Job Description
📋 Description Manage preparation, negotiation, tracking, and execution of clinical trial site agreements and Negotiate with clinical research sites on budgets, payments, amendments, and confidentiality Prepare, review, process, and maintain contracts per policies and quality requirements. Coordinate with study teams, sponsors, and stakeholders on timelines and progress. Identify delays/risks and escalate to ensure timely resolution. Maintain organized contract files and ensure accessibility of executed agreements. 🎯 Requirements Bachelor’s degree preferred in law, business, life sciences, healthcare, or related field. 2–4 years of relevant experience in clinical research contracting or related operations. Experience with clinical study processes, site agreements, and contract negotiations. Understanding of clinical trial protocols, ICH GCP principles, and related regulations. Strong negotiation, communication, and organizational skills. Proficiency with Microsoft Office and contract/tracking systems. 🎁 Benefits Competitive annual salary USD 70,000–90,000, based on experience. Healthcare coverage (medical, dental, vision). Life insurance and disability coverage. 401(k) retirement plan. PTO or flexible time off options. Company bonus opportunities where applicable.