Negotiate Clinical Trial Agreements with assigned sites to ensure alignment with Biogen’s interests.
Manage status tracking and reporting, keeping all stakeholders informed and updated.
Attend study team meetings to collaborate on study progress and contract execution.
Negotiate Master Clinical Trial Agreements as necessary to support study objectives.
Support CROs with contract negotiations and serve as an escalation point for unresolved issues.
Analyze contract trends to identify and implement process improvements.

Bachelor's Degree in a scientific or business discipline
JD/Paralegal Certification preferred
A minimum of 2 years’ experience in the biotechnology/pharmaceutical industry, specifically in site contract negotiation and execution across Phase I-IV clinical trials
Thorough understanding of GCP, relevant ICH standards, and FDA/EMA guidelines
Excellent negotiation, conflict resolution, and communication skills
Ability to manage time and priorities independently with minimal oversight.

Medical, Dental, Vision, & Life insurances
Fitness & Wellness programs including a fitness reimbursement
Short
and Long-Term Disability insurance
A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
Up to 12 company paid holidays + 3 paid days off for Personal Significance
80 hours of sick time per calendar year
Paid Maternity and Parental Leave benefit
401(k) program participation with company matched contributions
Employee stock purchase plan
Tuition reimbursement of up to $10,000 per calendar year
Employee Resource Groups participation

Site Contracts Analyst – Clinical Trial Site Contracts

Key skills