Senior Analyst, Site Contracts - Remote

Overview

The Sr Analyst, Site Contracts is responsible for the preparation of clinical trial agreements, master clinical trial agreements, related ancillary services agreements and amendment templates as well as the negotiation of language, budgets, and payment terms with clinical sites and ancillary facilities.

In Short

• Prepare appropriate contract templates to streamline negotiations.
• Work with study and legal teams to meet startup timelines and protect company interests.
• Manage tracking and reporting from draft to execution ensuring audit readiness.
• Serve as an escalation point for language issues from external entities.
• Analyze contract trends and support process improvements.
• Mentor site contracts analysts.
• Ensure contracts are amended in a timely manner throughout study lifecycle.
• Collaborate effectively in cross-functional teams.
• Resolve issues in a collaborative environment.
• Accomplish challenging goals in the biotechnology/pharmaceutical industry.

Requirements

• Bachelor’s Degree required, JD/Paralegal Certification preferred.
• 4+ years’ experience in site contract and budget negotiation.
• Experience in clinical research processes and understanding of GCP.
• Knowledge of industry fair market value and legal terms.
• Excellent negotiation and communication skills required.
• Ability to manage time and priorities with minimal oversight.
• Ability to work effectively in cross-functional teams.

Benefits

• Medical, Dental, Vision, & Life insurances.
• Fitness & Wellness programs.
• Short- and Long-Term Disability insurance.
• 15 days of paid vacation plus additional shutdown time.
• 12 company paid holidays and 3 days for Personal Significance.
• 80 hours of sick time per year.
• Paid Maternity and Parental Leave.
• 401(k) with company matched contributions.
• Employee stock purchase plan.
• Tuition reimbursement up to $10,000 per year.