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Associate Clinical Research Coordinator Jobs (NOW HIRING)

City of Hope

Assoc Clinical Research Coord

Duarte, CA · On-site

$25.50 - $33.75/hr

Associate Clinical Research Coordinator 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 ...

City of Hope

Assoc Clinical Research Coord

Duarte, CA · On-site

$25.50 - $33.75/hr

Associate Clinical Research Coordinator 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 ...

NYULMC

Associate Clinical Research Coordinator

New York, NY · On-site

$26.50 - $35.25/hr

The Non-therapeutic Oncology Associate Clinical Research Coordinator (NT aCRC) is an active participant in the coordination of oncology clinical research studies from research planning and throughout ...

NYULMC

Associate Clinical Research Coordinator

New York, NY · On-site

$26.50 - $35.25/hr

The Non-therapeutic Oncology Associate Clinical Research Coordinator (NT aCRC) is an active participant in the coordination of oncology clinical research studies from research planning and throughout ...

Mayo Clinic

Associate Clinical Research Coordinator

Phoenix, AZ · On-site

$24.25 - $32.25/hr

Coordinates non-therapeutic (i.e. minimal risk, survey, chart review) clinical research protocols ... HS Diploma with at least 3 years of experience OR Associate's degree/college Diploma/Certificate ...

Bannerhealth

$20.50 - $27.25/hr

The Associate Clinical Research Coordinator will support our team of CRC's and RN's with research related functions, as well as oversee their own portfolio of long term follow up studies. Primarily ...

Quality Clinical Research,

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Clinical Research Coordinator

Omaha, NE · On-site

$24 - $29/hr

Clinical Research Coordinator Location: Omaha NE Position Type: Full-Time, On-Site We are seeking a professional, organized, and motivated Clinical Research Coordinator to join our Omaha office. The ...

Urgent

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How much do associate clinical research coordinator jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for associate clinical research coordinator in the United States is $28.69, according to ZipRecruiter salary data. Most workers in this role earn between $23.32 and $31.01 per hour, depending on experience, location, and employer.

What skills and qualifications are needed to thrive as an associate clinical research coordinator?

To thrive as an Associate Clinical Research Coordinator, you need a background in life sciences or a related field, knowledge of clinical trial processes, and an understanding of regulatory requirements. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and possibly certifications like SOCRA or ACRP are typical technical assets. Strong organizational skills, attention to detail, and effective communication help you excel in coordinating studies and interacting with diverse teams. These skills ensure studies are conducted accurately, ethically, and efficiently, supporting both compliance and successful trial outcomes.

What are the primary challenges an associate clinical research coordinator might face during a clinical trial?

One common challenge for Associate Clinical Research Coordinators is managing multiple tasks and tight timelines, as they often handle patient recruitment, data entry, and regulatory documentation simultaneously. Additionally, ensuring strict adherence to study protocols and regulatory guidelines can be complex, especially when unexpected issues arise with participants or data collection. Effective communication with the research team, principal investigators, and study participants is essential to navigate these challenges successfully and maintain the integrity of the trial.

What is an associate clinical research coordinator?

Associate Clinical Research Coordinators are entry-level professionals who assist in the planning, implementation, and management of clinical trials and research studies. They support lead coordinators and principal investigators by handling tasks such as recruiting participants, collecting and entering data, ensuring regulatory compliance, and maintaining study documentation. Their role is crucial in ensuring that clinical trials run smoothly and adhere to ethical and legal standards. Associate Clinical Research Coordinators often work in hospitals, universities, or research organizations, and their work helps advance medical knowledge and patient care.
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Associate Clinical Research Coordinator jobs near you
Infographic showing various Associate Clinical Research Coordinator job openings in the United States as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $59,666 per year, or $28.7 per hour.

Assoc Clinical Research Coord

City of Hope

Duarte, CA • On-site

$25.50 - $33.75/hr

Full-time

Re-posted 26 days ago

City Of Hope rating

8.4

Company rating: 8.4 out of 10

Based on 89 frontline employees who took The Breakroom Quiz

25th of 887 rated healthcare providers

Job description

Associate Clinical Research Coordinator
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. 
Reporting to the Supervisor of Clinical Research Division at City of Hope Duarte Medical Center, we offer multiple full-time on-site positions within the Clinical Trial Office (CTO). As an Associate Clinical Research Coordinator (ACRC), you'll play a pivotal role in ensuring the integrity of research studies. From data abstraction and completion of case report forms to facilitating sponsor visits and maintaining audit-ready data, your responsibilities encompass meticulous coordination. You'll oversee the readiness of laboratory kits and patient-specific equipment for visits, ensuring strict compliance with research protocols. Your duties extend to coordinating biospecimen collection, transportation, and shipment while collaborating with Biospecimen Coordinators to maintain meticulous records. With a focus on maintaining updated patient data in the clinical research management system, your contribution will be integral to the success of diverse research endeavors at City of Hope.
As a successful candidate, you will: 
  • Work under the supervision of the Manager, Study Investigators, and Senior Manager, with a focus on protocol-specific duties required by research protocols.
  • Ensure adherence to protocol for specimen collection and sponsor-specific equipment procedures, guaranteeing accurate documentation.
  • Identify and promptly communicate important protocol and data management issues to the supervisor.
  • Uphold Good Clinical Practices, FDA Rules, NIH guidelines, HIPAA regulations, ICH guidelines, and institutional policies for clinical trials.
  • Enter accurate and up-to-date data into the clinical research management system (CRMS) for study patients.
  • Collaborate within the clinical research team, maintaining positive and effective communication while seeking ways to improve job performance and surroundings.
Qualifications - External
Qualifications - External
Qualifications - External
Qualifications - External
Qualifications - External
Qualifications - External

Your qualifications should include: 

  • Bachelor’s degree. Experience may substitute for minimum education requirements. (Associate Degree plus minimum of 2 years of experience).
  • At least one year of experience related to the management and conduct of oncology clinical trials in an academic setting, or six months experience as a Project Coordinator or Biospecimen Coordinator in the CTO.
  • Working knowledge of clinical trials, Federal, State, and Local Regulations, IRB requirements, consent form and protocol development.
  • Good Clinical Practice (GCP) and Health Information Portability and Accountability ACT (HIPAA)-to be provided by COH if not already completed.

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 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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