Site Contracts Associate II

About the Role:

• This role sits at the core of clinical trial execution, ensuring site agreements are accurately drafted, negotiated, and executed.
• You will work closely with clinical sites, internal study teams, and cross-functional stakeholders to manage contract lifecycles.
• The position requires strong attention to detail, legal and contractual interpretation skills, and balancing compliance with operational timelines.

Key Accountabilities:

• Draft, review, and negotiate clinical site agreements, service agreements, amendments, and related documents.
• Manage the full contract execution process, including coordinating signatures and tracking milestones.
• Identify risks and issues in contract terms and collaborate with stakeholders to resolve them effectively.

Requirements:

• 2–5 years of experience in site contracting, clinical operations, or a related role within the CRO or life sciences industry.
• Bachelor’s degree in law, business, economics, or social sciences, or equivalent professional experience.
• Strong understanding of clinical trial processes, site agreements, and regulatory requirements such as ICH-GCP.

Benefits:

• Opportunity to contribute directly to global clinical trials that support development of life-changing therapies.
• Fully remote working model based in India with exposure to international stakeholders.
• Structured learning and development opportunities within the clinical research industry.