Require Project Coordinator at Medpace

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Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing approximately 3,500 people across almost 40 countries.

Post : Project Coordinator - Core Labs

Job Description

  • Responsible for all day-to-day Project Coordination activities;
  • Compile and maintain project-specific status report;
  • Utilize and assist in maintaining ClinTrak Imaging ® system;
  • Independently interact with Sponsor, sites, other contractors, and Medpace Core Laboratories team;
  • Prepare and review presentation materials;
  • Create and maintain project timelines in Microsoft Project;
  • Work with Project Manager to ensure all necessary project documents are present;
  • Maintain supplies inventory for study sites and organize shipping efforts of study materials;
  • Copy and distribute study documentation/correspondence to Sponsor, site, and Medpace Core Laboratories project team and assist in the review and resolution of site queries;
  • Schedule project meetings (internal and external), be active participant and provide post-meeting documentation/minutes; and
  • Provide insightful input on project-related documents (essential document collection process, final analysis plan, final study report, etc.).

Candidate Profile
• Bachelor of life science, biotechnology, or pharmacy, and 3-year project coordinator experience or equivalent; or, Master of life science, biotechnology, pharmacy, and 1-year project coordinator experience or equivalent;
• Comprehensive knowledge of Good Clinical Practice Guidelines and Sponsor Standard Operating Procedures (SOPs);
• Experience with clinical trials for device or pharmaceutical products;
• Ability to interact with other departments and Sponsors on project-related issues;
• Independent development and management of project-related documents (i.e., status reports, essential documents, timelines, etc.);
• Proficient knowledge of Microsoft Project, Microsoft Office Products (Word, Power Point, Excel, etc.);
• Must be fluent in English (Verbal and Written); and
• Excellent attention to detail, strong multi-tasking skills, and flexibility with changing priorities.

Additional Information
Qualification :
B.Sc, B. Pharm
Location : Navi Mumbai
Industry Type : Pharma / Healthcare / Clinical research
Functional Area :Core Labs
End Date : 30th November, 2020

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