The role involves planning, coordinating, and monitoring clinical supply chain activities to support global clinical trials, ensuring that study materials, devices, and equipment are delivered, installed, calibrated, and maintained according to protocol and regulatory requirements. The professional in this role will collaborate with cross-functional teams, vendors, and clinical sites to manage timelines, risks, and budgets, while maintaining detailed project documentation and status reports. Day-to-day responsibilities include developing project plans, tracking milestones, resolving logistical and operational issues, and supporting process improvements to enhance efficiency and quality in clinical research operations.

The role also requires regular communication with clients and internal stakeholders to align project objectives, expectations, and deliverables.

Qualifications





- Candidates should possess robust Project Management and Program Management skills to oversee complex, multi-stakeholder clinical initiatives.
- Candidates should possess solid Project Planning and organizational skills to manage timelines, resources, and deliverables effectively.
- Candidates should possess robust Analytical Skills to interpret data, identify risks, and support evidence-based decision-making.
- Candidates should possess excellent Communication skills to collaborate with internal teams, external partners, and clients across regions.
- Experience in clinical research, clinical operations, or clinical supply chain management is highly beneficial.
- Familiarity with global regulatory and quality standards related to clinical trials and medical products is an advantage.

📌 Project Management - Clinical Research (New Delhi)
🏢 Intrinseque Health
📍 New Delhi