Highly Skilled Clinical Research Document Developer

2 days ago

Kota, Rajasthan, India beBeeClinicalResearch Full time ₹ 9,00,000 - ₹ 12,00,000

About Our Clinical Research Team

We are seeking a highly skilled Medical Writer and Clinical Study Researcher to join our clinical research team. This key role will involve developing high-quality clinical trial documents that support drug development and approval processes.

Key Responsibilities:

  • Developing high-quality key clinical trial documents, including protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs).
  • Translating complex scientific data into clear, regulatory compliant documents.
  • Crafting abstracts and manuscripts, demonstrating strong scientific communication skills.
  • Delivering high-quality, accurate, and well-structured documents that contribute to the success of clinical research and regulatory submissions.
  • Preparing protocols, CSRs, PIS-ICFs, and CRFs.
  • Understanding study objectives and designing protocols.
  • Preparing and reviewing SOPs.
  • Communicating with stakeholders to ensure effective and complete documentation within the timeline.

Requirements:

  • Proficiency in developing clinical trial documents.
  • Strong scientific writing and communication skills.
  • Ability to understand complex scientific data and translate it into clear documents.
  • Experience in crafting abstracts and manuscripts.
  • Commitment to delivering high-quality documents.

What We Offer:

  • A dynamic and collaborative work environment.
  • Ongoing training and professional development opportunities.
  • The chance to work on challenging projects and make a meaningful contribution to the field of clinical research.

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