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Vaf 175 Medical Writing Specialist

Productlife Group
ProductLife Group
2+ years
Not Disclosed
10 April 30, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

VAF 175 Medical Writing Specialist
Location: India (Remote work possible)
Job Type: Permanent contract
Department: Life Cycle - Regulatory Affairs & Operations


Responsibilities

  • Conduct comprehensive toxicology risk assessments across diverse scenarios, ensuring robust safety evaluations.

  • Review and conduct toxicology risk assessments for excipients, impurities, solvents, extractables, and leachables, ensuring adherence to regulatory standards.

  • Execute Environmental Risk Assessments (ERA) in compliance with the latest EMA guidelines.

  • Prepare, maintain, and update toxicology summaries for globally marketed products in alignment with company policies.

  • Develop and compile PDE and OEL monographs to support safety evaluations.

  • Prepare clinical and non-clinical dossier modules (Modules 2.4, 2.5, 2.6, 2.7, 4, and 5) for regulatory submissions.

  • Manage preclinical studies and associated documentation to ensure compliance and accuracy.

  • Perform QSAR genotoxicity assessments in accordance with ICH M7 guidelines.

  • Utilize advanced in-silico predictions (DEREK, SARAH, NEXUS, TOXTREE, OECD Toolbox) for data analysis and risk assessment.

  • Provide expert guidance in addressing client and regulatory inquiries effectively.


Background Required

  • Qualified Toxicologist with experience in signing non-clinical/toxicological reports, modules, and expert reports.

  • Experience in drafting Environmental Risk Assessment (ERA) reports.

  • Proficient in due diligence of pre-clinical data and drafting strategy for non-clinical studies for complex generics, NCEs, Biologics, etc.

  • Experience in drafting and reviewing non-clinical CTD modules.

  • Experience in drafting PDE reports and toxicological risk assessments for impurities, leachables, and extractables.


Required Education

  • Qualified and experienced Toxicologist.


Required Experience

  • At least 2 years of experience in the above-mentioned activities.