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About Company

The ideal candidate must have a strong background in medical and scientific writing, especially medico-marketing/marketing communications. They must have a deep understanding of the pharmaceutical, life sciences, medical devices, and healthcare industries and the ability to understand complex information and create clear and engaging content.

Position Name :

Medical Writer

Organization :



M.Sc, M.Pharm, ph.D


4+ years


CTC: 8.10 LPA



As a Senior Medical Communications Content Writer, they will play a critical role in our efforts to deliver high-quality communication materials that support our clients’ goals.

Key Responsibilities:

Content Development:

  • Understand project briefs and guide content writers and cross-functional teams.
  • Research, write, and edit various medical communication materials, including scientific manuscripts, medical marketing collateral, and educational content.
  • Knowledge of different marketing collaterals and best practices.
  • Create content outlines and storylines, aligning with business/marketing objectives and campaign plans.
  • Review and proof-read content for quality and accuracy.
  • Create various types of collaterals:Print materials – Brochures, POS material, posters, newsletters, patient cards, etc.
    Digital materials – Emails, iDetails, E-learning modules, social media posts, slides, PPTs, etc.
    Audio-visual materials – Educational videos, MoA Videos, 2D/3D animations, etc.

Scientific Accuracy:

  • Ensure the accuracy, integrity, and scientific rigor of all content.
  • Stay up-to-date with the latest healthcare, pharmaceutical, and therapeutic developments.

Audience Adaptation:

  • Customize content for diverse target audiences, including healthcare professionals, patients, and regulatory authorities, maintaining scientific integrity and regulatory compliance.


  • Collaborate with cross-functional teams, including medical experts, graphic designers, digital coding experts, project managers, clients, and client servicing teams.
  • Liaise directly with clients and external stakeholders as required.

Regulatory Compliance:

  • Adhere to industry guidelines, regulatory requirements, and ethical standards.
  • Ensure all content meets the highest standards of quality and compliance.

People & Project Management:

  • Manage multiple projects simultaneously, ensuring timely and within-scope completion.
  • Work closely with the content writing team; review content created by team members; train, mentor, and guide new team members.

Feedback Integration:

  • Incorporate feedback from clients and internal stakeholders to continually improve and refine content.

Content Approval Support:

  • Aware of different types of submissions for content approval by clients/regulatory bodies/healthcare authorities, preferably in US, UK, EU, Middle East, and Asian markets.
  • Hands-on experience with Veeva Vault PromoMats is essential; other submission processes are an added advantage.

Qualifications & requirements:

  • Master’s degree in a relevant field (e.g., life sciences, pharmacy) is required. Advanced degrees (e.g., PhD) are a plus.
  • 4+ years of experience in medical communications, medical writing, or a related field.
  • Strong understanding of the pharmaceutical and healthcare industries, including knowledge of clinical trials, drug development, regulatory processes, and marketing activities.
  • Exceptional writing and editing skills, with the ability to convey complex scientific concepts clearly and engagingly.
  • Proficiency with industry-specific software and tools (e.g., Microsoft Office, EndNote, and reference management software, Veeva Vault, Aprimo, etc).
  • Strong attention to detail and ability to work independently or as part of a team.
  • Knowledge of industry guidelines, including ICH-GCP, PhRMA, and CONSORT, is a plus.
  • Flexible to work between 2 PM to 11 PM IST.

Application Link