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Clinical Research Associate/Co-ordinator - India  

Navitas Life Sciences (company)

Posted on : 22 December 2017

Project Description

Category: Executive
Location: Manipal and Mangalore
Job Type:
Full Time
Education: B.Pharma or M.Pharma or M.Sc (Pharmacology)

Job Description:

  • Registration of Volunteers
  • Preparation, revision and updating of Standard Operating Procedures. Imparting training to staff on relevant SOPs
  • Assisting the Principal Investigator in Review of Study Documents like Protocol and Clinical Study Reports
  • Serving as Sub-investigator/ Research associate in the assigned clinical studies
  • Submission of Protocol and its appendices, and other documents as mandated, to IEC for approval
  • Counseling of the volunteers, answering their queries and seeking informed consent from them prior to screening and clinical studies
  • Co-coordinating the screening-related activities
  • Collection, recording of clinical data, verification, compilation and maintenance of Case Record Forms
  • Collection of necessary documents for, compilation, filing and maintenance of Screening Files, Study Specific Files and Study Master File / investigator Site File
  • Documentation of the conduct of various screening and study-related procedures in the respective log books
  • Preparation of study updates and providing data for generation of Clinical Study Report
  • Close-looping of QA observations on the assigned studies

Preferred Skills:

  • Preferably 1to 4 years of experience in Clinical-BA/BE

If you would like to apply for this position, or would like a discussion about this, or any other role, please send your contact details, together with your curriculum vitae to: