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Job Description
Structured overview of role & requirementsAbout This Role
Lead cross-functional teams to plan, execute, and close global electronic Clinical Outcome Assessment (eCOA) studies ensuring timelines, budgets, and quality targets are met.
Manage study documentation, financials (budget, forecast, invoices), and device logistics throughout the project lifecycle.
Serve as primary liaison for stakeholders (sponsors, vendors, internal teams) to drive project success, risk mitigation, and effective communication.
Minimum Requirements
Bachelor's degree or equivalent combination of education and relevant project management experience.
1 to 4 years of project management experience in pharmaceutical, biotech, healthcare, clinical research, life sciences, or related industries.
Experience in managing projects involving technology-enabled clinical trials, especially eCOA, ePRO, eConsent, or RTSM/IRT is preferred but not strictly mandatory.
PMP certification is preferred but not explicitly mandatory; strong financial management skills and English communication proficiency required.
Ideal Candidate Profile
Experienced in clinical trial environment with understanding of drug development processes and eClinical solutions.
Operating style involves managing multiple stakeholders, timelines, and budgets with strong risk management and problem-solving abilities.
Comfortable working India-based with global teams including U.S. time zone collaboration; capable of supporting operational readiness and training activities.
