Skills
Clinical trial contract drafting
Contract lifecycle management (CLM)
Life sciences agreement review
About the Role
We are looking for a Life Sciences Paralegal to support legal teams serving pharmaceutical, biotechnology, medical device, and Contract Research Organization (CRO) clients. This is an existing opening and offers an opportunity to help manage the contract workflow that enables clinical research.
Responsibilities
- Draft, review, negotiate, and manage life sciences agreements, including Clinical Trial Agreements (CTAs), Clinical Site Agreements (CSAs), investigator agreements, and confidentiality agreements (NDAs/CDAs)
- Assist with contract negotiations involving clinical sites, hospitals, investigators, CROs, vendors, and strategic partners
- Support review and negotiation of clinical trial budgets in collaboration with Clinical Operations, Finance, and external sites
- Coordinate contract execution and maintain organized records using contract lifecycle management (CLM) systems or other repositories
- Partner with Legal, Clinical Operations, Procurement, Regulatory Affairs, Finance, and business stakeholders to keep agreements on track
Requirements
- Experience supporting pharmaceutical, biotechnology, medical device, and/or CRO clients
- Knowledge of clinical trial contract documents (e.g., CTAs and CSAs)
- Strong contract review and organization skills, including familiarity with CLM or similar tools
- Ability to work effectively across cross-functional teams and support negotiations
Benefits
- Opportunity to contribute to high-impact life sciences work across multiple stakeholders
- Supportive team environment focused on contract execution and operational readiness
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