Job Description
Develop protocols, clinical study reports, investigators brochure, informed consent documents and other regulatory documents as per SOPs and applicable style guides.Handle at least 2 projects in a month.
Coordinate with data management, project management, medical monitoring and regulatory teams during development of project deliverables.
Coordinate with Sponsor from initialization to finalization of project deliverables.
Update senior medical writer of project status.
Keep pace with regulatory guidance and client expectations, and to improve skills.
Participate in the business development meetings.
Review regulatory documents prepared by the Junior Medical Writer and assist them in developing documents.
Provide relevant training to new employees.
Have a good knowledge of drug development process and regulatory guidelines.
Develop good working relationships with internal and external colleagues
Company Description
With over 1900 beds and 12 hospitals in Delhi-NCR, Punjab and Uttarakhand, over 1600 world-class doctors and 5400 support staff, Max Healthcare is one of the leading chain of hospitals in India. With 275 ICU beds & the most advanced technology, our state-of-the-art infrastructure is rated the be est in North India thereby making Max Healthcare one of the best hospitals in India
Additional Information
Minimum experience: Two years
- Education: M.Sc.
- APPLY
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