Clinical Documentation Specialist

3 days ago


Udaipur, Rajasthan, India beBeeClinicalDocumentation Full time ₹ 12,00,000 - ₹ 15,00,000

Job Title: Clinical Documentation Specialist

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  • Responsible for developing high-quality clinical trial documents, including protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs).
  • Skilled in translating complex scientific data into clear, regulatory compliant documents that support drug development and approval processes.
  • Experienced in crafting abstracts and manuscripts, demonstrating strong scientific communication skills.
  • Committed to delivering accurate and well-structured documents that contribute to the success of clinical research and regulatory submissions.

Key Responsibilities:

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  • Preparation and review of SOPs.
  • Communication with all stakeholders to ensure effective and complete documentation within the timeline.
  • Understanding the study objectives and designing the protocol.

Requirements:

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  • Proficient in MS Office Suite.
  • Strong analytical and problem-solving skills.
  • Excellent written and verbal communication skills.

Benefits:

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  • Opportunity to work on challenging projects.
  • Collaborative and dynamic work environment.
  • Professional growth and development opportunities.


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