Clinical Research Scientist II

About the job

Who We Are

Together were on a mission to make good health more affordable and accessible to help millions around the world enjoy healthier lives. Its 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 worlds leading manufacturer of generic medicines and the proud producer of many of the products on the World Health Organizations Essential Medicines List. Today at least 200 million people around the world take one of our medicines every single day. An amazing number but were always looking for new ways to continue making a difference and new people to make a difference with.

How Youll Spend Your Day

• To be qualified by education experience and training to assume responsibility for proper conduct of the study.
• Before study start:
• Comply with all applicable regulations complete required forms.
• Comply with requirements of the GCP EC/Sponsor agreed protocol and Lotus 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 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 (for e.g vacutainer labels dosing label study schedule stations).
• Responsible for all clinical or medical aspects of the study hence should personally conduct or supervise the study.

Your Experience And Qualifications

• 0 2 Years of expereince into Clinical Investigator BABE Studies
• Female preferred
• MBBS

Tevas Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Tevas 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 Tevas 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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Remote Work :

No