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Principal Medical Writer – Remote, India

8+ years
Not Disclosed
10 Nov. 26, 2025
Job Description
Job Type: Hybrid Remote 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

Principal Medical Writer – Remote, India

 [Location / Remote, if applicable]

Location: [City, Country / Remote]
Job Type: Full-Time
Category: [Job Category, e.g., Clinical Research, Pharmacovigilance, Medical Affairs]
Job ID: [Job ID]
Work Model: [On-site / Remote / Hybrid]


About the Role

[Company Name] is seeking a highly skilled [Job Title] to join our [department/team name]. The role involves [brief description of core responsibilities, e.g., managing clinical research projects, pharmacovigilance data, or program development] to drive impactful outcomes in [therapeutic area or business focus].

This position offers an opportunity to work in a global, collaborative environment, contributing to [company’s mission, e.g., life-changing therapies, cutting-edge research, or innovative healthcare solutions].


Key Responsibilities

  • Lead and manage [primary responsibility, e.g., clinical programs, data analysis, safety reporting, project coordination] across [scope, e.g., global teams, multiple studies, or cross-functional departments].

  • Collaborate with internal and external stakeholders to ensure alignment, compliance, and timely delivery of objectives.

  • Develop, review, and validate [documents, reports, or systems] to meet regulatory and operational standards.

  • Monitor progress, identify risks, and implement solutions to maintain project quality and timelines.

  • Contribute to process improvements, training, and mentoring of junior staff.

  • Ensure compliance with [relevant regulations, e.g., GCP, SOPs, FDA/EMA standards].


Required Experience & Qualifications

  • Bachelor’s or Master’s degree in [relevant field, e.g., Life Sciences, Nursing, Computer Science, Pharmacology].

  • Minimum [X] years of relevant experience in [specific domain, e.g., clinical research, pharmacovigilance, programming, data management].

  • Strong knowledge of [technical skills, e.g., Oracle Argus, SQL, clinical trial processes, regulatory compliance].

  • Proven ability to manage multiple priorities in a fast-paced, global environment.

  • Excellent communication, problem-solving, and analytical skills.


Preferred Qualifications

  • Advanced knowledge in [therapeutic area or specialized skill, e.g., hepatology, renal research, oncology].

  • Experience with global projects, regulatory submissions, or multinational teams.

  • Leadership or mentoring experience is highly valued.


Why Join [Company Name]?

[Company Name] is committed to [mission statement, e.g., advancing healthcare, developing innovative therapies, improving patient outcomes globally]. We provide an inclusive, collaborative, and growth-focused environment where your contributions have global impact.

Equal Opportunity Employer: [Company Name] provides equal employment opportunities for all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other legally protected status.


SEO Keywords Optimized: [Job Title] India, [Job Category] Remote, [Company Name] Careers, Global Clinical Research Jobs, Pharmacovigilance / Clinical Safety Careers.