Job Description
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 Labcorp’s 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 reactions and adverse events they process
• Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, ****** orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
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 Labcorp’s 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 reactions and adverse events they process
• Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, ****** orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
💡 Quick Summary
Seeking a career-building opportunity? The Medical Writer Asst position is now open for candidates interested in the Content Writer Jobs sector. This role in Pune offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Content Writer Jobs is a plus.
