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Associate Director – Clinical Project Management
Crinetics PharmaceuticalsAssociate Director overseeing Clinical Project Management activities for multiple studies at a clinical-stage pharmaceutical company. Responsible for timeline, risk, and budget management in clinical trials.
About the role
Key responsibilities & impact- Oversee timeline, budget and accruals for the clinical studies and clinical programs within the Clinical Operations group
- Develop, maintain, and manage high-quality consistent study processes and templates with cross-functional Clinical Operations peers to drive consistent and reliable clinical study outcomes
- In collaboration with the Project and Portfolio Management, provide clinical program timeline and budget estimates to support annual budgets and long-range planning (LRP)
- Oversee and mentor team of Clinical Project Managers as needed
- Develop and oversee policies and procedures aimed to streamline Clinical Project Management process
- In collaboration with Clinical Trial Operations and Project and Portfolio Management, provide input on annual planning activities to meet corporate study and program objectives
- Subject Matter Expert (SME) for study and program clinical timelines and budgets
- Oversee routine status reporting including study timeline and budget dashboards and management updates
- Ensure teams are providing monthly milestone and timeline updates to Project and Portfolio Management for entry into corporate project management system
- In collaboration with Project and Portfolio Management, develop program scenario plans and support life cycle management activities as needed, support creation and incorporation of resource demand algorithms into project management software
- Oversee and streamline monthly accrual process in partnership with finance
- Facilitate and oversee cost accruals by study managers to ensure accuracy
- Meet with finance periodically to review accrued costs against forecasts and troubleshoot variances, and to oversee overall spend for studies & programs
- Identify potential budget issues and recommend and implement solutions or corrective actions as needed
- Provide program-level timeline and financial health summaries for management periodically
- Other duties as assigned
Requirements
What you’ll need- Bachelor’s degree in a related discipline required; a combination of relevant education and applicable job experience may be considered
- Minimum of 10 years of progressive experience in clinical project management within a CRO, biotechnology, or pharmaceutical organization, including people leadership responsibilities 7 years of supervisory experience
- Strong understanding of drug development, clinical operations, and clinical financial management
- Demonstrated leadership capability with experience mentoring and overseeing project management staff
- Excellent organizational, time management, and communication skills, with the ability to manage multiple priorities in a matrix environment
Benefits
Comp & perks- discretionary annual target bonus
- stock options
- ESPP
- 401k match
- top-notch health insurance plans for employees (and their families) to include medical, dental, vision and basic life insurance
- 20 days of PTO
- 10 paid holidays
- winter company shutdown
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical project managementbudget managementtimeline managementresource demand algorithmsaccrual processstatus reportingfinancial health summariespolicies and procedures developmentproject management software
Soft Skills
leadershipmentoringorganizational skillstime managementcommunication skills