Senior CTM

• 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.

• 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.

Medical, dental, vision, 401(k), telehealth services, ESOP, and commuter benefits.