Research Scientist

1 day ago

Rajkot, Gujarat, India beBeeclinical Full time ₹ 20,00,000 - ₹ 25,00,000

Clinical Study Researcher plays a vital role in the development and approval of drugs. The successful candidate will be responsible for creating key clinical trial documents, including protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs).

Key Responsibilities:
  • Document Creation: Proficient in translating complex scientific data into clear, regulatory compliant documents.
  • Protocol Design: Understanding the study objectives and designing the protocol to ensure effective documentation within the timeline.
  • Procedure Preparation: Preparing and reviewing Standard Operating Procedures (SOPs) to maintain compliance.
  • Stakeholder Communication: Communicating with stakeholders to ensure complete and accurate documentation.

You will also be responsible for preparing abstracts and manuscripts, demonstrating strong scientific communication skills. Your commitment to delivering high-quality documents will contribute to the success of clinical research and regulatory submissions.

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