Clinical Research Scientist I
Location
Bangalore | India
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.
How You'll Spend Your Day - To be qualified by education, experience and training to assume responsibility for proper conduct of the study.
- Comply with requirements of the GCP, EC/Sponsor agreed protocol and Lotus SOP's applicable regulatory requirements and the ethical principles which have their origin in the declaration Of Helsinki
- Review and timely inputs on the protocol (eg dosing information, contradictions, warnings, precautions, adverse events, drug interaction) CRF, ICD 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 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 respectively to perform duties assigned to them.
- Ensuring that all necessary trial related documents are generated and compliant with the protocol.
- Responsible for all clinical or medical aspects of the study hence should personally conduct or supervise the study.
- Brief the volunteer about the study and the related procedures, encouraging the volunteers to ask questions, answering the questions and then obtaining written informed consent and ensure the same is captured audio-visually.
- Enrolling healthy volunteers as per the inclusion / exclusion requirements of the protocol.
- Supervision of activities like check-in, dosing, blood sampling and separation as applicable.
Your Experience And Qualifications - MBBS OR MD
- 2 Years of experience into BABE Studies
Reports To - Manager Clinical Research
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.
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.
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