Teva Pharma Clinical Research Associate Job For Pharma, Apply Online
Clinical Research Assoc I
Date: Dec 10, 2024
Location: Navi Mumbai, India, 400706
Company: Teva Pharmaceuticals
Job Id: 58562
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
- Overseeing the smooth running of BA/BE studies.
- Collecting, compiling, completing, and reviewing data obtained from research.
- Informing participants about the study during the ICF process.
- Getting involved in the Investigational product administration process.
- Acting as a custodian and monitoring of research participants to ensure adherence to study rules.
- Adhering to research regulatory standards and in-house SOPs.
- Adhering to ethical standards like ICH-GCP and GLP.
- Maintaining detailed records of studies as per FDA and other required guidelines, including things such as drug administration and subject-specific case report forms.
- Coordinating with the pathology laboratory regarding screening, post-study, and follow-up sample analysis.
- Participating in subject enrollment efforts for new BA/BE studies.
- Ensuring that the necessary supplies and equipment for a study are available before the initiation of the study.
- Engaging with study staff for timely completion of study documentation to meet stringent timelines of project submission.
- Collecting data as required by the protocol. Assuring timely completion of Case Report Forms.
- Maintaining study timelines.
- Completing study documentation and maintaining study files in accordance with requirements as per in-house SOPs and procedures including, but not limited to, consent forms, source documentation, case report forms, and investigational material accountability forms (if required).
- Engaging with subjects and understanding their concerns.
Your experience and qualifications
- B. Pharm, M. Pharm, or M.Sc. (Clinical Research).
- At least 2-8 years of experience as a Clinical Research Coordinator in a reputed BA/BE center.
Link to apply: APPLY ONLINE HERE
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