Job Description
Who we are
Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.
The opportunity
- Responsible for screening activities including obtaining informed consent from volunteers, performing General physical & medical examination (GPE), Review of ECG & X-Ray reports, Review of Lab Reports, Review of ABA & UDS reports.
How you’ll spend your day
- Obtaining study specific informed consent from eligible Volunteers.
- Comply with the requirements of the GCP, EC/sponsor agreed protocol, in-house SOPs, applicable regulatory requirements, and the ethical principles which have their origin in the declaration of Helsinki.
- Read and understand the IB or appropriate information on the drug prior to study start.
- Review and provide timely inputs on the protocol (for ex. dosing information, contraindications, warnings, precautions, adverse events, drug interactions) ICF, CRF and any other document as required for the study.
- Obtaining ethics committee approval and clarifying the issues/questions raised by the EC.
- Ensure that all the study personnel assisting in the trial are aware of their obligations and have been trained on the protocol, study plan and trial related duties and functions to perform the duties assigned to them.
- Ensure that all necessary trial related documents are generated and compliant with the protocol (For e.g., vacutainer labels, dosing label, study schedule, stations).
- Responsible for all clinical or medical aspects of the study and should personally conduct and supervise the study.
- Brief the volunteer about the study and the related procedures, encouraging the volunteers to ask questions, answering the questions, obtaining written informed consent and to ensure that the same is captured audio- visually.
- Enrolling healthy volunteers as per the inclusion /exclusion requirement of the protocol.
- Supervision of activities like check-in, dosing, blood sampling and separation as applicable.
- Maintain accountability of the Investigational product and clinical supplies from receipt till study completion.
- Ensure that the queries (if any) related to the IP are resolved before dosing.
Your experience and qualifications
- MBBS OR MD Qualified
- Freshers OR 2 years of experience into Clinical Investigator for a female BABE Studies.
Make a difference with Teva Pharmaceuticals 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. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.
