This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Project Specialist (Clinical Experience) based in India.

Join a collaborative clinical research workplace dedicated to advancing healthcare and accelerating the development of innovative treatments. In this role, you will coordinate clinical study activities, manage timelines, and support the successful delivery of clinical trials. You will work closely with cross-functional teams, including clinical operations, regulatory affairs, and data management, to ensure project milestones are achieved efficiently. Your expertise will contribute to maintaining regulatory compliance, optimizing study budgets, and resolving operational challenges. You will also help standardize processes, monitor study performance, and develop effective patient recruitment strategies. This opportunity is ideal for an organized, detail-oriented professional who thrives in a dynamic environment and wants to make a meaningful contribution to clinical research and patient outcomes.
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Accountabilities

• Clinical Project Planning: Develop, coordinate, and communicate clinical study timelines, ensuring key milestones and deliverables are achieved according to project objectives.

• Cross-Functional Coordination: Gather input from clinical, regulatory, data management, and other relevant teams to develop comprehensive project plans and facilitate timely execution.

• Study Operations and Compliance: Oversee clinical trial activities, resolve operational challenges, and ensure compliance with standard operating procedures (SOPs), Good Clinical Practice (GCP), and applicable country-specific regulations.

• Process Improvement: Promote consistency across clinical studies by standardizing procedures, implementing best practices, and supporting continuous operational improvement.

• Site and Vendor Management: Support the selection of clinical research sites and vendors,

📌 Project Specialist (India)
🏢 Jobgether
📍 India