Clinical Research Jobs

Teva Pharmaceuticals Recruiting For Clinic Subject Care Coordinator


Teva Pharmaceuticals is looking to hire Clinic Subject Care Coordinator .Interested and eligible candidates can send their resume..Teva is a global pharmaceutical leader and the world’s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world’s largest medicine cabinet to 200 million people every day..The eligibility criteria as follows.

Vacancy details :

Company Name : Teva Pharmaceuticals
Department : Clinical Research
Designation : Clinic Subject Care Coordinator
No. of Vacancies : : Not Disclosed
Location :Navi Mumbai,
Qualification :B. Pharm, M. Pharm or M.Sc
Experience :04-06+
Salary : Not Disclosed


Job description:-.

  • To monitor and perform Quality Check of all study activities from check-in, dosing, sample collection, processing, segregation, transfer and till checkout. Co-ordinate with Project management Group (PMG) for compliance with the sponsor requirements and timelines.Provide periodic review on status of study files up to archival of files. Co-ordinate with Report Writing Group for the movement of files to the concerned department and ensuring to maintain timelines.Compilation of study data and review of clinical reports. Coordinate with the Ethics Committee for submission of protocol and other study related documents.To perform QC of ICF, compensation chart and review of CRF (versus Protocol), other study related documents prior to EC submission. To ensure that all the activities are performed by the delegated staff personnel in compliance with the EC approved protocol, GCP and relevant SOP’s and applicable regulatory requirement. Handling of monitor’s visits, maintaining of site visit log, resolution of all queries raised by the monitor/sponsor during his/ her site visit.To carry out other responsibilities as and when assigned by the management. Retrospective review of study documents to ensure adherence to required SOPs and regulatory requirements. To ensure all appropriate entries after documentation.

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