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A South San Francisco based pharmaceutical company is looking for a Contract Senior CTM to join their growing clinical team.
Job Responsibility:
Lead global cross-functional study teams through all study stages
Provide support and contribute to RFP/RFI process, analyze service providers, budgets/proposals, conduct bid defense meetings, award services, negotiate and execute complex agreements (i.e., CRO, study related collaboration agreements)
Manage CRO and service providers
Assist with Inspection Readiness activities
Manage clinical study timelines with PM Team
Develop study documents such as CRF design, project plans, Service Provider Oversight plans
Manages study sites and study related activities (site selection, start up, recruitment, enrollment, study management, monitoring report review, and more)
Provide regular updates to Study lead and other stakeholders
Proactively identify, manage, or escalate issues appropriately
Work with Finance to manage budget for studies and vendors
30% of travel.
Requirements:
Minimum Bachelor’s degree in a relevant scientific discipline
Minimum 7 years of pharma or biotech industry experience managing clinical trials
Sponsor experience required
Global Study Management experience in Phase III required
CRO & Vendor Management experience required
Metabolic, Cardiovascular, or Diabetes experience required
Proven experience driving enrollment and retention strategies for large, complex patient populations in global clinical trials.
What we offer:
Medical, dental, vision, 401(k), telehealth services, ESOP, and commuter benefits.