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Medpace Hiring e-Clinical Coordinator in Clinical Research

Published on

Medpace

1 to 2 Years

Not disclosed

mumbai

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences

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Medpace, a full-service clinical contract research organization (CRO), is looking for a full-time eClinical Coordinator to join their Data Management/eClinical team in Mumbai. The role involves supporting the eClinical Project Manager and ensuring accurate patient-reported data for clinical studies. If you have strong attention to detail, enjoy working in a structured environment, and are seeking a predictable work environment, this could be a great opportunity for you.

Key Responsibilities:

  • Assist the Project Manager in system design and setup for clinical studies.
  • Create study-specific documents.
  • Track and provide key study metrics and project monitoring.
  • Communicate with clients to obtain requirements and respond to inquiries.
  • Handle other assigned projects and tasks as needed.

Qualifications:

  • Bachelor’s degree in a health-related field.
  • Strong attention to detail with proficiency in Excel and Word.
  • Knowledge of medical terminology.
  • 1-2 years of experience in a pharmaceutical or CRO setting preferred.
  • Travel: None required.

About Medpace:

Medpace is a leading clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 people across 40+ countries and has been recognized for its impact on patient lives across numerous therapeutic areas.

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