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Clinical Project Coordinator Jobs in Medpace

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B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences or relevant Feild

Navi Mumbai

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Medpace is hiring for a Clinical Research Project Coordinator position in Navi Mumbai, India. The full-time, office-based role is part of the Clinical Trial Management team and involves supporting clinical trial management activities, maintaining study documentation and systems, coordinating project tasks, and working with cross-functional teams, vendors, and sponsors.

Job Details

Job DetailsInformation
CompanyMedpace
PositionClinical Research Project Coordinator
Job LevelEntry
Job CategoryClinical Trial Management
LocationNavi Mumbai, India
Job TypeFull-time, office-based
Job ID12947

Position: Clinical Research Project Coordinator

The Clinical Research Project Coordinator will work closely with the Clinical Trial Manager (CTM) to support day-to-day clinical trial management activities and ensure timely and accurate completion of recurring project tasks.

Responsibilities

  • Support day-to-day clinical trial management activities.
  • Work closely with the project CTM to deliver recurring tasks accurately and on time.
  • Compile and maintain project-specific status reports.
  • Update CTMS with study milestones and enrollment projections.
  • Update eTMF and perform ongoing eTMF quality control.
  • Support the Clinical Trial Manager in drafting study plans and study-specific guidance documents.
  • Manage site feasibility and site activation preparation.
  • Support study supply management.
  • Communicate effectively with regional cross-functional teams, vendors, and sponsors.

Eligibility & Qualifications

  • Bachelor’s degree in a Life Sciences field.
  • Thorough knowledge of projects.
  • Ability to coordinate and present at internal and external meetings and conference calls.
  • Excellent computer skills, including:
    • Word processing
    • Databases
    • Excel
    • Windows
  • Strong organizational skills.

Required Skills

  • Clinical trial management
  • Project coordination
  • CTMS
  • eTMF management and QC
  • Clinical study documentation
  • Site feasibility and activation
  • Study supply management
  • Cross-functional communication
  • Vendor and sponsor communication
  • Microsoft Excel and other computer applications
  • Organization and presentation skills

Application Details

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APPLICATION DETAILS

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