Job Summary
The Clinical Research Associate II plays a vital role in ensuring the smooth operation and efficiency of clinical trials. This position requires a skilled individual who can oversee study sites, manage compliance with regulatory standards, and facilitate communication between all stakeholders involved in the research process. The role emphasizes a hybrid working model, combining both remote and on-site responsibilities depending on study requirements.
Responsibilities
- Monitor clinical trial activities to ensure adherence to protocols and regulations.
- Conduct site evaluations, initiation visits, and routine monitoring visits.
- Maintain meticulous documentation and provide regular updates on trial progress.
- Assist in training site staff and ensure they are well-informed about study protocols.
- Act as a primary liaison between the study sites, sponsors, and other relevant parties.
Qualifications
- Bachelor’s degree in life sciences or a related field.
- Previous experience as a Clinical Research Associate, preferably in a hybrid role.
- Strong understanding of clinical trial processes and regulatory requirements.
- Excellent communication and interpersonal skills.
- Proficiency in data entry and tracking software related to clinical research.
Cedars-Sinai Medical Center - Los Angeles 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.
