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Study Document Coordinator

2 weeks ago

Bengaluru, Karnataka, India beBeeCoordination Full time ₹ 1,04,000 - ₹ 1,30,878

Job Title: Study Document Coordinator

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This role involves coordinating the processing of study documents, ensuring adherence to client and study requirements as well as ICON SOPs/WPs and relevant regulations.

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You will be working closely with study teams and other TMF staff to fulfill your responsibilities effectively. This includes completing departmental projects as assigned, maintaining study files per study/client requirements and ICON SOPs/WPs, and handling document receipt and processing tasks.

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Key Responsibilities include:

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  • Receiving, reviewing, scanning, indexing, and archiving study documents.\
  • Liaising with study project teams, staff, clients, and management to ensure effective communication.\
  • Maintaining accurate records and filing systems for study documents.\
  • Providing information for client and departmental status reports as requested.\
  • Participating in audits and document archiving activities as needed.\
  • Assisting in training sessions related to responsibilities.\
  • Addressing project issues with clients as directed by the Manager.\
  • Undertaking special projects or additional duties as requested.\
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Requirements:

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  • 1-15 years of experience in Trial Master File (TMF) coordination with a strong knowledge of clinical study documents.\
  • Excellent communication and organizational skills.\
  • Ability to work effectively in a team environment.\
  • Bachelor's Degree in Life Sciences preferred.\
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Benefits:

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As a Study Document Coordinator, you will have the opportunity to work on various studies and contribute to the success of our projects. You will also have access to ongoing training and development opportunities to enhance your skills and knowledge.

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Join us in this exciting role and take the first step towards a rewarding career in Clinical Research