The role involves developing and tracking project plans, managing timelines, budgets, and deliverables, and collaborating closely with clinical, regulatory, logistics, and vendor teams to resolve issues and mitigate risks. The individual will prepare project documentation, status reports, and metrics, support compliance with global regulations and internal standards, and contribute to continuous improvement of operational methodologies. Day-to-day responsibilities also include stakeholder communication, escalation management, and proactive identification of process enhancements to keep studies on schedule and within scope.
Qualifications
Candidates should possess strong Project Management and Project Planning skills to manage clinical trial supply chain projects, timelines, and deliverables.




Candidates should possess solid Program Management capabilities to coordinate multiple studies or workstreams and align cross-functional efforts.
Candidates should possess excellent Analytical Skills to interpret data, assess risks, optimize supply strategies, and support decision-making.
Candidates should possess clear and professional Communication skills to collaborate with internal teams, external partners, and trial sites.
Experience in clinical research, clinical operations, or clinical supply chain management, preferably within biopharmaceutical or medical device sectors.
Strong organizational skills, attention to detail, and the ability to manage multiple projects in a fast-paced, regulated setting.

📌 Project Management (India)
🏢 Intrinseque Health
📍 India