to protocols and regulatory guidelines across investigator sites. Key duties include maintaining the Trial Master File, coordinating regulatory documents, and assisting with project management tasks from inception to database lock.
Senior Manager, Quality Assurance GCP
Crinetics Pharmaceuticals
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Full Time
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13 days ago
Crinetics Pharmaceuticals
Manage and conduct GCP and GLP qualification and routine vendor audits while maintaining annual audit programs and trackers. Provide quality oversight for clinical study documents and support regulatory inspection readiness and compliance programs.
Sr. Research Associate, Drug Product Development
Crinetics Pharmaceuticals
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Full Time
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19 days ago
Crinetics Pharmaceuticals
Support the development of drug product formulations from preclinical studies through clinical supply for First-in-Human trials. This includes hands-on laboratory execution, stability testing, and preparing CMC documentation for regulatory submissions.
Associate Director, Clinical Project Management
Crinetics Pharmaceuticals
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Full Time
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20 days ago
Crinetics Pharmaceuticals
Oversee clinical project management activities including timelines, budgets, and risk management for multiple studies and molecules. Lead and mentor a team of Clinical Project Managers while streamlining processes and coordinating with finance and portfolio management.
Senior Manager, Clinical Trial Supplies
Crinetics Pharmaceuticals
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Full Time
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a month ago
Crinetics Pharmaceuticals
Responsible for the planning, execution, and oversight of global clinical trial supply operations across multiple programs. This includes managing the end-to-end lifecycle of investigational products, from forecasting and packaging to distribution and destruction.
Senior Director, Clinical Pharmacology
Crinetics Pharmaceuticals
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Full Time
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a month ago
Crinetics Pharmaceuticals
The Senior Director will develop clinical pharmacology strategies and lead the design, execution, and interpretation of Phase 1 clinical pharmacology studies. They will serve as the primary lead on project teams, ensuring integration of pharmacology principles into development plans and regulatory submissions.
Director, Omnichannel Marketing
Crinetics Pharmaceuticals
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Full Time
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a month ago
Crinetics Pharmaceuticals
The Director of Omnichannel Marketing will design and execute integrated strategies to engage patients and healthcare professionals across various digital and non-personal channels. They will lead cross-functional teams to ensure consistent messaging, optimize channel mix, and drive measurable impact through data-driven insights.
The Contracts Manager will lead the drafting, review, and negotiation of various agreements including MSAs and SOWs to support Technical Operations and G&A functions. This role also involves managing high-volume contract workflows, ensuring GxP compliance, and providing training on contracting processes and tools.
Manager, Clinical Business Operations
Crinetics Pharmaceuticals
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Full Time
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a month ago
Crinetics Pharmaceuticals
The Manager, Clinical Business Operations will develop, negotiate, and execute site budgets for late-phase clinical trials while ensuring compliance with financial policies and regulations. They will also collaborate with cross-functional teams and CRO partners to track budget metrics and drive process improvements.
Director, Global Product Leader
Crinetics Pharmaceuticals
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Full Time
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2 months ago
Crinetics Pharmaceuticals
The Director, Global Product Leader will lead cross-functional global product teams to oversee strategic planning, budget management, and the successful progression of development programs. This role acts as the CEO's delegate to ensure alignment across discovery, regulatory, CMC, and commercial functions through to product launch.
Senior Clinical Research Associate
Crinetics Pharmaceuticals
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Full Time
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2 months ago
Crinetics Pharmaceuticals
The Senior Clinical Research Associate oversees clinical trial progress by conducting site visits and ensuring compliance with Good Clinical Practices and study protocols. They collaborate with the study team to manage site relationships, verify data integrity, and resolve performance or compliance issues.
Director, Quality Engineering
Crinetics Pharmaceuticals
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Full Time
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4 months ago
Crinetics Pharmaceuticals
The Director of Quality Engineering will lead the development and execution of global GMP quality engineering strategies and oversee the design and implementation of scalable, risk-based quality frameworks. This role includes strengthening inspection readiness and driving a robust CAPA culture across the organization.