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TMF Specialist

  1. India
2024-109687
  1. ICON Strategic Solutions
  2. Clinical Trial Management

About the role

This vacancy has now expired. Please click here to view live vacancies.

TMF Specialist is to perform all duties related to the timely processing of essential and non-essential clinical trial documents to facilitate study startup, drug shipment,  eTMF maintenance and support eTMF inspection readiness activities

 

Location : Bangalore/Chennai


EXPERIENCE & SKILLS

  • Ability to interact with Clinical and Regulatory team regarding the receipt, analysis, classification and disposition of documents
  • Preferred: knowledge of “Essential Documents” Clinical Trial Documentation
  • Good verbal and written communication skills (English and local) 
  • Attention to detail and ability to multi-task
  • Strong problem solving, time management, and organizational skills
  • Proficient in use of MS office software including Word, Excel, Access, Share Point & Outlook

 


  • Bachelor’s degree in Sciences required
  • Preferred: 2 Years’ experience in Pharmaceutical or Contract Research Organization
List #1

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In traditional clinical trials, patients must attend regular check-ins at hospitals or clinics but fully remote decentralised clinical trials (DCTs) and hybrid trials limit this by replacing the

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In traditional clinical trials, patients must attend regular check-ins at hospitals or clinics. This is subject to change with an increase in decentralised clinical trials (DCTs).

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