Medical Writer Asst
Published date: 2026/11/07
- Location: Pune, Maharashtra, India
1) Implement and promote use of consistent, efficient and quality processes to meet timelines and deliverables according to requirements and standard operating
procedures, and assume accountability for the deliverables
2) Ensure compliance of operations with governing regulatory requirements
Create, maintain and assume accountability for a culture of high customer service
Perform literature searches (clinical and non-clinical) and write non-clinical and clinical submission documents
3) Write parts of various safety reports for global regulatory submissions for Labcorpâs clients, including Annual Reports (IND and other), Periodic Safety
Update Reports, Periodic Adverse Drug Experience Reports, Bridging reports
Assist in writing Investigator brochures and sections of protocols
4) Assist in writing Clinical Study Reports for Ph 1-4 trials, including full study reports, abbreviated reports, web synopses
5) Assist pharmacovigilance teams in writing narratives for the adverse drug...
procedures, and assume accountability for the deliverables
2) Ensure compliance of operations with governing regulatory requirements
Create, maintain and assume accountability for a culture of high customer service
Perform literature searches (clinical and non-clinical) and write non-clinical and clinical submission documents
3) Write parts of various safety reports for global regulatory submissions for Labcorpâs clients, including Annual Reports (IND and other), Periodic Safety
Update Reports, Periodic Adverse Drug Experience Reports, Bridging reports
Assist in writing Investigator brochures and sections of protocols
4) Assist in writing Clinical Study Reports for Ph 1-4 trials, including full study reports, abbreviated reports, web synopses
5) Assist pharmacovigilance teams in writing narratives for the adverse drug...
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