Zydus Research Centre Released Job Openings On 04/06/2022.Zydus Cadila is one of the India’s leading healthcare companies and a global healthcare provider with a strength all along the pharmaceutical value chain. The groups state-of-the-art manufacturing infrastructure is spread across the five states Gujarat, Maharashtra, Goa, Himachal Pradesh and Sikkim. Out of which, six facilities are USFDA approved. Zydus Lifesciences is headquartered in Ahmedabad, India, After a journey of growth spanning 27 years as Cadila Healthcare Ltd. and the Zydus Group, we have evolved and transformed ourselves in response to the changing times.
Vacancy Details:
Zydus Research Centre Recruiting Graduates with 2 to 4 years experience for Clinical Research Associate, Clinical Trial Associate Position.Complete Details for the Clinical Research Associate, Clinical Trial Associate as follows.
Important Details :
- Job Location: Ahmedabad
- No of Vacancies:NA
- Details of Salary: NA
- Opening date for online Application: 04/06/2022
- Mode of application :Walk In
- Time And Venue : 5th June, 9 am to 2 pm
PTC Sigma, Behind Iskon Temple, Opp. BRTS Bus Stop, Bopal Ambali Road, Ahemdabad.
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Job Description/Skills Required
- We are recruiting for our innovation hub, Zydus Research Centre at Ahmedabad
- We are looking for a Clinical Research Associate with the following requirements:
- The job requires site monitoring, site management, quality check at site, managing site and investigator relationships, assisting and contributing in project delivery, ensuring compliance with ICH GCP, meeting regulatory requirements, training the site staff and keeping regular contacts with investigators to track the course of the study.
- We are also looking for a Clinical Trial Associate with the following requirements:
- The job requires assisting project manager for end to end activities in clinical trial, handling CDA, undertaking investigators, CTA and other clinical trial related documents, maintaining the trial master file (TMF)/site master file (SMF) in compliance with ICH GCP and SOPs.
- The candidates are also required to do shipment/distribution and track clinical trial supplies. support investigational product management team for IP shipment and communicate with the CRA, CRC and investigators who are related to the assigned projects.