Job title: Clinical Research Assoc I
Company: Teva Pharma
Job description: Who are we? 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 col
Who are we 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 every day. We offer a uniquely diverse portfolio of products and solutions for patients and we’ve built a promising pipeline centered around our core therapeutic areas. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth! Job Description To ensure all assigned studies follows SOPs, GCP and applicable regulations To do all regulatory/ethics submission as per timelines and to ensure regulatory documents are available, complete and current In coordination with the project manager and/or medical monitor, perform study site selection visits. Participate in/conduct investigator’s meeting and site initiation visits To perform regular monitoring visits to site To verify the case report forms and source data according to the monitoring plan To ensure site level metrics (i.e. 100% IP accountability, 100% informed consent documentation etc.) are tracked and communicated as appropriate Conduct site close out and assure appropriate archival of controlled documents Resolve issues as they affect clinical plan timelines and quality to ensure achievement of goals and objectives at the site level Work in liaison with the finance department in the organization and administration of financial payments to the investigators or relevant local institutions To ensure the compliance to ICH-GCP guidelines, local & international regulations (Ex. DCGI, FDA) and applicable SOP Qualifications . M.Pharm pharmacology / B.Pharm+M.Sc. in Clinical Research . Should have 2-3 Years’ experience of monitoring clinical trials. . Experience in monitoring the clinical trials which includes SIV, SMV, SCV & Site selection visit . Travelling included (10-15 days in a month) across India to various cities 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: The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact 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 opportunity be provided without regard to age, race, creed, color, 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.
Expected salary:
Location: Bangalore, Karnataka
Job date: Sat, 29 Oct 2022 22:16:09 GMT
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