Teva Pharmaceuticals Bangalore Hiring Clinical Research Associates

Teva Pharmaceuticals Clinical Research Associates Jobs

Are you looking for an opportunity to advance your career in clinical research? Teva Pharmaceuticals in Bangalore is hiring Clinical Research Associates. This role offers a chance to work with the world’s leading manufacturer of generic medicines and make a significant impact on global health.

About Teva Pharmaceuticals

Teva Pharmaceuticals is committed to making good health more affordable and accessible. With operations in nearly 60 countries and a diverse workforce, Teva is dedicated to improving the lives of millions worldwide. The company’s mission is to continue making a difference by providing quality medicines and healthcare solutions.

Job Role: Clinical Research Associate

As a Clinical Research Associate at Teva Pharmaceuticals in Bangalore, you will play a critical role in ensuring the quality and compliance of clinical studies. Your responsibilities will include monitoring study activities, coordinating with project management and ethics committees, and performing quality checks on study documentation.

Key Responsibilities

• 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.
• Any discrepencies/ Deviations to be informed to Team Leader and Manager (if Required).
• Ensuring quality by reviewing all study related documents like Regulatory binder, Raw data binders, Case Report Form binders, Study close out report, Sample Case record form, Study updates, screening examination record.
• Full participation in internal and external audits by sponsors and other oversight entities such as FDA, EU, ANVISA.
• Review of SDTM & Clinic tables data with the source document.
• To verify the calibration and verification of instruments/equipment.
• To review the execution of Qualification Protocol & Qualification Summary Report
• To prepare & review standard operating procedures as delegated by PI or HOD or Manager.
• Ensuring quality by reviewing all study related documents like Study Protocol and amendments, Informed consent form, Clinical Study Report, Electronic Trial master file, Study synopsis.
• Providing compliance for reviewed all study related documents like Study Protocol and amendments, Informed consent form, Clinical Study Report, Electronic Trial master file, Study synopsis.
• Review clinical study report to ensure that the reports are in accordance with SOPs, protocol and applicable regulatory requirements, and that the reported results accurately reflect source data of the clinical studies.
• To coordinate with the user department and medical writing department for clinical study reports.

Qualifications

• Education: B.Pharm, M.Pharm, or M.Sc. in a relevant field.
• Experience: 2-4 years in Quality Control (QC) or as a Clinical Research Coordinator (CRC) or in the Nursing department of clinical research.
• Skills: Strong attention to detail, analytical skills, and the ability to work both independently and as part of a team.

How to Apply

If you meet the qualifications and are ready to take on a challenging and rewarding role, apply now to join Teva Pharmaceuticals as a Clinical Research Associate in Bangalore. Apply here.