We, Lambda Therapeutic Research Limited are a leading global Clinical Research Organization (CRO) headquartered in Ahmedabad – India, with facilities and operations in Mehsana (India), Toronto (Canada), Warsaw (Poland), London (UK) and Pittsburgh (USA), Las Vegas (USA) and Fargo (USA) with approximate 1500+ employees located in our facilities across the globe.

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Delivering the best is accomplished by hiring the best. They are the pillars that fulfill every quality promise that we make. That’s why, at Lambda, we are always looking for qualified and energetic individuals with an unquenchable drive for excellence on every front, which is expected and rewarded.

The Lambda Family as we call it is also a closely-knit group sharing not just professional, but personal bonds through various commemorative, cultural, and societal enrichment activities throughout the year.

Position: Sr Clinical Research Associate/CRA – Clinical Trails

Location: Ahmedabad

Job Description:

  • Perform Site Identification and conduct Feasibility Studies.
  • Perform Site Selection Visit, Site Initiation Visits in accordance with the protocol, and other applicable regulatory guidelines including local regulatory guidelines.
  • Perform Site Monitoring Visit and Site Close-Out Visit in accordance with the protocol and other applicable regulatory guidelines including local regulatory guidelines.
  • Send Follow Up letters to sites and submit Visit Reports to the Clinical Team Leader/
  • Project Manager as required.
  • Keep a close association with the site(s) for Patient Recruitment, Patient Follow Up, and protocol-related activities.
  • Act as a communication link between the Sponsor and the site.
  • Maintain accurate and timely sponsor/site correspondence and communication.
  • Attend Investigators Meeting.
  • Training of Investigators on Protocol and other applicable regulatory guidelines including local regulatory guidelines.
  • Ethics Committee Submission
  • Help in preparation of Regulatory Binder.
  • Maintain updated Site Files and collection of the essential documents and project-related documents during the site visits and maintain Central Clinical File.
  • CRF retrieval as per the project instructions.
  • Coordinate and distribute Clinical Study Material to study sites.
  • Archival of study documents.

Qualification: B.Sc, B.Pharma

Experience: 2-7 Years

Salary: 3,50,000 to 8,50,000 INR CTC/PA

Contact Details:

careers@lambda-cro.com,  rushabhbshah@lambda-cro.com

 

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