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Clinical Studies Coordinator Jobs (NOW HIRING)

City of Hope

Clinical Study Coord

Duarte, CA · On-site

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 ...

City of Hope

Clinical Study Coord

Duarte, CA

Clinical Study Coordinator - Clinical Research (On-Site)-Duarte Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer ...

City of Hope

Clinical Study Coord

Duarte, CA

Clinical Study Coordinator - Clinical Research (On-Site)-Duarte Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer ...

City of Hope

Clinical Study Coord

Duarte, CA

Clinical Study Coordinator - Clinical Research (On-Site)-Duarte Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer ...

City of Hope

Clinical Study Coordinator

Duarte, CA

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 ...

University of Utah

Clinical Study Coordinators

Campus, IL · On-site

$48K - $56K/yr

... Coordinator Helps with the logistical and administrative aspect of clinical trials and studies, ensuring adherence to protocols and regulatory requirements. Help facilitate participant recruitment ...

City of Hope

Clinical Study Coord

Duarte, CA

Clinical Study Coordinator - Clinical Research (On-Site)-Duarte Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer ...

City of Hope

Clinical Study Coord

Duarte, CA · On-site

Clinical Study Coordinator - Clinical Research (On-Site)-Duarte Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer ...

City of Hope

Clinical Study Coord

Duarte, CA · On-site

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 ...

City of Hope

Clinical Study Coordinator

Duarte, CA

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 ...

Apex Systems

Clinical Study Coordinator

Phoenix, AZ

As Clinical Study Coordinator, you will get hands on experience planning and managing research ... Daily activities will include: -Set up studies and get all needed materials and documents in order ...

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Clinical Studies Coordinator information

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How much do clinical studies coordinator jobs pay per hour?

As of May 28, 2026, the average hourly pay for clinical studies coordinator in the United States is $28.65, according to ZipRecruiter salary data. Most workers in this role earn between $20.67 and $34.13 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Studies Coordinator, and why are they important?

To thrive as a Clinical Studies Coordinator, you need a strong understanding of clinical research protocols, regulatory compliance, and often a bachelor's degree in a health-related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as CCRC or CCRP are typically required. Attention to detail, organizational skills, and effective communication with study participants and research teams are standout soft skills. These abilities are crucial to ensure the integrity, efficiency, and regulatory compliance of clinical research studies.

What are some common challenges faced by Clinical Studies Coordinators, and how can they effectively manage them?

Clinical Studies Coordinators often encounter challenges such as balancing multiple studies simultaneously, ensuring strict adherence to regulatory protocols, and maintaining clear communication among diverse stakeholders. To manage these effectively, coordinators should develop strong organizational skills, utilize project management tools, and foster collaborative relationships with investigators, sponsors, and study participants. Regular training on regulatory requirements and proactive problem-solving can also help mitigate issues and keep studies on track.

What are Clinical Studies Coordinators?

Clinical Studies Coordinators are professionals who manage and oversee clinical research trials, ensuring they are conducted according to regulatory guidelines and study protocols. They handle tasks such as recruiting and screening participants, collecting and managing data, and communicating with investigators, sponsors, and regulatory bodies. Their work is essential in advancing medical knowledge and ensuring the safety and integrity of clinical trials. Clinical Studies Coordinators often work in hospitals, research institutions, or pharmaceutical companies, collaborating with a multidisciplinary research team.

What is the difference between Clinical Studies Coordinator vs Clinical Research Associate?

AspectClinical Studies CoordinatorClinical Research Associate
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusOften requires a bachelor's or master's degree in life sciences; certifications like CCRP or RAC are common
Work EnvironmentCoordinates daily activities of clinical trials at sites or research centersMonitors clinical trials at multiple sites, ensuring compliance and data integrity
Employer & Industry UsageUsed by hospitals, research centers, and pharmaceutical companiesPrimarily employed by pharmaceutical companies, CROs, and biotech firms

While both roles support clinical trials, Clinical Studies Coordinators focus on managing site activities and participant coordination, whereas Clinical Research Associates primarily monitor trial progress across multiple sites to ensure regulatory compliance and data quality.

More about Clinical Studies Coordinator jobs
What cities are hiring for Clinical Studies Coordinator jobs? Cities with the most Clinical Studies Coordinator job openings:
What are the most commonly searched types of Clinical Studies jobs? The most popular types of Clinical Studies jobs are:
What states have the most Clinical Studies Coordinator jobs? States with the most job openings for Clinical Studies Coordinator jobs include:
Clinical Studies Coordinator jobs near you
Infographic showing various Clinical Studies Coordinator job openings in the United States as of May 2026, with employment types broken down into 13% As Needed, 54% Full Time, 8% Part Time, and 25% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $59,597 per year, or $28.7 per hour.
Clinical Study Coord

Clinical Study Coord

City of Hope

Duarte, CA • On-site

Full-time

Posted 7 days ago

City Of Hope rating

8.4

Company rating: 8.4 out of 10

Based on 84 frontline employees who took The Breakroom Quiz

33rd of 864 rated healthcare providers

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.


 

Qualifications - External
Qualifications - External

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.

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About City of Hope

Sourced by ZipRecruiter

City of Hope is an independent biomedical research and treatment organization for cancer, diabetes and other life-threatening diseases. Founded in 1913, City of Hope is a leader in bone marrow transplantation and immunotherapy such as CAR T cell therapy. City of Hopes translational research and personalized treatment protocols advance care throughout the world. Human synthetic insulin, monoclonal antibodies and numerous breakthrough cancer drugs are based on technology developed at the institution. AccessHope, a subsidiary launched in 2019 serves employers and their health care partners by providing access to City of Hopes specialized cancer expertise. City of Hope is ranked among the nations Best Hospitals in cancer by U.S. News & World Report and received Magnet Recognition from the American Nurses Credentialing Center. Its main campus is located near Los Angeles, with additional locations throughout Southern California and in Arizona.

Industry

Hospitals

Company size

1,001 - 5,000 Employees

Headquarters location

Duarte, CA, US

Year founded

1913

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