MakroCare is expert strategic development and commercialization global partner for pharmaceutical, biotechnology and medical device industries. Our experience, programs and processes bring a new dimension to development strategy, regulatory/risk planning & management, clinical research, medical/scientific support and emerging region expansion.
Post : Medical Writer
No of Posts : 03
Job Description
• Writing and reviewing clinical/regulatory documents such as clinical trial protocols, clinical study reports, investigator brochures, informed consent forms, and according to ICH or other guidelines
• Other writing jobs and responsibilities assigned time to time
• Develop templates for reports and other regulatory documents.
• Take initiatives in process improvement areas
• Lead and mentor other writers
• Ability to work across teams as well as independently
• Good communication & coordination with various people involved in the process
• Good time management, and meeting deadlines and commitments
Additional Information
Experience : 5-8yrs
Location : Hitech City, Hyderabad
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Medical Writer
Job Type : Permanent
End Date : 11/10/2019
Contact Person : Rajesh Neelam
Contact Email : rajesh.neelam@makrogrp.com
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