Senior Clinical Trials Document Specialist

2 days ago

Belgaum, Karnataka, India beBeeResearch Full time ₹ 9,00,000 - ₹ 15,00,000
Clinical Study Researcher

Delhi and Bangalore locations are open for this role.

  • We seek a highly skilled Clinical Study Researcher to develop key 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 be proficient in translating complex scientific data into clear, regulatory compliant documents that support drug development and approval processes.
  • Strong communication skills and the ability to craft abstracts and manuscripts will be valuable assets in this position.
  • Responsibilities include delivering high-quality documents that contribute to the success of clinical research and regulatory submissions.
  • Key tasks include preparing protocols, CSRs, PIS-ICFs and CRFs, understanding study objectives, designing protocols, preparing and reviewing SOPs, and communicating with stakeholders.
Required Skills and Qualifications
  • Developing high-quality clinical trial documents.
  • Translating complex scientific data into clear documents.
  • Crafting abstracts and manuscripts.
  • Effective communication with stakeholders.
  • Regulatory compliance knowledge.
Benefits

This role offers the opportunity to work on high-profile clinical trials, collaborate with cross-functional teams, and contribute to the advancement of drug development.

About This Opportunity

This is a unique chance to apply your expertise and passion for clinical research to drive innovation and improve patient outcomes.

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