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Mgr Clinical Research

10 - 14 years

0 Lacs

navi mumbai maharashtra

Posted:3 days ago| Platform: Shine logo

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Skills Required

clinical research gcp protocol review informed consent ecsponsor agreed protocol lotus sops ethics committee approval screening activities coordination medical counseling

Work Mode

On-site

Job Type

Full Time

Job Description

As a Manager of Clinical Research at Teva Pharmaceuticals, you will play a crucial role in ensuring the proper conduct of studies related to BA/BE Studies. Your responsibilities will include complying with all applicable regulations, completing necessary forms, and adhering to the GCP, EC/Sponsor agreed protocol, Lotus SOPs, regulatory requirements, and ethical principles. Before the study starts, you will review and provide timely inputs on the protocol, obtain ethics committee approval, and ensure that all study personnel are trained and aware of their obligations. You will be overall responsible for supervising study-related activities, providing timely inputs in the protocol and Informed Consent, and submitting required study documents to the Ethics Committee for approval. Additionally, you will coordinate screening activities in clinical centers, screen volunteers for clinical studies, and decide on subject eligibility based on various parameters. Maintaining accurate records of screening procedures, counseling subjects, and referring them to appropriate facilities when necessary will also be part of your responsibilities. To qualify for this role, you should hold an MBBS or MD degree and have at least 10 years of experience in BA/BE Studies. By joining Teva Pharmaceuticals, you will be part of a global mission to make good health more affordable and accessible, impacting millions of lives worldwide. If you are passionate about making a difference in healthcare and meet the qualifications for this position, we encourage you to apply now and be a part of our team dedicated to improving the lives of others.,

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