Incorporated in 1996, SIRO Clinpharm Private Limited is a Clinical Research Organisation supporting trials from Phase II to Phase IV and beyond post-launch of products. SIRO offers a range of services, from clinical operations to data services, data analytics and medical writing in compliance with international standards. SIRO has been an industry pioneer over two decades, sharing an incontestable record of excellence in the pharmaceutical, FMCG and medical device industry. Its global delivery centre in Thane has a seasoned team of more than 200 professionals hailing from science and medical backgrounds.
Post : Senior Regulatory Medical Writer
No of Vacancies : 8 to 10
Work Location : Hybrid / Remote Working
Job Description : Draft and review of regulatory medical writing documents (CSRs, Protocols, ICDs, IBs, Table of Studies, CSR Narratives, Clinical Overviews, Clinical Summaries, briefing books, etc) in accordance with applicable guidelines and SOPs
Candidate Profile : Qualified doctor (MD/ MS or MBBS/ BAMS/ BHMS/ BDS) and/ or PhD and / or Graduate or post graduate in Pharmacy or life sciences Experience : 5 to 7 years, Experience in authoring and reviewing of clinical trial (Phase 2 to 4) documents is mandatory (BA/BE experience is not considered)
Share profiles on veda.dhamankar@siroclinpharm.com
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