Hyderabad;Regional Clinical Reseach Associate; M.Pharm; Vimta Labs

Company Name
Vimta Labs
Job Description

 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
 Regulatory templates
 Prepare/Process
 (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%

Location
Mumbai, Noida
Experience
1 - 3 years
Education
MBBS, MD/MS, M.Pharm, M.Sc, PG Diploma

send resumes to: careers@vimta.com or recruitment@vimta.com