1

Clinical Studies Coordinator Jobs (NOW HIRING)

Clinical Study Coordinators

Campus, IL · On-site

$22K - $51K/mo

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

Clinical Study Coordinators

Campus, IL · On-site

$22K - $51K/mo

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

Job Scope The Clinical Study Coordinator plays an integral role in supporting the conduct of ... Day-to-day "hands on" work associated with in-house clinical studies * Coordinate execution of site ...

Job Scope The Clinical Study Coordinator plays an integral role in supporting the conduct of ... Day-to-day "hands on" work associated with in-house clinical studies * Coordinate execution of site ...

$90 - $130/hr

Serve as a clinical and technical resource for site coordinators, investigators, field clinical ... Collaborate with study teams, field personnel, and investigative sites to resolve data ...

New

next page

Showing results 1-20

Clinical Studies Coordinator information

See salary details

$11

$28

$46

How much do clinical studies coordinator jobs pay per hour?

As of Sep 3, 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 is a clinical studies coordinator?

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 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 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.

What does a clinical studies coordinator do?

A clinical studies coordinator manages and oversees the daily operations of clinical trials, ensuring protocols are followed, data is accurately collected, and regulatory requirements are met. They coordinate between research teams, participants, and regulatory bodies, often using electronic data capture systems, and typically need knowledge of Good Clinical Practice (GCP) guidelines. The role requires strong organizational skills and attention to detail to support the successful completion of clinical research studies.
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:

Infographic showing various Clinical Studies Coordinator job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $59,597 per year, or $28.7 per hour.

Clinical Studies Coordinator I -Translational Neuroscience

Advocate Aurora Health

Winston Salem, NC • On-site

$24.10 - $36.15/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago


Advocate Aurora Health rating

7.6

Company rating: 7.6 out of 10

Based on 781 frontline employees who took The Breakroom Quiz

192nd of 898 rated healthcare providers


Job description

Department:

85046 Wake Forest University Health Sciences - Academic Translational Neuroscience

Status:

Full time

Benefits Eligible:

Yes

Hours Per Week:

40

Schedule Details/Additional Information:

8.5-hour Shift between 8 am-5:30 pm (30-minute lunch break), sometimes required to work later M-F or on weekends to accommodate human subjects availability to participate in the study.

Must have valid NC driver's license, reliable transportation

Pay Range:

$24.10 - $36.15

******Grant-funded Position******

JOB SUMMARY

Under general supervision, responsible for the compilation and collection of data, recruitment of subjects, and general coordination of clinical studies. Participate in the implementation of multiple NIH-funded clinical research studies that investigate how substance use affects people who have or are at risk for HIV in North Carolina. The study coordinator will work in a team which uses multimodal data collection, including clinical interviews, neuropsychological testing, blood draws and urine screens, MRI brain scans, and medical record abstractions. Responsibilities of the coordinator include: recruitment, enrollment, and tracking of participants; visit scheduling; data collection; data management and quality assurance; regulatory duties; supervision of auxiliary staff; and other relevant administrative tasks. The coordinator will be work closely with study investigators to track progress and implement protocols.

EDUCATION/EXPERIENCE

Bachelor's degree in a related field of study or an equivalent combination of experience and education.

Experience in a medical and/or research setting.

Paramedical or other clinical experience.

LICENSURE, CERTIFICATION, and/or REGISTRATION

Registered Record Administrator preferred.

ESSENTIAL FUNCTIONS

1. Assists principal investigator and other health professionals in troubleshooting various problems related to the management of the clinical study. Assists in all aspects of the data collection process.

2. Performs technical procedures on clinical subjects under the direction of the principal investigator or his/her designee.

3. Assists with recruitment of patients for the clinical study including tracking the sources of patient referrals. Follow-up with sources of patient referrals including referring doctors, various Medical Center labs, and other sources.

4. Maintains appropriate patient records as necessary. This includes charting the condition of the patient and determining their continued eligibility in the study.

5. Obtains and interprets pertinent data from medical records as needed to understand past and present condition of the patients.

6. Performs day-to-day administrative and clerical duties such as designing brochures, stationery and data forms. Creates reports and graphs pertinent to the study including presentation of the results of the study.

7. May supervise other personnel including volunteers as assigned.

8. Assists in development of suitable codes and data collection forms for computerization.

9. Consults and cooperates with all faculty, coordination centers, sponsors, and health professionals involved in the clinical study.

10. Performs other related duties incidental to the work described herein.

SKILLS/QUALIFICATIONS

Understanding of medical and/or scientific terminology

Strong oral, written, and interpersonal communication skills

WORK ENVIRONMENT

Clean, well-lit, office environment

Our CommitmenttoYou:

Advocate Health offers a comprehensive suite of Total Rewards: benefits and well-being programs, competitive compensation, generous retirement offerings, programs that invest in your career development and so much more - so you can live fully at and away from work, including:

Compensation

  • Base compensation listed within the listed pay range based on factors such as qualifications, skills, relevant experience, and/or training

  • Premium pay such as shift, on call, and more based on a teammate's job

  • Incentive pay for select positions

  • Opportunity for annual increases based on performance

Benefits and more

  • Paid Time Off programs

  • Health and welfare benefits such as medical, dental, vision, life, andShort- and Long-Term Disability

  • Flexible Spending Accounts for eligible health care and dependent care expenses

  • Family benefits such as adoption assistance and paid parental leave

  • Defined contribution retirement plans with employer match and other financial wellness programs

  • Educational Assistance Program

Note: Eligibility for programs listed above may depend on your FTE or status (e.g., full-time, part-time, per diem, temporary, etc.); please ask a Recruiter for more information during an interview.


About Advocate Health

Advocate Health is the third-largest nonprofit, integrated health system in the United States, created from the combination of Advocate Aurora Health and Atrium Health. Providing care under the names Advocate Health Care in Illinois; Atrium Health in the Carolinas, Georgia and Alabama; and Aurora Health Care in Wisconsin, Advocate Health is a national leader in clinical innovation, health outcomes, consumer experience and value-based care. Headquartered in Charlotte, North Carolina, Advocate Health services nearly 6 million patients and is engaged in hundreds of clinical trials and research studies, with Wake Forest University School of Medicine serving as the academic core of the enterprise. It is nationally recognized for its expertise in cardiology, neurosciences, oncology, pediatrics and rehabilitation, as well as organ transplants, burn treatments and specialized musculoskeletal programs. Advocate Health employs 155,000 teammates across 69 hospitals and over 1,000 care locations, and offers one of the nation's largest graduate medical education programs with over 2,000 residents and fellows across more than 200 programs. Committed to providing equitable care for all, Advocate Health provides more than $6 billion in annual community benefits.


What Advocate Aurora Health employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


Advocate Health logo

About Advocate Health

Sourced by ZipRecruiter

Advocate Healthcare, based in Oak Lawn, Illinois, United States, is a leading figure in the health care industry. Accessible via their official website, 'advocatehealth.com', this organization provides a wide variety of medical services and treatment options. Founded in 1995 through a merger of Evangelical Health Systems Corporation and Lutheran General HealthSystem, Advocate Healthcare has grown exponentially over the years. Now, it operates more than 400 sites of care, including 12 hospitals that encompass 11 acute care hospitals, the state’s largest integrated children’s network, five Level I trauma centers, and three Level II trauma centers. Upholding their values of equality, compassion, excellence, partnership and stewardship, Advocate Healthcare's mission is centered on building lifelong relationships with patients by delivering the best health outcomes and highest level of service through an integrated approach to care and wellness.

Industry

Hospitals and health care and social assistance

Company size

10,000+ Employees

Headquarters location

Charlotte, NC, US