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 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!

• Overseeing the smooth running of BA/BE studies.
• Collecting, compiling, completing and reviewing data obtained from research.
• Informing participants about study during ICF process.
• Get involved in the Investigational product administration process.
• To act as a custodian and monitoring of research participants to ensure adherence to study rules.
• Adhering to research regulatory standards and in-house SOPs.
• Adhering to ethical standards like ICH-GCP and GLP.
• Maintaining detailed records of studies as per FDA and other required guidelines, including things such as drug administration and subject specific case report forms.
• Co-ordination with pathology laboratory regarding screening, post study and follow up sample analysis.
• Participating in subject enrollment efforts for new BA/BE studies.
• Ensuring that the necessary supplies and equipment for a study are available before initiation of study.
• Engaging with study staff for timely completion of study documentation to meet stringent timelines of project submission.
• Collects data as required by the protocol. Assures timely completion of Case Report Forms.
• Maintains study timelines.
• Completes study documentation and maintains study files in accordance with requirements as per in house SOPs and procedures including, but not limited to, consent forms, source documentation, case report forms and investigational material accountability forms (if required).
• Engaging with subjects and understanding their concerns.

Qualifications

Education: B. Pharm, M. Pharm or M.Sc. (Clinical Research).

Experience: At least 4-5 years of experience as a Clinical Research Coordinator in reputed BA/BE center.

Function

Research & Development

Sub Function

Clinical Development

Already Working @TEVA?

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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.