Clinical Study Coord

 involves coordinating First in Human to Phase III and Investigator-Initiated Trials. Responsibilities include patient recruitment, informed consent, trial coordination, data management, and regulatory compliance. The position requires in-depth knowledge of clinical trial regulations, strong organizational skills, and the ability to collaborate with investigators and clinical staff in a fast-paced environment.
As a successful candidate, you will:
• Understand and apply federal regulations (FDA, OHRP, GCP/ICH, HIPAA) and institutional policies.
• Follow and execute clinical trial protocols and procedures.
• Coordinate participant recruitment, informed consent, and care.
• Communicate with participants, investigators, and sponsors to ensure clear understanding and compliance.
• Monitor and document participant eligibility, safety, and protocol adherence, and report adverse events promptly.
• Pursue continuous education and training opportunities, staying updated with the latest clinical research information, and maintain necessary certifications and licensure.

Your qualifications should include:
• Bachelor's degree in Science, Health or related field from an accredited university; 3 additional years of experience plus the minimum experience requirement may substitute for minimum education.
• Minimum of 2 years research or relevant clinical experience
• ACRP or SOCRA certification within 1 year of employment
• International Air Transport Association (IATA) within 1 month of employment
• Good Clinical Practice (GCP) within 1 month of employment
• Human Subjects Protection (HSP) within 1 month of employment
• Basic Life Support (BLS) within 1 month of employment

City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.

City of Hope is an equal opportunity employer. To learn more about our commitment to diversity, equity, and inclusion, please click here.

To learn more about our Comprehensive Benefits, please CLICK HERE.