Clinical Study Coordinator

Cancer Treatment Centers of America, Inc.; Duarte, Northern (CA, KY); Hybrid; USD 65,000 - 90,000; Full time

Benefits offered by this job

Comprehensive benefits

Job summary

City of Hope seeks a full-time, on-site Clinical Study Coordinator at the Duarte Medical Center to support oncology clinical trials from First in Human to Phase III. You will recruit participants, obtain informed consent, coordinate trials, manage data, and ensure regulatory compliance in a fast-paced environment.

The ideal candidate has a Bachelor’s degree in Science/Health, 2+ years of clinical research experience, and relevant certifications (ACRP/SOCRA, IATA, GCP, HSP, BLS).

Qualifications

• Bachelor’s degree in Science, Health or related field required; 3 additional years may substitute for education.
• Minimum of 2 years research or clinical experience
• ACRP or SOCRA certification within 1 year of employment
• IATA, GCP, HSP, and BLS training within 1 month of employment

Responsibilities

• Understand and apply FDA, OHRP, GCP/ICH, HIPAA regulations 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 understanding and compliance.
• Monitor eligibility, safety, and protocol adherence; report adverse events promptly.
• Pursue ongoing education and maintain required certifications/licensure.

Skills

Communication skills

Regulatory knowledge

Attention to detail

Education

Bachelor’s degree in Science/Health or related field

ACRP or SOCRA certification

IATA certification

GCP certification

HSP training

BLS certification

Tools

Regulatory systems

Job description

Clinical Study Coordinator - Clinical Research (On-Site)

Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope's growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today.

Duarte Medical Center seeks a full-time, on-site Clinical Study Coordinator to support oncology clinical trials. Under the supervision of the Director, Clinical Research, this patient-facing role 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 .

To learn more about our Comprehensive Benefits, please .