Sr Clinical Research Associate - Vimta Labs Ltd

Qualification – M Pharm/ MSC/ Pharm D/ B Pharm

Experience – 4-8 years 

• Act as site monitor for a clinical trial (patients trial) projects of various therapeutic areas
• Performing Quality Check of Regulatory Documents & Trial Master Files
• Contribute to creating Local Working Procedures/SOP and associated system documents.
• Extensive knowledge in ICH GCP guideline and New Drugs Clinical Trial Rules 2019
• Responsible for the preparation of CTA, MOU or any other relevant contracts with the vendors and customers as per the need of the study
• Performing trial feasibilities and site identification and Site Selection Visits
• Willing to travel both locally and to the outstation at least 10 to 15 days a month.
• Preparation of organization/department for the purpose of Audit (Internal Audit, regulatory or Sponsor or any other form of Audit)
• Responsible for performing Study initiation and monitoring visits and close out visit according to study monitoring plan.

Interested candidates can share their resumes to keerthana.rojanala@vimta.com