Teva Pharmaceuticals is one of the world’s leading manufacturers of generic medicines, with a robust presence in over 60 countries. Known for producing medications listed on the World Health Organization’s Essential Medicines List, Teva helps millions of people access affordable healthcare every day. With a focus on quality and innovation, the company is committed to transforming healthcare on a global scale. If you are passionate about making a difference in the healthcare industry, Teva offers an excellent opportunity to join their team as a Clinical Research Associate I in Navi Mumbai, India.
Responsibilities in the Job
As a Clinical Research Associate I at Teva, you will play a pivotal role in overseeing the smooth execution of Bioavailability and Bioequivalence (BA/BE) studies. Your key responsibilities will include:
- Managing the data collection, compilation, and review process for research.
- Participating in the Investigational product administration and monitoring adherence to study protocols.
- Ensuring compliance with regulatory standards, including ICH-GCP, GLP, FDA, and internal SOPs.
- Coordinating with pathology labs for screening, post-study, and follow-up sample analysis.
- Participating in subject enrollment for new studies and monitoring their progress.
- Maintaining detailed records of the study process, including drug administration and case report forms.
- Managing study supplies and equipment, and ensuring that all documentation is completed in a timely manner.
- Engaging with study participants and addressing their concerns to ensure compliance with study protocols.
Qualifications
To qualify for this role, you must meet the following educational and experiential requirements:
- A B.Pharm, M.Pharm, or M.Sc. in Clinical Research.
- At least 2-8 years of experience working as a Clinical Research Coordinator at a reputed BA/BE center.
Skills
To succeed in this role, the following skills are essential:
- Attention to Detail: You will be handling sensitive clinical data and need to ensure accuracy in all records.
- Communication: The ability to engage with study participants and address their concerns effectively.
- Organization: Managing multiple aspects of clinical trials requires strong organizational skills.
- Regulatory Knowledge: Understanding of ICH-GCP, GLP, FDA guidelines, and in-house SOPs is crucial.
- Team Collaboration: You will be coordinating with different teams to meet strict timelines for study completion.
How to Apply
If you’re ready to join Teva Pharmaceuticals in making a global impact in healthcare, visit their official careers page or search for the job ID 58562 to apply. Make sure your resume reflects your clinical research experience, and be prepared to discuss how you can contribute to Teva’s mission. If you require any accommodations during the recruitment process, Teva encourages open communication to ensure a smooth and accessible application experience.
