Lambda Therapeutic Research Released Job Openings On 14/07/2022.We, Lambda Therapeutic Research Limited are a leading global Clinical Research Organization (CRO) headquartered in Ahmedabad – India, with facilities and operations in Mumbai (India), Mehsana (India), Toronto (Canada), Warsaw (Poland), London (UK) and USA with approximate 750 employees located in our facilities across the globe.
Vacancy Details:
Lambda Therapeutic Research Recruiting B.Sc,B.Pharma,Any Postgraduate Candidates with 02 to 07 years of Experience for Clinical research Scientist Position.Complete Details for the Clinical research Scientist as follows.
Important Details :
- Location :Kolkata, New Delhi, Hyderabad/Secunderabad, Pune, Ahmedabad ( Gota) , Chennai, Bangalore/Bengaluru, Delhi / NCR, Mumbai (All Areas)
- No of Vacancies:08
- Details of Salary: ₹ 5,00,000 – 10,00,000 P.A.
- Opening date for online Application:14/07/2022
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
Related Job : FRESHERS: Production,QA,QC,Accounts and Finance Departments Openings At Amara Labs
Job Description/Skills Required
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.
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