Medical Writer - Medical Affairs - 5+ Years - Gurgaon

Medical Writer - CDMA - Medical Affairs / Scientific Communications - 5+ Years - Gurgaon

Location - Gurgaon

Summary-

Medical Writer with 5+ years of experience

Your Future Employer-

scientific communications, medical affairs, and research-driven content creation

Responsibilities-

Literature Reviews & Evidence Mapping

• Conduct comprehensive secondary research using databases such as PubMed, Embase, and Cochrane Library.
• Analyze and interpret clinical/scientific data to extract actionable insights.
• Stay updated on medical and regulatory trends across OTC and Rx domains.

Medical & Scientific Content Development

• Research, write, edit, and review scientific materials across multiple formats.
• Deliver literature reviews, manuscripts, abstracts, posters, slide decks, white papers, and guideline summaries.
• Ensure scientific accuracy, clarity, and compliance with global guidelines (ICMJE, CONSORT).

Content Review & Quality Assurance

• Review and verify references to ensure plagiarism-free, factual content.
• Maintain templates and styles aligned with industry standards.
• Ensure accurate and impactful data presentation.

Project Execution

• Understand and define client requirements, timelines, and deliverables.
• Manage multiple projects with high attention to quality and compliance.
• Collaborate with internal teams, including graphics and medical writing colleagues.

Other Contributions

• Mentor junior team members and contribute to knowledge-sharing.
• Demonstrate strong collaboration, professionalism, and organizational values.

Requirements-

Must Have:

• 5+ years of experience in

  medical/scientific writing

  .
• MBBS / BDS / PhD / Masters in Pharmacy or a related field.
• Strong understanding of pharmaceuticals, OTC, and consumer healthcare.
• Expertise in scientific terminology, clinical studies, and evidence synthesis.
• Proficiency in MS Office and online research tools.
• Excellent written/verbal communication and attention to detail.

Good to Have:

• Familiarity with

  regulatory documentation

  for US/EU markets.
• Knowledge of

  reference management tools

  (EndNote, Mendeley, Zotero).
• Exposure to

  data visualization, text mining, or storytelling tools

  .
• Experience with statistical packages (SPSS, R, SAS, GraphPad Prism).

What is in it for you-

• Opportunity to work on

  global healthcare and pharmaceutical projects

  .
• Blend of

  scientific research, writing, and storytelling

  .
• Collaborative culture with strong mentoring and learning opportunities.
• A role where scientific excellence and creativity meet.

Reach us-

megha.rajput@crescendogroup.in