Intas Released Job Openings On 22/12/2022.Intas Experience spanning three decades in healthcare, with a wide range of formulations to meet the needs of ailing humanity, Intas Pharmaceuticals headquartered at Ahmedabad (India), is now a force to reckon with, in the global pharma horizon. With expertise in a range of formulations, from tablets to injectables to newer drug delivery systems, Intas is currently ranked 17th among the Indian Pharma majors..Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for Intas Recruitment 2021 are provided below. Interested and eligible candidates can submit application along with resume.
Vacancy Details:
Intas Recruiting B.Pharma,M.Pharm,Any Postgraduates with 02-07 Years 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:22/12/2022
- 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: Sun Pharma Hiring FRESHERS And Experienced
Job Description/Skills Required
RESPONSIBILITIES:
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.
Click here for Official notification and Apply
