Job Summary
The Clinical Research Associate (CRA) plays a pivotal role in overseeing clinical trials. This position involves managing the interaction between sponsors/CROs and investigative sites, ensuring the integrity of data collected during these studies.
Responsibilities
- Monitor the progress of clinical trials to ensure compliance with regulatory guidelines.
- Act as the primary liaison between the sponsor or contract research organization (CRO) and the investigative sites.
- Ensure the accuracy and integrity of data collected during the trial.
- Conduct site visits and audits to assess procedure compliance.
- Collaborate with investigative teams to address and resolve any issues that arise during the study.
Qualifications
- A degree in life sciences, nursing, pharmacy, or a related discipline.
- Approximately 1 to 3+ years of relevant experience in clinical research.
- Strong understanding of clinical trial protocols and regulatory requirements.
- Excellent communication and interpersonal skills for effective collaboration.
- Ability to work onsite and travel as required for monitoring activities.
