Job title: Clinical Research Scientist II
Company: Teva Pharmaceuticals
Job description: Company Info
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
- Responsible for planning, conduct, execution, documentation and reporting of bioequivalence
- and pharmacokinetic studies in conformance to GCP standards, SOPs, and applicable regulators.
- Communication with PMG
- Tracking of projects
- Feasibility of studies
- Discussion with team for ensuring meeting time lines
- Interview for recruitment of staff
- SOP review and Preparation
- Involving in sponsor and regulatory audits
- Ensuring the site availability, experts’ availability and technical staff for execution of studies
- Involving in regulatory audits
- To ensure that all professional and technical personnel involved in
- the conduct of the study have job descriptions and records of training, qualification and experience, which support their ability to undertake the tasks assigned to them
- Monitoring of Clinical staff and allocation of duties.
- Review of protocols, informed consent documents (ICF) and case record forms (CRF) for clinical studies and getting approvals from IEC.
- Review of medical records and ascertain eligibility of subjects
- Obtain written informed consent from study subjects
- Carry out medical examination of volunteers for screening prior to clinical studies or as required
- Supervision of dispensing and retention of investigational products.
- Manage medical emergencies
- Responsible to ensure proper reporting of adverse events
- Supervise the safety related activities of clinical staff during the study conduct.
- Carry out medical examination of volunteers for screening prior to clinical studies or as required.
Qualifications
4-5 years with MBBS/MD
Function
Research & Development
Sub Function
Clinical Research
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: Navi Mumbai, Maharashtra
Job date: Thu, 24 Mar 2022 05:26:29 GMT
Apply for the job now!
