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Job Description

Responsibilities:

  • Review protocol and provide suggestions ​
  • Respond to queries/ clarifications from EC/ IRBs
  • Answer medical questions from sites or project team
  • Respond to queries from sites with regard to protocol
  • Attend drug safety meetings/ external meetings
  • Patient eligibility review
  • Review AE/ SAEs
  • Protocol training to site staff, CRAs etc
  • Attend, participate/ present in investigator meetings

Qualification: MBBS/ MD qualification 

Eligibility:

  • 3 year+ of clinical trial experience
  • Familiar with clinical trials operations
  • Good English communication skills
  • Proficiency in using Microsoft office

More Info

Job Type:
Employment Type:
Open to candidates from:
Indian

About Company

A part of the Tata group, India's largest multinational business group, TCS has over 500,000 of the world’s best-trained consultants in 46 countries. The company generated consolidated revenues of US $22.2 billion in the fiscal year ended March 31, 2021, and is listed on the BSE (formerly Bombay Stock Exchange) and the NSE (National Stock Exchange) in India. TCS' proactive stance on climate change and award-winning work with communities across the world have earned it a place in leading sustainability indices such as the MSCI Global Sustainability Index and the FTSE4Good Emerging Index.

Job ID: 106303855

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