Job Summary
The Clinical Research Associate plays a vital role in supporting and managing clinical trials. This position is contingent and operates on a day shift from 8:15 AM to 6:30 PM. The ideal candidate will ensure adherence to regulatory standards and maintain the quality of the research being conducted.
Responsibilities
- Oversee the conduct of clinical trials to guarantee compliance with the prescribed protocols.
- Monitor patient recruitment and retention efforts throughout the study.
- Conduct site visits to collect and verify data from trial sites.
- Prepare and review clinical documentation, including reports and regulatory submissions.
- Assist in resolving any issues that arise during the study process.
- Maintain accurate and detailed records of clinical activities.
- Collaborate closely with investigators and study sponsors for effective communication.
Qualifications
- A degree in life sciences or a related field.
- Previous experience in clinical research is highly desirable.
- Knowledge of Good Clinical Practice (GCP) guidelines.
- Strong analytical skills and attention to detail.
- Excellent communication abilities, both written and verbal.
- Proficient in the use of data management systems and clinical trial software.
