Clinical Research Scientist II

1 month ago

Bengaluru, Karnataka, India Teva Pharmaceuticals Full time
Who we are

We aim to improve global health by making it more affordable and accessible, uniting people from diverse backgrounds in nearly 60 countries. Join us and be part of the world's leading manufacturer of generic medicines, playing a vital role in providing essential healthcare products to millions every day. Our work impacts lives, and we are always seeking fresh perspectives to drive further positive change.

How you'll spend your day
  • Ensure the clinical study adheres to approved protocols and regulatory standards.
  • Protect subjects' rights, safety, and well-being.
  • Manage Investigational Products.
  • Coordinate qualified staff to conduct the study effectively.
  • Train staff on protocols, products, and responsibilities.
  • Stay updated on regulatory requirements for clinical trials.
  • Oversee accurate and timely data collection.
  • Make medical decisions related to the study.
  • Provide necessary medical care for subjects in case of adverse events.
  • Communicate with subjects' primary physicians when required.
  • Review and report adverse events.
  • Contribute inputs to protocol development.
  • Ensure compliance with approved protocols and regulations.
  • Document and explain any deviations from protocols.
  • Initiate and conduct studies following protocol and GCP requirements.
  • Ensure proper communication with relevant agencies regarding protocol adherence.
Your experience and qualifications
  • Medical Degree (MBBS OR MD)
  • 2 - 4 years experience as a Principal Investigator.
Teva's Equal Employment Opportunity Commitment

Teva Pharmaceuticals upholds equal employment opportunities for all. We believe in a diverse and inclusive workplace, free from discrimination based on various factors. If you require any accommodations during the recruitment process, please inform us, and your needs will be handled with utmost confidentiality to ensure a smooth candidate experience.

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