Job Title: Clinical Research Associate I
Location: Bangalore, India,
Company: Teva Pharmaceuticals
Job ID: 55425
About Us:
At Teva Pharmaceuticals, we’re on a global mission to improve access to affordable healthcare and enhance the quality of life for millions of people. With operations in nearly 60 countries and a diverse workforce, we are proud to be the world’s leading manufacturer of generic medicines.
Our products, many of which are included in the World Health Organization’s Essential Medicines List, are trusted by over 200 million patients worldwide every day. As we continue to grow, we are committed to innovating and finding new ways to make a difference, together with dedicated individuals who share our passion.
Job Description:
As a Clinical Research Associate I at Teva Pharmaceuticals, you will play a crucial role in ensuring the quality and compliance of clinical research activities. Your responsibilities will include:
- Monitoring and Quality Assurance: Overseeing all aspects of study activities from initiation to close-out, including check-in, dosing, sample collection, processing, and final checkout.
- Project Coordination: Collaborating closely with the Project Management Group to meet sponsor requirements and timelines, ensuring adherence to protocols and Good Clinical Practice (GCP) guidelines.
- Documentation and Compliance: Reviewing and maintaining study files, coordinating with the Report Writing Group for timely document submissions, and ensuring all activities comply with regulatory requirements and standard operating procedures (SOPs).
- Ethics and Regulatory Compliance: Coordinating with Ethics Committees for protocol submissions and ensuring all study-related documents are prepared and reviewed according to regulatory standards.
- Audit Support: Participating in internal and external audits by regulatory authorities and sponsors, ensuring all documentation and processes meet audit requirements.
Your Experience and Qualifications:
To succeed in this role, you should possess:
- A Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, Life Sciences, or a related field.
- Fresh graduates or individuals with 1-4 years of experience in Quality Control, Clinical Research Coordination, or a similar role within the pharmaceutical or healthcare industry.
- Strong understanding of Good Clinical Practice (GCP), regulatory requirements, and clinical trial processes.
- Excellent organizational skills, attention to detail, and the ability to work effectively both independently and in a team environment.
- Proficiency in MS Office applications and familiarity with clinical trial management systems (CTMS) is preferred.
Equal Opportunity Employer:
Teva Pharmaceuticals is committed to fostering an inclusive and diverse workplace where all employees feel valued, respected, and empowered. We embrace diversity in all its forms and are dedicated to providing equal employment opportunities regardless of race, religion, gender, disability, or any other legally protected status. If you require accommodations during the recruitment process, please inform us, and we will ensure your needs are met confidentially.
Benefits and Career Development:
Working at Teva Pharmaceuticals offers more than just a job. We provide competitive compensation and benefits packages, including healthcare coverage, retirement plans, and opportunities for professional growth and development. As a global leader in the pharmaceutical industry, we encourage continuous learning and offer resources to support your career advancement.
Join Our Team:
If you are passionate about making a difference in healthcare and are looking for a rewarding career where your skills and dedication can contribute to meaningful outcomes, we invite you to apply for the position of Clinical Research Associate I at Teva Pharmaceuticals. Together, we can continue to innovate and improve lives around the world.
Disclaimer: We strongly advise against paying any third-party individuals or agencies who claim to offer job placements at our company. All job openings are filled based on merit through our official hiring channels. Protect yourself from fraud and ensure that your application is processed securely and fairly by only engaging directly with our official representatives.
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