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Principal Regulatory Medical Writing

Siro Clinpharm
Siro Clinpharm
7+ years
Not Disclosed
10 Sept. 11, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

We're thrilled to share that Siro Clinpharm is looking for a Principal Regulatory Medical Writer to join our Scientific Writing & Communications Team!

If you have over 7 years of experience in authoring and managing regulatory documents such as Clinical Study Reports (CSRs), Protocols, and Investigator Brochures (IBs), we want to hear from you.

Location: Remote/Hybrid - Mumbai

To apply, please send your resume to veda.dhamankar@siroclinpharm.com.