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Job Location | Hyderabad |
Education | Not Mentioned |
Salary | Not Disclosed |
Industry | Pharma / Biotech |
Functional Area | Medical Transcription |
EmploymentType | Full-time |
Medical Writer Biopeople India Job details Job Details Medical Writer Description : Develop protocols, informed consent documents, clinical study report, investigator brochure and other regulatory documents Coordinate with Sponsor from initialization to finalization of project deliverables Handle at least 2 projects in a month Update the management and team members of project status and participate in team meetings Participate in business development meetings Provide relevant training to other team members Develop good working relationships with internal and external colleagues CTC : 7- 10 Lac/ Annum,
Keyskills :
clinicaltrials informedconsent businessdevelopment clinicalstudy edicalWriter