Job Description:

Job Description CRA / Sr CRA (Clinical Trial)
Required Experience 2 Years to 8 Years
Required Qualification Any Science Graduate
Location - Ahmedabad, Delhi, Mumbai, Lucknow, Jaipur, Nasik, Nagpur, Pune, Kolkata, Bangalore, Hyderabad,
Chennai
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 site (s) for Patient Recruitment, Patient Follow Up, and protocol related activities
Act as a communication Link between 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

Profile Summary:

Employment Type : Full Time
Eligibility : Any Graduate
Industry : Healthcare, Biotechnology/Pharmaceutical/Medicine
Functional Area : Bio Tech/R&D/Scientist
Role : Clinical Research
Salary : As per Industry Standards
Deadline : 18th Mar 2020

Key Skills:

Company Profile:

Company
Lambda Therapeutic Research Ltdarfix

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