Manager, Site Contracts

Job Description:

• developing accurate and timely total investigator grants and per subject cost estimates
• reviewing CROs’ and/or sites’ proposed changes to the study-specific budget parameters
• ensuring the delivery of high quality, compliant, effective, and timely deliverables
• maintaining productive relationships with internal client groups
• leading ongoing process improvements and training sessions
• onboarding, training, and mentoring peers
• potentially having direct reports

Requirements:

• a minimum of a Bachelor’s degree required
• at least 5 years of relevant experience with clinical site contracting at a biopharmaceutical company or CRO
• Advanced degrees like a J.D. (Juris Doctorate) is highly preferred.

Benefits:

• health and wellness programs (including medical, dental, vision, life, and disability insurance)
• fitness centers
• 401(k) company match
• family support benefits
• equity awards
• annual bonuses
• paid time off
• paid leaves (e.g., military and parental leave) for eligible employees at all levels!