We are currently seeking an Epic Clinical Subject Matter Expert& Project Manager to join our Health ... Identifyopportunities to improve documentation quality, care coordination, patient access to care ...
We are currently seeking an Epic Clinical Subject Matter Expert& Project Manager to join our Health ... Identifyopportunities to improve documentation quality, care coordination, patient access to care ...
The Clinical Research Data Coordinator I supports the research program within the Clinical Trials ... Attends study team meetings and provides updates to study team members regarding protocol data ...
The Clinical Research Data Coordinator I supports the research program within the Clinical Trials ... Attends study team meetings and provides updates to study team members regarding protocol data ...
The Clinical Research Data Coordinator I supports the research program within the Clinical Trials ... Attends study team meetings and provides updates to study team members regarding protocol data ...
The Clinical Research Data Coordinator I supports the research program within the Clinical Trials ... Attends study team meetings and provides updates to study team members regarding protocol data ...
The Clinical Research Data Coordinator I supports the research program within the Clinical Trials ... Attends study team meetings and provides updates to study team members regarding protocol data ...
The Clinical Research Data Coordinator I supports the research program within the Clinical Trials ... Attends study team meetings and provides updates to study team members regarding protocol data ...
We are currently seeking an Epic Clinical Subject Matter Expert & Project Manager to join our ... Identify opportunities to improve documentation quality, care coordination, patient access to care ...
We are currently seeking an Epic Clinical Subject Matter Expert & Project Manager to join our ... Identify opportunities to improve documentation quality, care coordination, patient access to care ...
We are currently seeking an Epic Clinical Subject Matter Expert & Project Manager to join our ... Identify opportunities to improve documentation quality, care coordination, patient access to care ...
We are currently seeking an Epic Clinical Subject Matter Expert & Project Manager to join our ... Identify opportunities to improve documentation quality, care coordination, patient access to care ...
Experience in creating and negotiating study budgets * Experience in financial management ... Clinical Research Coordinator (CCRC), or comparable within 1 year of employment * ARUP Handling ...
Experience in creating and negotiating study budgets * Experience in financial management ... Clinical Research Coordinator (CCRC), or comparable within 1 year of employment * ARUP Handling ...
Clinical Research Coordinator - Marietta, GA Work Set-Up: On-site Schedule Weekly Hours: 24 hours ... Coordinate clinical research studies and maintain compliance with protocols and Good Clinical ...
Clinical Research Coordinator - Marietta, GA Work Set-Up: On-site Schedule Weekly Hours: 24 hours ... Coordinate clinical research studies and maintain compliance with protocols and Good Clinical ...
Clinical Research Coordinator - Marietta, GA
Marietta, GA · On-site
$35 - $42/hr
Clinical Research Coordinator - Marietta, GA Work Set-Up: On-site Schedule Weekly Hours: 24 hours ... Coordinate clinical research studies and maintain compliance with protocols and Good Clinical ...
Clinical Research Coordinator - Marietta, GA
Marietta, GA · On-site
$35 - $42/hr
Clinical Research Coordinator - Marietta, GA Work Set-Up: On-site Schedule Weekly Hours: 24 hours ... Coordinate clinical research studies and maintain compliance with protocols and Good Clinical ...
Facilitates study monitoring visits and prompt resolution of all study related queries. KEY RESPONSIBILITIES: * Primary Data Coordinator (DC) for complex interventional therapeutic clinical trials ...
Facilitates study monitoring visits and prompt resolution of all study related queries. KEY RESPONSIBILITIES: * Primary Data Coordinator (DC) for complex interventional therapeutic clinical trials ...
Facilitates study monitoring visits and prompt resolution of all study related queries. KEY RESPONSIBILITIES: * Primary Data Coordinator (DC) for complex interventional therapeutic clinical trials ...
Facilitates study monitoring visits and prompt resolution of all study related queries. KEY RESPONSIBILITIES: * Primary Data Coordinator (DC) for complex interventional therapeutic clinical trials ...
Facilitates study monitoring visits and prompt resolution of all study related queries. KEY RESPONSIBILITIES: * Primary Data Coordinator (DC) for complex interventional therapeutic clinical trials ...
Facilitates study monitoring visits and prompt resolution of all study related queries. KEY RESPONSIBILITIES: * Primary Data Coordinator (DC) for complex interventional therapeutic clinical trials ...
Clinical Research Assistant
Decatur, GA · On-site
Clinical Research Assistant Department: Operations Employment Type: Full Time Location: Accel ... Ensures study related reports and patient results are reviewed by the Research Coordinator and/or ...
Clinical Research Assistant
Decatur, GA · On-site
Clinical Research Assistant Department: Operations Employment Type: Full Time Location: Accel ... Ensures study related reports and patient results are reviewed by the Research Coordinator and/or ...
Clinical Research Coordinator II - School of Medicine Neurology
Atlanta, GA · On-site
$23.75 - $31.75/hr
Description The Clinical Research Coordinator II handles administrative activities generally ... The coordinator will oversee the day-to-day operations of the study, including participant ...
Clinical Research Coordinator II - School of Medicine Neurology
Atlanta, GA · On-site
$23.75 - $31.75/hr
Description The Clinical Research Coordinator II handles administrative activities generally ... The coordinator will oversee the day-to-day operations of the study, including participant ...
The Clinical Research Coordinator II handles administrative activities generally associated with ... The coordinator will oversee the day-to-day operations of the study, including participant ...
The Clinical Research Coordinator II handles administrative activities generally associated with ... The coordinator will oversee the day-to-day operations of the study, including participant ...
Senior Clinical Supervisor
Atlanta, GA · On-site
Program Operations * Assist with oversight of program functioning, including scheduling, coverage, and service coordination. * Facilitate team clinical leadership meetings to support collaboration ...
Senior Clinical Supervisor
Atlanta, GA · On-site
Program Operations * Assist with oversight of program functioning, including scheduling, coverage, and service coordination. * Facilitate team clinical leadership meetings to support collaboration ...
Ensures study related reports and patient results are reviewed by the Research Coordinator and/or ... A High School diploma and 1 year of administrative / clinical experience is required. 1 year or ...
Quick apply
Ensures study related reports and patient results are reviewed by the Research Coordinator and/or ... A High School diploma and 1 year of administrative / clinical experience is required. 1 year or ...
Description The Clinical Research Coordinator II handles administrative activities generally ... The coordinator will oversee the day-to-day operations of the study, including participant ...
Description The Clinical Research Coordinator II handles administrative activities generally ... The coordinator will oversee the day-to-day operations of the study, including participant ...
Part-Time Re-Entry Clinical Coordinator
Atlanta, GA · On-site
$40/hr
Job Title: Part-Time Re-Entry Clinical Coordinator Job Requisition ID: JR0000001325 Number of ... Identify and secure Georgia Board of Nursing-approved clinical preceptors for the Clinical Study ...
Part-Time Re-Entry Clinical Coordinator
Atlanta, GA · On-site
$40/hr
Job Title: Part-Time Re-Entry Clinical Coordinator Job Requisition ID: JR0000001325 Number of ... Identify and secure Georgia Board of Nursing-approved clinical preceptors for the Clinical Study ...
Medical Science Liaison
Atlanta, GA · On-site
$190 - $210/hr
... study coordinators, and other healthcare professionals while developing a strong understanding of clinical practice and evolving therapeutic landscapes. * Partner with Clinical Development, Clinical ...
Medical Science Liaison
Atlanta, GA · On-site
$190 - $210/hr
... study coordinators, and other healthcare professionals while developing a strong understanding of clinical practice and evolving therapeutic landscapes. * Partner with Clinical Development, Clinical ...
Clinical Study Coordinator information
See Decatur, GA salary details
$27.3K - $35.1K
3% of jobs
$35.1K - $43K
7% of jobs
$43K - $50.8K
11% of jobs
$51.9K is the 25th percentile. Wages below this are outliers.
$50.8K - $58.6K
26% of jobs
The median wage is $59.8K / yr.
$58.6K - $66.4K
21% of jobs
$72.7K is the 75th percentile. Wages above this are outliers.
$66.4K - $74.2K
9% of jobs
$74.2K - $82K
10% of jobs
$82K - $89.8K
6% of jobs
$89.8K - $97.6K
6% of jobs
$97.6K - $105.4K
1% of jobs
$105.4K - $113.3K
0% of jobs
$27.3K
$65.9K
$113.3K
How much do clinical study coordinator jobs pay per year?
What is the difference between Clinical Study Coordinator vs Clinical Research Associate?
| Aspect | Clinical Study Coordinator | Clinical Research Associate |
|---|---|---|
| Required Credentials | Typically a bachelor's degree in health sciences or related field; certifications like CCRP are a plus | Often a bachelor's degree in life sciences; certifications like CCRP or RAC are common |
| Work Environment | Conducts site visits, manages study activities at clinical sites | Monitors multiple sites remotely or on-site, ensuring protocol compliance |
| Employer & Industry Usage | Hospitals, clinics, research sites | Pharmaceutical 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?
What are the key skills and qualifications needed to thrive as a clinical study coordinator?

Job description
We are the leading provider of professional services to the middle market globally, our purpose is to instill confidence in a world of change, empowering our clients and people to realize their full potential. Our exceptional people are the key to our unrivaled, culture and talent experience and our ability to be compelling to our clients. You'll find an environment that inspires and empowers you to thrive both personally and professionally. There's no one like you and that's why there's nowhere like RSM.
We are currently seeking an Epic Clinical Subject Matter Expert& Project Manager to join our Healthcare Technology Consulting Services team. The Senior Associate willoperateacross multiple Epic engagements and willbe responsible forsupporting high-quality delivery across clinical implementations, optimization initiatives, stabilization efforts, and transformation programs.
The Senior Associate willleveragestrong Epic clinical applicationexpertise, healthcare operational knowledge, and project management discipline to help clients improve care delivery, provider workflows, patient safety, and operational efficiency. This role requires an experienced professional who can balance hands-on Epic consulting work with project coordination, stakeholder management, and internal practice support.
The successful candidate will havedemonstratedexperience supporting Epic clinical projects or major workstreams, solving client challenges, organizing complex initiatives, and contributing to successful delivery outcomes. This role includes active participation in client engagements, project governance, delivery execution, andpracticegrowth initiatives.
*This role offers flexibility to be based near any major RSM office
As a Healthcare Consulting Senior Associate, you will need to:
Perform hands-on Epic clinical delivery work across implementations, optimizations, upgrades, and stabilization engagements while serving as an Epic subject matter expert or workstream lead on client engagements as needed.
Support clinical workflow design, build validation, testing, go-live readiness, post-go-live support, and command center operations during critical milestones.
Analyze current-state clinical workflows andidentifyopportunities to improve provider efficiency, nursing workflows, patient safety, documentation quality, throughput, and user adoption.
Ensure solutions align with EpicSystemsbest practices, regulatory expectations, and long-term sustainability.
Support optimization of provider documentation tools, order sets, preference lists, in-basket workflows, clinical decision support, and patient care coordination tools.
Develop and manage project plans, timelines, dependencies, RAID logs, meeting cadences, status reporting, and overall project execution discipline.
Coordinate cross-functional teams including physicians, nursing, ancillary departments, IT, training, testing, informatics, and third-party vendors while driving accountability across stakeholders.
Facilitate working sessions, steering committees, governance meetings, executive updates, andactivationreadiness planning.
Helpmaintaindelivery quality, scope control, timeline adherence, and proactiveissueescalation throughout engagements.
Support optimization assessments across Epic clinical workflows, governance models, provider adoption, and operational performance.
Identifyopportunities to improve documentation quality, care coordination, patient access to care, throughput, patient satisfaction, and clinical productivity.
Translate client pain points into actionable Epic enhancement strategies, future-state workflow designs, and prioritized improvement roadmaps.
Support proposal development, RFP responses, scopes of work, client presentations, staffing plans, and effort estimates.
Help create andmaintaindeliverytemplates, tools, standards, methodologies, and reusable practice assets.
Mentor associates and junior team members whileparticipatingin interviewing, onboarding, and coaching Epic consultants.
Contribute to practice growth through strong delivery outcomes, trusted client relationships, and identification of expansion opportunities.
Professional Qualifications:
Bachelor's degree in a related field or equivalent professional experience.
Active Epic certification in at least one clinical Epic application isrequired.
4+ years of hands-on Epic clinical implementation, optimization, support, or healthcare operations experience.
Demonstrated experience supporting Epic clinical projects, implementations, or major workstreams.
Strong understanding of ambulatory,inpatient, emergency, perioperative, or ancillary clinical workflows.
Experience managing project plans, risks, timelines, and stakeholder expectations.
Proven ability to support multiple concurrent engagements.
Strong written and verbal communication skills.
Strong interpersonal skills and ability to work directly with physicians, nurses, operational leaders, and client stakeholders.
Ability to balance billable delivery responsibilities with internal leadership contributions.
Willingness and ability to travel as needed for client engagements (25%-75%).
Preferred Qualifications:
Multiple certifications such as Epic Systems Ambulatory, Inpatient Clinical Documentation, Orders, ASAP, Stork, Willow, Cupid, OpTime, Anesthesia, or Healthy Planet, Radiant
Former Epic Systems experience.
Clinical background as RN, NP, PA, therapist, pharmacist, orotherlicensed caregiver.
Experience serving as a project manager, PMO lead, or Epic workstream lead.
Experience supporting go-lives and post-go-live stabilization.
Experience mentoring junior consulting staff.
Experience contributing to proposals, RFPs, or practice development efforts.
Experience working in a high-growth or evolving consulting practice.
At RSM, we offer a competitive benefits and compensation package for all our people.We offer flexibility in your schedule, empowering you to balance life's demands, while also maintaining your ability to serve clients.Learn more about our total rewards at https://rsmus.com/careers/working-at-rsm/benefits.
All applicants will receive consideration for employment as RSM does not tolerate discrimination and/or harassment based on race; color; creed; sincerely held religious beliefs, practices or observances; sex (including pregnancy or disabilities related to nursing); gender; sexual orientation; HIV Status; national origin; ancestry; familial or marital status; age; physical or mental disability; citizenship; political affiliation; medical condition (including family and medical leave); domestic violence victim status; past, current or prospective service in the US uniformed service; US Military/Veteran status; pre-disposing genetic characteristics or any other characteristic protected under applicable federal, state or local law.
Accommodation for applicants with disabilities is available upon request in connection with the recruitment process and/or employment/partnership.RSM is committed to providing equal opportunity and reasonable accommodation for people with disabilities. If you require a reasonable accommodation to complete an application, interview, or otherwise participate in the recruiting process, please call us at 800-274-3978 or send us an email at careers@rsmus.com.
RSM does not intend to hire entry level candidates who will require sponsorship now OR in the future (i.e. F-1 visa holders). If you are a recent U.S. college / university graduate possessing 1-2 years of progressive and relevant work experience in a same or similar role to the one for which you are applying, excluding internships, you may be eligible for hire as an experienced associate.
RSM will consider for employment qualified applicants with arrest or conviction records. For those living in California or applying to a position in California, please click here for additional information.
At RSM, an employee's pay at any point in their career is intended to reflect their experiences, performance, and skills for their current role. The salary range (or starting rate for interns and associates) for this role represents numerous factors considered in the hiring decisions including, but not limited to, education, skills, work experience, certifications, location, etc. As such, pay for the successful candidate(s) could fall anywhere within the stated range.
Compensation Range: $85,100 - $161,700Individualsselected for this role will be eligible for a discretionary bonus based on firm and individual performance.