What does a clinical coordinator do? Three jobs, one title
"Clinical coordinator" can mean a research coordinator running trial visits, a nurse coordinating a unit or program, or a school's clinical placement lead, and candidates rarely cross between them. Careerscape's healthcare recruiters work remotely nationwide and start every coordinator search by pinning down which of the three you need.
Research, care delivery or education: defined first
GCP training and CCRC/CCRP status checked
Direct hire or contract coordinators
Definitions
The three jobs called clinical coordinator
Write the setting into the title. O*NET lists "Clinical Coordinator" as a reported title for clinical research coordinators, but hospitals and schools use the same words for different work.
Clinical research (trial sites, academic medical centers, CROs)
Clinical research coordinator
Clinical trial coordinator
Research nurse coordinator
Regulatory coordinator
Lead CRC / research manager
Care delivery (hospitals, clinics, post-acute)
Unit or department coordinator
Transplant coordinator
Oncology or cardiac program coordinator
Care transitions coordinator
Quality and accreditation coordinator
Education (nursing and allied health programs)
Clinical placement coordinator
Director of clinical education
Clinical site liaison
Preceptor program coordinator
Template
Clinical research coordinator job description
Research coordination is the most common meaning in searches and on job boards, so this template covers it. The duties follow O*NET's task list for clinical research coordinators. For a care delivery coordinator, swap the trial duties for scheduling, staffing and quality work.
We are hiring a clinical research coordinator to run day-to-day study activity for our investigators: screening and enrolling participants, completing protocol visits, keeping regulatory files audit-ready and reporting data on time.
Responsibilities
Screen potential participants through interviews, record review and discussion with physicians and nurses
Obtain and document informed consent and oversee enrollment
Schedule and complete protocol visits, including vital signs, ECGs and specimen collection as trained
Record adverse events and work with investigators on reporting to sponsors and the IRB
Keep case report forms, drug accountability logs and regulatory binders current
Prepare IRB submissions, amendments, deviation reports and progress reports
Spot protocol problems early and help investigators resolve them
Host sponsor monitoring visits and close out queries
Requirements
Bachelor's degree in a health or science field, or equivalent research experience
Current Good Clinical Practice (GCP) training
Working knowledge of FDA regulations, IRB processes and informed consent
Experience with a clinical trial management system or EDC platform
Careful documentation habits and comfort talking with patients about studies
Nice to have
CCRC (ACRP) or CCRP (SOCRA) certification
Therapeutic area experience matching your portfolio, such as oncology or cardiology
Phlebotomy or RN licensure for visits with clinical procedures
Experience with ICH E6(R3) risk-based monitoring and validated electronic systems
Credential path
How a research coordinator builds credentials
These are credentials, not licenses. They are the markers research sites screen for, in the order most coordinators earn them.
01
GCP training
Under NIH policy effective January 1, 2017, investigators and staff on NIH-funded clinical trials, including those handling coordination and data, should be trained in Good Clinical Practice and refresh that training at least every three years.
02
Paid research experience
Both major certifications require documented work on human-subject research. Internships and degree coursework do not count toward ACRP's hours.
03
CCRC from ACRP
ACRP's Certified Clinical Research Coordinator exam requires 3,000 hours of verifiable, paid clinical research work, with a possible one-time 1,500-hour waiver for approved education. The exam has 125 questions in 180 minutes, and certification is valid for two years.
04
Or CCRP from SOCRA
SOCRA's Certified Clinical Research Professional has three eligibility categories. A degree in clinical research, or a clinical research certificate plus a science or health degree, qualifies with one year of full-time experience in the past two years; SOCRA says most candidates qualify under its first, experience-based category.
05
Keep up with E6(R3)
FDA published the final ICH E6(R3) GCP guideline in the Federal Register on September 9, 2025, without a formal U.S. compliance date. It stresses quality by design, risk-based oversight and validated systems, so ask how a candidate's site has adapted.
Interview
Five questions for a coordinator candidate
Ask for real examples. Strong coordinators describe documents, systems and people by name.
Q1
Walk me through how you consent a participant, from first contact to the signed form in the file.
Listen for: Correct version control, time for questions, a plan for patients with limited English or capacity concerns, and documentation of the process, not just the signature.
Q2
Tell me about a protocol deviation you caught. What happened next?
Listen for: Ownership, prompt reporting to the PI and IRB as required, and a fix to the process so it does not repeat.
Q3
How many active studies have you carried at once, and in which phases?
Listen for: A number that matches the complexity of your portfolio. Phase I oncology work is far more demanding per study than an observational registry.
Q4
Which CTMS, EDC or eConsent systems have you used?
Listen for: Named systems and how quickly they learned a new sponsor's platform. O*NET lists clinical trial management software among the core tools.
Q5
How do you prepare for a monitoring visit?
Listen for: A routine for reconciling source documents, logs and queries ahead of time, and a calm working relationship with monitors.
Approximate pay
BLS pay figures for this title need a caveat
BLS counts clinical coordinators and other clinical operations leads with medical and health services managers, so the national figures below cover a broader and more senior group than most coordinator roles. See our healthcare administrator salary guide for that group.
$73,39010th
$94,70025th
$123,860Median
$166,10075th
$224,34090th
Middle half of all workers (25th to 75th percentile)
Read the lower end of the range for coordinators. The 10th to 25th percentile ($73,390 to $94,700) is closer to a lead coordinator or program coordinator with supervisory duties. The median ($123,860) and above reflect directors and executives. O*NET classifies clinical research coordinators separately, under natural sciences managers, which is another sign that the manager figures overstate typical research coordinator pay. Annual pay, all U.S. employers, BLS Occupational Employment and Wage Statistics (May 2025), occupation: Medical and Health Services Managers. BLS does not publish this title separately; the figures are for medical and health services managers, the closest BLS occupation, which can include other job titles. Closest Salary Guide page: Healthcare Administrator.
29 metros
Where clinical operations jobs cluster
These are BLS metro numbers (May 2025) for the broader SOC 11-9111 manager occupation. Treat these as a guide to where clinical operations work is concentrated, not as coordinator pay. Our healthcare staffing pages describe each market.
Baltimore (1.55), Providence (1.51) and Pittsburgh (1.40) have the highest concentrations, followed by San Francisco (1.31) and Nashville (1.30). Academic medical centers and research hospitals in metros like these tend to post many research coordinator jobs. Boston (1.25) and Philadelphia (1.26) are also above average. Seattle and Atlanta (both 0.57) are the thinnest. Pittsburgh's median ($101,570) is the lowest on the table, while New York City ($167,580) and San Francisco ($166,310) are the highest. Medical and Health Services Managers, by metro area, sorted by jobs. BLS Occupational Employment and Wage Statistics, May 2025; U.S. median $123,860. Concentration is the BLS location quotient: above 1.0 means the job is a bigger share of local employment than nationally.
Tell us which kind of coordinator you need (research, care delivery or education), the setting, any license or certification required, and the hiring model you prefer.
A short list of screened candidates, not a stack of resumes
Direct hire, contract, contract-to-hire or executive search
Review candidates and give feedback in your Employer Portal
It depends on the setting. In research, a clinical coordinator screens and enrolls study participants, obtains informed consent, runs protocol visits and keeps regulatory records. In a hospital or clinic, the title usually means coordinating a unit or specialty program: scheduling, staffing, quality and patient flow. In nursing and allied health schools, it means arranging and overseeing students' clinical placements. Job postings should say which one.
Does a clinical research coordinator need certification?
No license or certification is legally required, but many sites prefer ACRP's CCRC or SOCRA's CCRP. NIH-funded trials expect investigators and coordination staff to complete Good Clinical Practice training and refresh it at least every three years. For newer coordinators, current GCP training plus documented research experience is the realistic bar; certification usually follows a year or two of paid work.
Should a clinical coordinator be a nurse?
Only if the job needs nursing judgment or procedures. Many research coordinators are not nurses. Unit and transplant coordinators in hospitals often are RNs, because they triage, educate patients and work under nursing protocols. If the role involves assessments or medication administration, require an RN license; if it is mostly scheduling, documentation and regulatory work, a non-nurse coordinator is usually a better match.
Can we hire clinical research coordinators on contract?
Yes. Sites use contract staffing to cover a study start-up, a leave or a spike in enrollment, and contract-to-hire to test fit with investigators. For a long-term portfolio, direct hire keeps knowledge of your studies in-house. Careerscape's recruiters check GCP training dates and certification status before you see a candidate.
I want to become a clinical research coordinator. Where do I start?
Entry roles such as research assistant or study assistant at a site often lead to coordinator jobs. Complete GCP training, then build paid research hours toward ACRP's or SOCRA's certification. Careerscape's job seeker services are free and confidential; browse open jobs or submit your resume.
Not sure which coordinator you need?
Describe the work and a healthcare recruiter will help you title and scope the role before the search starts. That one step avoids most mismatched applicants.