Scope and responsibilities • Author, review, and coordinate medical writing deliverables across the product lifecycle, from clinical development through the post-marketing phase. • Prepare and coordinate key clinical and regulatory documents, including clinical trial protocols, protocol amendments, clinical study reports, investigator’s brochures, submission documents, and responses to health authority questions. • Author and coordinate pharmacovigilance and safety-related documents, such as aggregate safety reports, risk management documentation, safety sections of regulatory submissions, signal evaluation reports, and other post-marketing safety deliverables. • Work cross-functionally with Clinical Development, Biostatistics, Pharmacovigilance, Regulatory Affairs, and other stakeholders to interpret and clearly present clinical and safety data. • Manage document plans, timelines, review cycles, and stakeholder input to ensure accurate and timely delivery. • Maintain documents and workflows in Veeva Vault or símilar document management systems, ensuring compliance with applicable regulatory requirements, internal procedures, and templates. Job requirements • MSc or PhD in Pharmacy, Life Sciences, or a related scientific or medical discipline; alternatively, a PharmD or MD. • At least 5 years of relevant medical writing experience within the pharmaceutical, biotechnology, or CRO environment, with a minimum of 3 years of experience supporting pharmacovigilance activities. • Demonstrated experience in authoring or coordinating pharmacovigilance and safety-related documents. • Experience in authoring clinical or regulatory documents such as protocols, clinical study reports, investigator’s brochures, submission documents, or responses to health authority questions. • Practical experience with Veeva Vault, preferably Veeva Safety or Veeva RIM, in regulated document authoring, review, approval, and lifecycle workflows. • Strong knowledge of applicable ICH guidelines, GCP, global pharmacovigilance requirements, and medical writing standards. • Ability to interpret and clearly communicate complex clinical and safety data, with excellent scientific writing skills and strong attention to detail. • Strong document-planning skills and the ability to coordinate input from cross-functional and multicultural stakeholders; excellent written and spoken English. • Experience working on biosimilar programs is desirable. Originally posted on Himalayas