Senior Medical Writer, Evidence Analyst
Posted 19hrs ago
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Job Description
Senior Medical Writer authoring and reviewing regulatory medical writing deliverables for clinical studies. Supporting other writers and undertaking quality control across various domains while adhering to ICH regulations.
Responsibilities:
- Author, review regulatory & other medical writing deliverables independently or with other Sr Medical Writer
- Support other writers for manuscripts, slide sets, abstracts, posters, other techno-commercial documents as needed
- Authoring & review of patient narratives, CSRs, Protocol, IB, & other regulatory submission documents
- Independent authoring and review of manuscripts, abstracts, posters, evidence synthesis projects and other techno-commercial documents
- Undertake quality control of the aforementioned deliverables
- Showcase flexibility in terms of timelines and writing style based on client needs and therapeutic area requirements across various domains.
Requirements:
- PharmD, M. Pharm, PhD, MD, Post-graduate degree in Life science/medical/para medical
- At least 3-5 years of experience in medical writing or flair for writing with proven academic standards
- Fair understanding of industry standards and global trends in drug development and medical device domains
- Highly proficient in MS Office and other software for authoring and data handling/interpretation
- Basic understanding and comfort for use of automation platforms
Benefits:
- Commitment to excellence and high standards
- Creative, flexible, and innovative team player
- Good judgement with the ability to make timely and sound decisions










