We are currently seeking a full time, office-based Clinical Research Project Coordinator Entry to join our Clinical Trial Management team in Navi Mumbai, India. This position will work on a team to accomplish tasks and projects that are instrumental to the company s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the prospect for you.
Responsibilities
Engage in clinical trial management on a day to day level;
Work closely with the project CTM for timely delivery of recurrent tasks consistently with a high degree of accuracy;
Compile and maintain project-specific status reports;
Update CTMS with study milestones, enrolment projections etc.
Update eTMF and perform ongoing eTMF QC;
Support clinical trial manager to draft study plans and study specific guidance documents;
Manager site feasibility, site activation preparation and study supply managements;
Communicate with regional cross functional team, vendors and sponsor effectively;
Qualifications
Bachelors degree in a life sciences field;
Maintain thorough knowledge of project and ability to coordinate/present at internal/external meetings and conference calls;
Excellent computer (word-processing, databases, Excel, Windows) and organizational skills.
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
📌 Clinical Project Coordinator Entry Mumbai (India)
🏢 Medpace Clinical Research India
📍 India
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