Medical Writer - Scientific Services

Role Overview

The Medical Writer plays a pivotal role in the development of high-quality scientific content tailored for healthcare professionals, medical affairs teams, and other stakeholders. This role requires a strong foundation in medical science, excellent writing skills, and the ability to translate complex data into clear, engaging, and accurate communication materials. The Medical Writer will be responsible for content development across a range of deliverables and collaborate closely with cross-functional teams including editorial, design, client services, and project management.

Key Responsibilities

Scientific Content Development

Lead the creation of scientifically accurate, engaging, and compliant content including slide decks, manuscripts, advisory board reports, training modules, and digital assets.

Interpret and synthesize data from clinical trials, publications, and regulatory documents.

Ensure content adheres to client objectives, brand guidelines, and relevant compliance standards (e.g., GPP, ICMJE).

Review and edit content for clarity, consistency, scientific accuracy, and tone.

Client Stakeholder Collaboration

Participate in client meetings to understand project goals and provide scientific input.

Present content strategy and scientific messaging to clients and internal stakeholders.

Build strong relationships with medical affairs teams, KOLs, and subject matter experts.

Project Management Quality Assurance

Manage multiple projects simultaneously, ensuring timely delivery and high-quality output.

Collaborate with project managers to define timelines, scope, and resource needs.

Maintain version control and documentation for all content developed.

Strategic Input Innovation

Contribute to content strategy and planning for new and existing clients.

Stay updated on therapeutic area developments, industry trends, and publication standards.

Support business development efforts by contributing to proposals, pitches, and sample content.

Qualifications Experience

Advanced degree in life sciences or equivalent (PhD, MD, PharmD preferred).

Minimum 5+ years of experience in medical writing within a medical communications agency or pharmaceutical company.

Medical Writing Editing Course from a reputed university will be an added advantage.

Strong understanding of clinical research, drug development, and medical affairs.

Proven ability to write for diverse audiences including HCPs, patients, and internal stakeholders.

Ability to work independently and collaboratively in a fast-paced environment.

Preferred Skills

Experience of working in different therapeutic areas

Knowledge of digital content formats and platforms.

Exposure to publication planning and scientific congress support.

Understanding of global compliance and regulatory standards.