Teva Pharmaceuticals is hiring for the position of Clinical Research Scientist II in Navi Mumbai, India. This role typically involves designing and implementing clinical trials, analyzing data, and ensuring compliance with regulatory standards. Candidates with experience in clinical research and a relevant scientific background are preferred.
Clinical Research Scientist II
Navi Mumbai, Maharashtra, India
About the job
Who We Are
Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.
How You’ll Spend Your Day
- To be qualified by education, experience and training to assume responsibility for proper conduct of the study.
- Before study start:
- Comply with all applicable regulations, complete required forms.
- Comply with requirements of the GCP, EC/Sponsor agreed protocol and Lotus SOP’s applicable regulatory requirements and the ethical principles which have their origin in the declaration Of Helsinki
- Read and understand the IB or appropriate information on the drug prior to study start.
- Review and timely inputs on the protocol (eg dosing information, contradictions, warnings, precautions, adverse events, drug interaction) CRF, ICD and any other document as required for the study.
- Obtaining ethics committee approval and clarifying the issues / questions raised by the EC.
- Ensure that all study personnel assisting in the trial are aware of their obligations and have been trained on the protocol, study plan and trial related duties and functions respectively to perform duties assigned to them.
- Ensuring that all necessary trial related documents are generated and compliant with the protocol (for e.g vacutainer labels, dosing label study schedule stations).
- Responsible for all clinical or medical aspects of the study hence should personally conduct or supervise the study.
Your Experience And Qualifications
- 0- 2 Years of expereince into Clinical Investigator BABE Studies
- Female preferred
- MBBS