Job Summary
The Clinical Research Associate (CRA) plays a crucial role in the management and execution of clinical trials. This position involves overseeing the progress of clinical studies to ensure they are conducted according to protocol, comply with regulatory guidelines, and meet the overall objectives of the study. The CRA serves as a key link between the study sponsor and the clinical sites, ensuring that data integrity and participant safety are maintained throughout the research process.
Responsibilities
- Monitor clinical trial sites to guarantee compliance with the clinical protocol and regulatory requirements.
- Conduct site initiation, monitoring, and closeout visits as part of the clinical trial management process.
- Evaluate site performance and provide necessary training and support to site staff.
- Maintain accurate documentation, and manage trial supplies and subject recruitment efforts.
- Resolve issues that may arise during the study while enhancing communication between all parties involved.
- Coordinate with the project manager and other team members to ensure timelines and deliverables are met.
Qualifications
- Bachelor’s degree in Life Sciences or a related field.
- Experience in clinical research or related work is preferred.
- Knowledge of Good Clinical Practice (GCP) and regulatory requirements.
- Strong organizational, communication, and interpersonal skills.
- Ability to travel to clinical sites as required.
- Proficient in using clinical trial management software and Microsoft Office Suite.
