Job Summary
The position of Clinical Research Associate involves overseeing and coordinating clinical studies at various investigative sites. This role ensures that the trials comply with established protocols, standard operating procedures (SOPs), International Conference on Harmonisation – Good Clinical Practice (ICH-GCP), and other relevant regulations.
Responsibilities
- Monitor the execution and progress of clinical trials at assigned sites.
- Ensure studies are conducted in accordance with the protocol and regulatory requirements.
- Record and report study data accurately and in a timely manner.
- Maintain compliance with SOPs and ICH-GCP guidelines throughout the study process.
Qualifications
- Experience in clinical research and familiarity with regulatory requirements.
- Strong organizational and communication skills.
- Ability to work collaboratively in a team-oriented environment.
- Detail-oriented with a focus on quality and accuracy in reporting.
