Job as Regional CRA
Vimta Labs is India’s leading contract research and testing organization. Established in 1984 VIMTA has an envious track record of serving several market leaders across the globe.
VIMTA is a team of 707 professionals comprising 442 scientists in various disciplines such as Chemistry, Pharma, Medicine, Microbiology, Molecular biology and Informatics. The team is slated to double in next three years.
VIMTA is a multi-site organization with more than 300,000 sqft world class laboratory facilities.
The technologies deployed at VIMTA are current and leading edge, duly validated.
-Manage clinical trial sites by performing routine monitoring visits to ensure
-The trial is carried out in accordance with the GCP guidelines, company SOPs and currently approve protocol amendment( s )
-Progress of the project
-Enrollment targets are met
-The rights and well-being of human subjects are protected
-Reported trial data are accurate, complete and verifiable from source documents
-Recruit Investigators and negotiate budgets for participation in clinical trials
-Review/Obtain Draft protocols for completeness and feasibility
-Regulatory and administrative documents from the trial sites for completeness
-Conduct of the clinical trial
-Case Report Forms
-Source document template
-(Serious) adverse event report
-Project status reports for management
-Clinical study reports at the end of the study
-Presentations at Investigator meeting
-Participate in company required training programs
-Required overnight travel is approximately 40%
-Candidate should be M.Pharm, M.Sc, MBBS, B.D.S, P.G. Diploma or Degree in Clinical Research and shold have 1-3 years of releavent experience.
Experience: 1-3 years
Education: M.Pharm, M.Sc, MBBS, B.D.S, P.G. Diploma or Degree in Clinical Research, MD/MS
Functional Area: Pharmaceutical/ Biotechnology
Industry Type: Pharma/ Biotech/Clinical Research
Reference: REG CRA