Job Summary
The Clinical Research Associate (CRA) plays a vital role in overseeing clinical trials, ensuring compliance and maintaining communication between sponsors, Contract Research Organizations (CROs), and investigative sites. The CRA is instrumental in safeguarding the integrity of clinical data, ensuring that all aspects of the study meet regulatory standards.
Responsibilities
- Monitor the progress of clinical trials to ensure adherence to regulatory guidelines.
- Facilitate effective communication between the sponsor/CRO and investigative sites.
- Ensure data integrity and quality throughout the study lifecycle.
- Conduct site visits and evaluate site performance regularly.
- Assist in preparing reports and documentation related to clinical trials.
Qualifications
- Education in life sciences, nursing, pharmacy, or a related field.
- Approximately 1–3+ years of experience in clinical research.
- Strong understanding of clinical trial processes and regulatory requirements.
- Excellent communication and interpersonal skills.
- Ability to work onsite in New Jersey.
