Generate Biomedicines
Counsel, Clinical Contracting
$150K–$188K
Somerville, MA +1 · Full-time · Posted Oct 30, 2026
- Location
- Somerville, MA
Somerville, Massachusetts, United States - Experience
- 5+ years of relevant clinical contracting experience.
- Education
- JD from an accredited law school; admitted to practice in at least one US jurisdiction.
About the job
Manage and negotiate global clinical site agreements and related documents to support late-phase clinical studies.
What you'll do
- Review, draft, negotiate, and finalize clinical research agreements and supporting documents using approved templates and fallback positions.
- Coordinate with internal stakeholders, CROs, and clinical sites; track document flow and address contracting bottlenecks.
- Flag contract risks and deviations, escalate complex issues, and suggest improvements to templates and workflows.
What they ask for
- 5+ years of clinical contracting experience in a biotechnology, pharmaceutical, or CRO environment.
- Deep working knowledge of clinical site contracts and regulatory support documents, with experience negotiating directly with clinical sites, academic institutions, and/or investigators.
- Ability to independently redline and finalize contracts and manage high-volume workflows under tight timelines.
- JD from an accredited law school and admission to practice in at least one US jurisdiction.
Nice to have
- Experience with both US and international clinical site contracting.
- Familiarity with ICH-GCP, HIPAA, GDPR, or contract lifecycle management (CLM) systems.
Pay
$150,000 — $188,000 USD per year (base salary)
Tools
ICH-GCP, HIPAA, GDPR, CLM
Model-written summary · the original posting is authoritative