Job Information
Teva Pharmaceuticals Clinical Research Scientist II in Bangalore, India
Clinical Research Scientist II
Date: Apr 18, 2024
Location:
Bangalore, India, 560064
Company: Teva Pharmaceuticals
Job Id: 54919
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 ensure that the clinical study is conducted according to the approved protocol and applicable regulatory requirements.
To protect rights, safety and welfare of subjects.
Management of Investigational Products.
To ensure that sufficient number of qualified medical, paramedical, and clerical staff is available to conduct the study.
To ensure that all staff assisting in study is adequately trained on the protocol, investigational product and their duties.
To be aware of regulatory requirements and acceptable standards for conduct of clinical trial and protection of human subjects.
To ensure that the data is complete, accurate, legible and internally consistent and maintain timelines.
To take all study related medical decisions.
To ensure that adequate medical care is provided to the subject for any adverse event, including clinically significant laboratory values.
In case of health related problems, the investigator should inform the subject's primary physician about the subject's participation in the trial, if the subject has a primary physician and if the subject agrees to the primary physician being informed.
To Review AE / SAE reporting forms after it is filled by the physician / designee.
To Provide timely inputs on the protocol
To conduct study in compliance with protocol approved by IEC, sponsor and regulatory agencies whenever applicable.
To document and explain any deviation from the approved protocol.
To ensure initiation of study and proper conduct of study in compliance with the study protocol and GCP requirements and communicate with IEC about any deviation in the protocol.
Your experience and qualifications
MBBS OR MD
2 - 4 years of experience into Principal Investigator
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.
EOE including disability/veteran