Senior Clinical Content Developer

3 days ago

Gulbarga, Karnataka, India beBeeClinicalResearch Full time ₹ 9,00,000 - ₹ 12,00,000
Medical Content Specialist

Delhi and Bangalore based positions are currently open.

  • We are seeking a highly skilled Medical Content Specialist to develop high-quality clinical trial documents, including protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs).
  • The ideal candidate will have expertise in translating complex scientific data into clear, regulatory compliant documents that support drug development and approval processes.
  • Additionally, they should be able to craft compelling abstracts and manuscripts, demonstrating strong scientific communication skills.
  • The selected individual will deliver accurate, well-structured documents that contribute to the success of clinical research and regulatory submissions.
  • Responsibilities include preparing protocols, CSRs, PIS-ICFs, and CRFs, as well as understanding study objectives and designing protocols.
  • They will also prepare and review SOPs, ensuring effective documentation within given timelines.
Key Skills and Qualifications:
  • Proficiency in developing high-quality clinical trial documents
  • Excellent translation and communication skills
  • Ability to work with complex scientific data
  • Strong scientific writing and editing skills
  • Experience with document preparation and review
Why This Role is Important:

This role plays a crucial part in the success of our clinical research initiatives. By delivering high-quality documents, you will directly contribute to the advancement of medical research and the development of new treatments.

How to Apply:

Interested candidates should submit their application for this position. We look forward to reviewing your qualifications and experience.

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