What are the responsibilities and job description for the Clinical Research Coordinator (CRC) position at ORANGE COUNTY RESEARCH CENTER?
Job Description
Job Description
We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our exceptional team. The ideal candidate will be responsible for coordinating and overseeing clinical trials, ensuring compliance with all regulatory requirements, and contributing to the success of our ongoing and future studies in our beautiful office located in Lake Forest, CA.
Responsibilities include :
- Coordinate all aspects of clinical trials, including participant recruitment, enrollment, and follow-up.
- Prepare and manage study documentation, and ensure accurate data entry in accordance with protocol and GCP guidelines.
- Maintain regular communication with Principal Investigator, Sponsors, and Regulatory bodies.
- Oversee patient scheduling, informed consent process, and trial logistics.
- Monitor patient progress and report any adverse events promptly.
- Collaborate with multidisciplinary teams to ensure trial objectives are met efficiently.
- Ensure compliance with ethical standards and regulatory requirements throughout the study.
We offer a competitive benefits package including :
Qualifications :
OCRC is an equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and / or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law.
