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Senior Medical Content Specialist

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Bengaluru, Karnataka, India beBeeMedicalWriter Full time ₹ 20,00,000 - ₹ 25,00,000
Job Summary:

The ideal candidate must have a strong background in medical and scientific writing, especially in the medico-marketing/marketing communications field.

Key Responsibilities:

  • Content Development: Read and understand project briefs, guide content writers and cross-functional teams on scope of work. Research, write, and edit a wide range of medical communication materials, including scientific manuscripts, medical marketing collateral, and educational content.
  • Scientific Accuracy: Ensure the accuracy, integrity, and scientific rigor of all content by staying up-to-date with the latest developments in healthcare, pharmaceuticals, and relevant therapeutic areas.
  • Audience Adaptation: Write/adapt/customize the content to diverse target audiences, including healthcare professionals, patients, and regulatory authorities, while maintaining scientific integrity and regulatory compliance.
  • Collaboration: Collaborate with cross-functional teams to produce cohesive and effective communication materials. Liaise directly with clients and external stakeholders as required for the project.
  • Regulatory Compliance: Adhere to industry guidelines, regulatory requirements, and ethical standards to ensure all content meets the highest standards of quality and compliance.

Qualifications & Requirements:

  • A Master's degree in a relevant field (e.g., life sciences, pharmacy) is required. Advanced degrees (e.g., PhD) are a plus.
  • Minimum of 5+ years of experience in medical communications, medical writing, or a related field and 2+ years as people manager/team lead. This is mandatory.
  • A strong understanding of the pharmaceutical and healthcare industry, 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 in a clear and engaging manner.
  • Proficiency with industry-specific software and tools (e.g., Microsoft Office, EndNote, and reference management software).
  • Knowledge of industry guidelines, including ICH-GCP, PhRMA, and CONSORT, is a plus.