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.
Henry Ford Health System 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.
