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Medical Information Writer

Propharma
Propharma
0-2 years
Not Disclosed
Remote
10 March 2, 2026
Job Description
Job Type: Full Time 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

Medical Information Writer – PharmD Graduate Opportunity

Location: India (Remote / Hybrid as per business requirements)
Employment Type: Full-Time
Job Requisition ID: JR 9127
Department: Medical Information

About the Organization

ProPharma is a global life sciences consulting organization supporting biotechnology, pharmaceutical, and medical device companies across the entire product lifecycle. Through its advise–build–operate model, the organization delivers specialized expertise in regulatory sciences, clinical research, pharmacovigilance, medical information, quality & compliance, and R&D technology. With over 20 years of experience, ProPharma partners with clients to accelerate innovation while ensuring regulatory compliance and patient safety.

About the Role

ThePharmaDaily.com invites applications for the position of Medical Information Writer in India. This full-time opportunity is ideal for PharmD graduates who are passionate about scientific writing, literature research, and medical communications within the pharmaceutical industry.

The Medical Information Writer is responsible for drafting technically accurate, regulatory-compliant responses such as medical information letters and Frequently Asked Questions (FAQs) used to address inquiries received by Medical Information teams. This role involves conducting structured literature reviews, synthesizing scientific data, and developing concise, reader-friendly documentation aligned with global compliance standards.

Comprehensive training, mentoring, and supervision will be provided to support professional development in medical writing and scientific communications.

Key Responsibilities

Medical Writing & Service Delivery

  • Conduct comprehensive literature searches using Medline and other scientific databases

  • Draft technical medical information letters, FAQs, and related scientific documents

  • Condense complex clinical and pharmacological data into clear, concise, and readable responses

  • Update existing standard response documents to ensure scientific accuracy and regulatory relevance

  • Ensure all written materials comply with Standard Operating Procedures (SOPs) and client-specific Working Practices

Quality Assurance & Compliance

  • Perform quality checks on own work and assist in reviewing basic documents prepared by team members

  • Maintain compliance with pharmaceutical industry regulations and professional guidelines

  • Adhere to confidentiality, data privacy, and internal compliance policies

  • Maintain professional communication standards with clients and internal stakeholders

  • Support additional responsibilities as assigned by management

Eligibility & Qualifications

  • PharmD graduate (mandatory)

  • Strong understanding of pharmacology, therapeutic areas, and evidence-based medicine

  • Excellent written communication and scientific writing skills

  • Ability to interpret and summarize clinical literature accurately

  • High proficiency in computer applications, including Microsoft Office

  • Strong organizational and time management skills

Experience Required

  • 0–2 years of experience in Medical Writing, Medical Information, Pharmacovigilance, Clinical Research, or related pharmaceutical domains preferred

  • Fresh PharmD graduates with strong academic performance and interest in scientific writing are encouraged to apply

Core Competencies

  • Exceptional attention to detail and accuracy

  • Strong analytical and critical thinking skills

  • Ability to manage multiple assignments within defined timelines

  • Professional collaboration and team-oriented approach

  • Commitment to regulatory compliance and data privacy standards

Work Model

Remote working is supported; however, hybrid collaboration may be encouraged for candidates located within commuting distance of office locations, subject to agreement with management.

Diversity & Equal Opportunity

The organization promotes diversity, equity, and inclusion, fostering a professional environment where employees are empowered to contribute and grow. All applications are personally reviewed by the recruitment team, and candidates receive a formal update regarding their application outcome.

Application Process

Applications will be assessed based on educational qualifications, writing proficiency, and relevant pharmaceutical exposure. Shortlisted candidates will be contacted for further evaluation and interview rounds.

This role is ideal for PharmD professionals seeking to establish a long-term career in Medical Writing, Scientific Communications, Regulatory-Compliant Documentation, and Global Medical Information Services within the life sciences industry.