Job Summary
The Clinical Research Associate (CRA) plays a pivotal role in the management and oversight of clinical trials. This position involves ensuring that studies are conducted in compliance with regulatory requirements and study protocols, ultimately contributing to the advancement of medical knowledge and patient care.
Responsibilities
- Coordinate and monitor clinical trials, ensuring adherence to protocols and regulatory guidelines.
- Conduct regular site visits to evaluate the progress of studies and the performance of Investigators.
- Ensure that the integrity of data collected is maintained throughout the study phases.
- Provide training and support to site staff to assure proper implementation of protocols.
- Prepare and review reports related to study activities, contributing to submission documents for regulatory bodies.
Qualifications
- Bachelor’s degree in life sciences or a related field is required, with relevant experience in clinical research preferred.
- Strong understanding of Good Clinical Practice (GCP) and regulatory requirements.
- Excellent interpersonal and communication skills, essential for collaboration with various stakeholders.
- Ability to manage multiple projects simultaneously and work effectively under pressure.
- Proficient in using electronic data capture systems and Microsoft Office applications.
