Teva Pharmaceuticals; Clinical Research associate Jobs
Clinical Research Associate I Job vacancies at Teva Pharmaceuticals, Navi Mumbai
Teva Pharmaceuticals, a global leader in the pharmaceutical industry, is seeking a Clinical Research Associate I to ensure compliance with regulations and SOPs in assigned studies.
about TEVA Pharmaceuticals;
Teva is a global pharmaceutical leader and the world’s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world’s largest medicine cabinet to 200 million people daily. We offer a uniquely diverse portfolio of products and solutions for patients, and we’ve built a promising pipeline centred around our core therapeutic areas. We continually develop patient-centric solutions and significantly grow our generic and speciality medicines business through investment in research and development, marketing, business development, and innovation. This is how we improve health and enable people to live healthier lives. Join us on our journey of growth!
Posts: Clinical Research Associates, Clinical Trial Assistant
Clinical Research Associates
- Qualification: M.Pharm
- Experience: 1.5-3 years
• Clinical research associated with exposure to on-site monitoring may apply.
• Open to travel to sites across the country (10-12 days a month) - Location: Seawoods, Mumbai
Clinical Trial Assistant
- Qualification: Fresher with B.Pharm; M.Sc. (Science); M.Sc. (Clinical Research)
- Experience : 0-2 years
- Clinical research coordinator (CRC) experience in hospital clinical trials.
- Must have skills: Clinical Trials, Master file, Dossier & payment release.
Location: Bangalore & Mumbai
Clinical Research Associate Job Description
- Ensure all assigned studies follow SOPs, GCP, and applicable regulations.
- To make all regulatory/ethics submissions as per timelines and to ensure regulatory documents are available, complete, and current.
- Perform study site selection visits with the project manager and medical monitor. Participate in/conduct investigator’s meetings and site initiation visits.
- To identify, define, coordinate, and conduct site study training.
- In coordination with the project manager, provide oversight of all study-related activities.
- To perform regular monitoring visits to the site
- To ensure compliance with ICH-GCP guidelines, local & international regulations (Ex. DCGI, FDA), and applicable SOPs.
Required Qualification for Clinical Research Associate; M Pharm
Function; Research & Development
Sub Function; Clinical Development
Already Working @TEVA?
If you are a current Teva employee, please apply using the internal career site available on “Employee Central.” By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site.
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please get in touch with your local HR/IT partner.
Teva’s Equal Employment Opportunity Commitment
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva’s global policy that equal employment opportunities be provided without regard to age, race, creed, colour, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.
HOW TO APPLY;
Interested candidates may send their CVs to:
Re**********@te**.in
.
Last Date: 15th May 2023
