Ready to explore a new career development opportunity?
At Covance, you can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world.
Our commitment to this mission has resulted in Covance’s impressive history of company stability and growth. We’ve achieved these results by fostering a work environment that encourages, develops and leverages our team’s capabilities.
Covance’s ongoing success offers team members unsurpassed growth and career development opportunities. There’s no better time to join us!
As a Lead Medical Writer you will experience working on cutting edge global clinical trials and have responsibilities that cover:
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
Ensure compliance of operations with governing regulatory requirements
Create, maintain and assume accountability for a culture of high customer service
Efficiency in conducting literature searches for authoring various types of reports
Write various safety reports (or part of such reports) for global regulatory submissions for Sciformix’s clients, including Annual Reports (IND and other), Periodic Safety Update Reports, Periodic Adverse Drug Experience Reports, Bridging reports and other clinical documents as assigned.
Write Common Technical Document Summaries including Non Clinical and Clinical Overviews, Clinical Summaries and other regulatory documents as assigned.
Write Investigator Brochures and sections of/entire protocols
So if you are looking to join a company that will help grow your career and provide opportunities to develop your skills in a global company why not apply today?
Bachelors - Any Life Sciences
- Ideally 6+ years of experience in Medical writing
- Post Marketing and PV experience preferred
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