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Clinical Study Coordinator Jobs (NOW HIRING)

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 ...

Element Research Group Inc

Study Coordinator

Minneapolis, MN · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The study coordinator position is a supportive role to study directors conducting nonclinical studies at ERG. Study coordinators will contribute to the organization and execution of the technical ...

Frontage Laboratories

Study Coordinator

Chicago, IL · On-site

$21.64 - $26.45/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Study Coordinator Location: Chicago, IL (on-site) Reports to: Director Laboratory Operations ... Experience supporting Non-GLP and GLP non-clinical toxicology studies is preferred. * Excellent ...

Smithers Group

Study Coordinator

West Trenton, NJ · Hybrid

$60K - $75K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... clinical services for all phases of drug development. PDS works with customers to develop and ... Smithers PDS is seeking a Study Coordinator I or II to join our team in Gaithersburg, MD. The job ...

Smithers Group

Study Coordinator

Gaithersburg, MD · Hybrid

$60K - $75K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... clinical services for all phases of drug development. PDS works with customers to develop and ... Smithers PDS is seeking a Study Coordinator I or II to join our team in Gaithersburg, MD. The job ...

Belcan

Clinical Study Manager

Durham, NC

$56.99 - $71.32/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The Contract Clinical Study Manager provides operational leadership, coordination, and oversight for assigned clinical studies. This role supports the successful execution of study activities in ...

University of Michigan

Study Coordinator

Ann Arbor, MI · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

This position involves coordination of multiple ongoing research studies in children and adults ... clinical setting. * Comfort and experience interacting directly with children (and their parents ...

TalentBurst, Inc.

Clinical Study Manager

Durham, NC

  • Medical

  • Dental

  • Vision

  • Retirement

The Contract Clinical Study Manager provides operational leadership, coordination, and oversight for assigned clinical studies. This role supports the successful execution of study activities in ...

Belcan

Clinical Study Manager

Durham, NC · On-site

$56.99 - $71.32/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The Contract Clinical Study Manager provides operational leadership, coordination, and oversight for assigned clinical studies. This role supports the successful execution of study activities in ...

System One

Clinical Study Manager

Durham, NC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Study Manager Location: Durham, North Carolina Type: 12-month Contract Work Model: Onsite ... Coordinate with internal project team members, CROs, vendors, investigators, and study coordinators ...

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Showing results 21-40

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Clinical Study Coordinator information

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$28K

$67.5K

$116K

How much do clinical study coordinator jobs pay per year?

As of Aug 15, 2026, the average yearly pay for clinical study coordinator in the United States is $67,542.00, according to ZipRecruiter salary data. Most workers in this role earn between $53,500.00 and $78,500.00 per year, depending on experience, location, and employer.

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

AspectClinical Study CoordinatorClinical Research Associate
Required CredentialsTypically a bachelor's degree in health sciences or related field; certifications like CCRP are a plusOften a bachelor's degree in life sciences; certifications like CCRP or RAC are common
Work EnvironmentConducts site visits, manages study activities at clinical sitesMonitors multiple sites remotely or on-site, ensuring protocol compliance
Employer & Industry UsageHospitals, clinics, research sitesPharmaceutical companies, CROs, biotech firms

While both roles support clinical research, Clinical Study Coordinators focus on managing day-to-day site activities, whereas Clinical Research Associates primarily monitor and oversee multiple sites to ensure regulatory compliance and data integrity.

What are some common challenges clinical study coordinators face when managing multiple studies at once?

Clinical Study Coordinators often juggle several studies simultaneously, which requires strong organizational and time-management skills. Challenges include prioritizing tasks, ensuring regulatory compliance across different protocols, and keeping accurate documentation for each study. Effective communication with investigators, sponsors, and participants is essential to prevent misunderstandings and maintain study timelines. Utilizing project management tools and maintaining up-to-date records can help coordinators stay on track and reduce stress.

What are the key skills and qualifications needed to thrive as a clinical study coordinator?

To thrive as a Clinical Study Coordinator, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, often supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, IRB submission processes, and Good Clinical Practice (GCP) certification is highly valued. Strong organizational skills, attention to detail, and effective communication are essential soft skills for coordinating study teams and liaising with stakeholders. These abilities ensure studies are conducted ethically, efficiently, and in accordance with regulatory standards, safeguarding both data integrity and participant safety.
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Clinical Study Coordinator jobs near you
Infographic showing various Clinical Study Coordinator job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $67,542 per year, or $32.5 per hour.

Clinical Study Coordinator

University of Nebraska Medical Center

Omaha, NE • On-site, Remote

$57K - $85K/yr

Full-time

This job post has expired today. Applications are no longer accepted.

University Of Nebraska Medical Center rating

8.5

Company rating: 8.5 out of 10

Based on 15 frontline employees who took The Breakroom Quiz

53rd of 1,059 rated hospitals

Job description

Requisition Details
GENERAL REQUISITION INFORMATION
EEO Statement:
UNMC is an Equal Employment Opportunity Employer, including an equal opportunity employer of protected veterans and individuals with disabilities.
Location
Omaha, NE
Requisition Number:
Staff_14917
Department
Int Med DEM 50000586
Business Unit
College of Medicine
Reg-Temp
Full-Time Regular
Work Schedule
TBD by patient care, research and academic activity
Remote/Telecommuting
No remote/telecommuting opportunity
Position Summary
Coordinate diabetes and endocrine studies. Recruiting patients and maintaining required consents and documentation. Ensures compliance to protocol and IRB approval and provides light clinical and responsible administrative support at UNMC and VAMC for the clinical research activities of the division of DEM (Diabetes, Endocrinology and Metabolism).
Position Details
Additional Information
Posting Category
Healthcare
Working Title
Clinical Study Coordinator
Job Title
Health Care Specialist
Salary Grade
HC23S
Appointment Type
B1 - REG MGR PROF SALARY
Salary Range
$57,000 - $85,500/annual
Job Requisition Begin Date
08/06/2026
Application Review Date
08/14/2026
Review Date Information:
Initial application review will begin on the date provided in the field above. Applications received prior to this review date will be considered. Applications received after the review date may be considered.
Required and Preferred Qualifications
Required Education:
Bachelor's degree
If any degree major/training is required, please specify the type. (NOTE: Concentration and minors are not equivalent to a major)
(Will consider six years education and/or related experience combined of which two years must include post high school education)
Required Experience
2 years
If any experience is required, please specify what kind of experience:
Clinical experience and/or research experience in a clinical or laboratory setting
(Will consider six years education and/or related experience combined of which two years must include post high school education)
Required License
No
If yes, what is the required licensure/certification?
Required Computer Applications:
Microsoft Excel, Microsoft Word, Microsoft Outlook
Required Other Computer Applications:
Required Additional Knowledge, Skills and Abilities:
Ability to work independently and as part of a team;
Ability to accurately follow study protocol guidelines;
Effective verbal and written communication skills;
Attention to detail in completing paperwork and data entry in a timely fashion;
Ability to identify potential problems.
Preferred Education:
Relevant coursework/specialized training
If any degree/training is preferred, please specify the type:
Training related to healthcare, laboratory and/or clinical research.
Preferred Experience:
Preferred License:
Yes
If yes, what is the preferred licensure/certification?:
Phlebotomy certification, or willing to obtain
Preferred Computer Applications:
Microsoft PowerPoint, SAP
Preferred Other Computer Applications:
Electronic Health Records
Preferred Additional Knowledge, Skills and Abilities:
Have prior phlebotomy experience or be willing to be trained.
Have experience in processing blood/serum labs (including shipping), or be willing to be trained.
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https://unmc.peopleadmin.com/postings/99655

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