Job Summary
The Clinical Research Associate (CRA) plays a pivotal role in the clinical research process by ensuring that clinical trials are conducted in compliance with regulatory standards. This position involves monitoring clinical studies and maintaining the quality of data collected, which ultimately supports the safety and efficacy evaluations of new medical treatments.
Responsibilities
- Oversee clinical trial sites and ensure adherence to the study protocol, regulatory requirements, and Good Clinical Practice (GCP).
- Conduct regular site visits to monitor progress, facilitate training, and resolve any issues that arise.
- Review and verify clinical documentation and data entry for accuracy and completeness.
- Communicate effectively with investigators and site personnel to ensure smooth study operations.
- Prepare and present reports for regulatory authorities and the internal study team.
Qualifications
- Bachelor’s degree in life sciences, nursing, or a related field.
- Proven experience in clinical research, specifically in monitoring clinical trials.
- Strong understanding of clinical trial regulations and GCP standards.
- Excellent organizational, communication, and interpersonal skills.
- Ability to work independently and manage multiple priorities effectively.
Piper Companies provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
