The Senior Clinical Research Associate (Sr. CRA) at ProTrials Research, Inc. is responsible for monitoring and managing clinical trials to ensure they are conducted, recorded, and reported in accordance with protocols, standard operating procedures (SOPs), ICH GCP, and all applicable regulatory requirements. This position plays a vital role in the successful execution of clinical research projects with a commitment to care, integrity, and excellence.
What You'll Do
- Ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH GCP, and all applicable regulatory requirements
- May be required to travel up to 65%
What We're Looking For
- Experience in clinical research monitoring
- Knowledge of ICH GCP and regulatory requirements
- Ability to travel up to 65%
Team & Environment
- Valued, supported, and empowered team members
- Collaborative community
- Commitment to making a meaningful impact on global health
- Passion for advancing clinical research with care, integrity, and excellence
Work Mode
Up to 65% travel required
