Associate Clinical Project Manager
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Job Description
Associate Clinical Project Manager at Crinetics Pharmaceuticals supporting clinical project management and collaborating with cross-functional teams on studies. Managing budgets and timelines effectively.
Responsibilities:
- Provide routine and daily support to clinical project management team
- Collaborate closely with clinical project management and cross-functional teams to establish priorities
- Assist with development, maintenance, and management of high-quality detailed study timelines as assigned
- Under oversight of CPM, may be assigned management of study(ies)
- Support or management of routine status reporting, including study timeline and budget dashboards and management updates
- Contribute to development of study budget and maintenance of monthly study budget forecasting and routine budget review in partnership with CTO and finance
- Support cost accruals by study managers to ensure accurate reporting to finance and consistent approaches across all Crinetics-sponsored clinical trials
- Collaborate with CPMs and study managers to collect and analyze forecasted and accrued costs to produce at-a-glance data displays summarizing project financial health
- Collate and maintain current budget value by study based upon fully executed agreements
- Routinely update and maintain an accurate listing of all current and planned studies
- Support maintenance and timely updates to key tasks and milestones across studies to support Project and Portfolio Management for entry into corporate project management system.
- Share lessons learned and best practices across programs
- Provide feedback and assist with the development of departmental procedures toward increased efficiency and quality of deliverables.
- Contribute to the development of procedural documents.
- Facilitate or oversee clinical project management team processes
- Provide back-up support for CPMs as needed
Requirements:
- Bachelor’s in related discipline required; a combination of relevant education and applicable job experience may be considered.
- 5 years of related experience in a CRO, Biotech or Pharmaceutical organization is required.
- Solid understanding of drug development and clinical operations.
- Excellent organizational and time management skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively.
- Excellent computer skills including advanced knowledge in MS Excel, Word, PowerPoint and Outlook.
- Must be a self-starter who works with minimal supervision.
- Works effectively in a matrix cross-functional environment.
- Good business judgment and a strong understanding of the unique aspects of clinical financials.
- Excellent communication skills, (verbal and written) including the ability to understand and present budget information effectively.
Benefits:
- Health insurance plans including medical, dental, vision and basic life insurance
- 20 days of PTO
- 10 paid holidays
- Winter company shutdown
- Discretionary annual target bonus
- Stock options
- 401k match
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