The Senior Associate will leverage strong Epic clinical application expertise, healthcare operational knowledge, and project management discipline to help clients improve care delivery, provider ...
The Senior Associate will leverage strong Epic clinical application expertise, healthcare operational knowledge, and project management discipline to help clients improve care delivery, provider ...
The Senior Associate will leverage strong Epic clinical application expertise, healthcare operational knowledge, and project management discipline to help clients improve care delivery, provider ...
The Senior Associate will leverage strong Epic clinical application expertise, healthcare operational knowledge, and project management discipline to help clients improve care delivery, provider ...
Associate Study Coordinator- ISR & Biocompatibility
Minneapolis, MN · On-site
$24/hr
Assists Study Directors on select projects under the direction and review of the Study Director ... Assists in collection, documentation and analysis of pre-clinical data. Assists in the coordination ...
New
Associate Study Coordinator- ISR & Biocompatibility
Minneapolis, MN · On-site
$24/hr
Assists Study Directors on select projects under the direction and review of the Study Director ... Assists in collection, documentation and analysis of pre-clinical data. Assists in the coordination ...
New
The Senior Associate will leverage strong Epic clinical application expertise, healthcare operational knowledge, and project management discipline to help clients improve care delivery, provider ...
The Senior Associate will leverage strong Epic clinical application expertise, healthcare operational knowledge, and project management discipline to help clients improve care delivery, provider ...
Principal Clinical Scientist
Chaska, MN · On-site +1
Our associates are involved in every stage of diagnostics, from ideation to development and ... You will drive strategic study designs, ensuring regulatory compliance, and achieving key ...
Principal Clinical Scientist
Chaska, MN · On-site +1
Our associates are involved in every stage of diagnostics, from ideation to development and ... You will drive strategic study designs, ensuring regulatory compliance, and achieving key ...
Principal Clinical Scientist
Chaska, MN · On-site
$120K - $165K/yr
Our associates are involved in every stage of diagnostics, from ideation to development and ... You will drive strategic study designs, ensuring regulatory compliance, and achieving key ...
Principal Clinical Scientist
Chaska, MN · On-site
$120K - $165K/yr
Our associates are involved in every stage of diagnostics, from ideation to development and ... You will drive strategic study designs, ensuring regulatory compliance, and achieving key ...
May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and ...
May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and ...
Senior Clinical Research Associate
Minneapolis, MN · On-site +1
$90K - $120K/yr
Centralized Monitoring: • Leads and trains others in reviewing study site data and data reports ... Other duties as required for clinical operations: • Performs all duties in compliance with ...
Senior Clinical Research Associate
Minneapolis, MN · On-site +1
$90K - $120K/yr
Centralized Monitoring: • Leads and trains others in reviewing study site data and data reports ... Other duties as required for clinical operations: • Performs all duties in compliance with ...
MDR - Sr Prin Clinical Research Spec - Exempt
Moundsview, MN · On-site
$60 - $65/hr
Oversee, design, plan, and develop clinical evaluation research studies. * Prepare and author protocols and patient record forms. * Conduct registered and nonregistered clinical studies of products ...
MDR - Sr Prin Clinical Research Spec - Exempt
Moundsview, MN · On-site
$60 - $65/hr
Oversee, design, plan, and develop clinical evaluation research studies. * Prepare and author protocols and patient record forms. * Conduct registered and nonregistered clinical studies of products ...
Clinical and Research Post-Doctoral Associate - Raptor and Wildlife Health
Minneapolis, MN · On-site
$62K - $65K/mo
... Clinical and Research Post-Doctoral Associate is a unique position that offers a balanced 50/50 ... Develop studies focusing on current wildlife health priorities, potentially including but not ...
Clinical and Research Post-Doctoral Associate - Raptor and Wildlife Health
Minneapolis, MN · On-site
$62K - $65K/mo
... Clinical and Research Post-Doctoral Associate is a unique position that offers a balanced 50/50 ... Develop studies focusing on current wildlife health priorities, potentially including but not ...
Participate in development of safety-related data collection forms for clinical studies ... Associate's degree and 10 years of related experience OR High school diploma / GED and 12 years of ...
Participate in development of safety-related data collection forms for clinical studies ... Associate's degree and 10 years of related experience OR High school diploma / GED and 12 years of ...
CRC I
Minneapolis, MN · On-site
$24 - $32/hr
They ensure smooth, accurate progress of clinical studies in accordance with all legal and ... Associate or Bachelor's degree. * A minimum of one year of clinical experience. * Proficiency in MS ...
Quick apply
CRC I
Minneapolis, MN · On-site
$24 - $32/hr
They ensure smooth, accurate progress of clinical studies in accordance with all legal and ... Associate or Bachelor's degree. * A minimum of one year of clinical experience. * Proficiency in MS ...
Associate Clinical Research Coordinator - Alzheimer's Disease Research - Limited Tenure
Rochester, MN · On-site
$24.55 - $35.65/hr
May assist in complex (i.e. interventional, therapeutic, greater than minimal risk) studies with ... Associate's in Clinical Research from an accredited academic institution without experience OR
Associate Clinical Research Coordinator - Alzheimer's Disease Research - Limited Tenure
Rochester, MN · On-site
$24.55 - $35.65/hr
May assist in complex (i.e. interventional, therapeutic, greater than minimal risk) studies with ... Associate's in Clinical Research from an accredited academic institution without experience OR
Clinical Research Associate (CRA) II
Brooklyn Park, MN · On-site +1
The Role The Clinical Research Associate (CRA) II performs the day-to-day operations associated ... Becomes proficient with all study databases, systems and company quality management system
Clinical Research Associate (CRA) II
Brooklyn Park, MN · On-site +1
The Role The Clinical Research Associate (CRA) II performs the day-to-day operations associated ... Becomes proficient with all study databases, systems and company quality management system
Oncodea is seeking a passionate and driven Molecular Diagnostic Associate to join our team and help ... Support clinical study execution and CLIA-LDT lab setup, including sample kitting, shipment, and ...
Quick apply
Oncodea is seeking a passionate and driven Molecular Diagnostic Associate to join our team and help ... Support clinical study execution and CLIA-LDT lab setup, including sample kitting, shipment, and ...
Associate Clinical Research Coordinator - Alzheimer's Disease Research - Limited Tenure
Rochester, MN · On-site
$24.75 - $32.75/hr
May assist in complex (i.e. interventional, therapeutic, greater than minimal risk) studies with ... Associate's in Clinical Research from an accredited academic institution without experience OR
Associate Clinical Research Coordinator - Alzheimer's Disease Research - Limited Tenure
Rochester, MN · On-site
$24.75 - $32.75/hr
May assist in complex (i.e. interventional, therapeutic, greater than minimal risk) studies with ... Associate's in Clinical Research from an accredited academic institution without experience OR
Associate Clinical Research Coordinator - Alzheimer's Disease Research - Limited Tenure
Rochester, MN · On-site
$23.75 - $31.50/hr
May assist in complex (i.e. interventional, therapeutic, greater than minimal risk) studies with ... Associate's in Clinical Research from an accredited academic institution without experience OR
Associate Clinical Research Coordinator - Alzheimer's Disease Research - Limited Tenure
Rochester, MN · On-site
$23.75 - $31.50/hr
May assist in complex (i.e. interventional, therapeutic, greater than minimal risk) studies with ... Associate's in Clinical Research from an accredited academic institution without experience OR
Associate Clinical Research Coordinator - Alzheimer's Disease Research - Limited Tenure
Rochester, MN · On-site
$23.75 - $31.50/hr
May assist in complex (i.e. interventional, therapeutic, greater than minimal risk) studies with ... Associate's in Clinical Research from an accredited academic institution without experience OR
Associate Clinical Research Coordinator - Alzheimer's Disease Research - Limited Tenure
Rochester, MN · On-site
$23.75 - $31.50/hr
May assist in complex (i.e. interventional, therapeutic, greater than minimal risk) studies with ... Associate's in Clinical Research from an accredited academic institution without experience OR
Clinical & Regulatory Affairs
Minneapolis, MN · On-site
Clinical Research Associate * Clinical Research Scientist * Clinical Specialist * Regulatory ... or global clinical studies are especially encouraged to apply. Successful candidates are ...
Quick apply
Clinical & Regulatory Affairs
Minneapolis, MN · On-site
Clinical Research Associate * Clinical Research Scientist * Clinical Specialist * Regulatory ... or global clinical studies are especially encouraged to apply. Successful candidates are ...
The study load and complexity will increase from the Associate Clinical Research Nurse responsibility, thereby increasing the overall number of enrollments and visits. The Clinical Research Nurse ...
The study load and complexity will increase from the Associate Clinical Research Nurse responsibility, thereby increasing the overall number of enrollments and visits. The Clinical Research Nurse ...
Clinical Study Associate information
See Minnesota salary details
$12.48 - $16.27
3% of jobs
$16.27 - $20.05
18% of jobs
$20.80 is the 25th percentile. Wages below this are outliers.
$20.05 - $23.84
20% of jobs
The median wage is $26.14 / hr.
$23.84 - $27.63
15% of jobs
$27.63 - $31.42
11% of jobs
$31.42 - $35.21
4% of jobs
$38.43 is the 75th percentile. Wages above this are outliers.
$35.21 - $39
5% of jobs
$39 - $42.78
8% of jobs
$42.78 - $46.57
6% of jobs
$46.57 - $50.36
6% of jobs
$50.36 - $54.15
3% of jobs
$12
$30
$54
How much do clinical study associate jobs pay per hour?
What is a clinical study associate?
What is the difference between Clinical Study Associate vs Clinical Research Coordinator?
| Aspect | Clinical Study Associate | Clinical Research Coordinator |
|---|---|---|
| Credentials | Bachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficial | Bachelor's degree in health sciences or related field; certifications like CCRP advantageous |
| Work Environment | Pharmaceutical companies, CROs, clinical trial sites | Hospitals, clinics, research centers |
| Job Focus | Monitoring clinical trials, ensuring protocol compliance, data accuracy | Managing daily trial activities, patient recruitment, data collection |
| Employer & Industry Usage | Commonly employed in pharma and CROs | Primarily in healthcare and academic research settings |
Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.
What are the key skills and qualifications needed to thrive as a clinical study associate, and why are they important?
What are some common challenges clinical study associates face when managing multiple clinical trials simultaneously?

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 will operate across multiple Epic engagements and will be responsible for supporting high-quality delivery across clinical implementations, optimization initiatives, stabilization efforts, and transformation programs.
The Senior Associate will leverage strong Epic clinical application expertise, 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 have demonstrated experience 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, and practice growth initiatives.
This role offers flexibility to be based near any major RSM office
As a Healthcare Consulting Senior Associate, you will need to:
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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.
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Support clinical workflow design, build validation, testing, go-live readiness, post-go-live support, and command center operations during critical milestones.
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Analyze current-state clinical workflows and identify opportunities to improve provider efficiency, nursing workflows, patient safety, documentation quality, throughput, and user adoption.
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Ensure solutions align with Epic Systems best practices, regulatory expectations, and long-term sustainability.
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Support optimization of provider documentation tools, order sets, preference lists, in-basket workflows, clinical decision support, and patient care coordination tools.
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Develop and manage project plans, timelines, dependencies, RAID logs, meeting cadences, status reporting, and overall project execution discipline.
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Coordinate cross-functional teams including physicians, nursing, ancillary departments, IT, training, testing, informatics, and third-party vendors while driving accountability across stakeholders.
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Facilitate working sessions, steering committees, governance meetings, executive updates, and activation readiness planning.
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Help maintain delivery quality, scope control, timeline adherence, and proactive issue escalation throughout engagements.
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Support optimization assessments across Epic clinical workflows, governance models, provider adoption, and operational performance.
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Identify opportunities to improve documentation quality, care coordination, patient access to care, throughput, patient satisfaction, and clinical productivity.
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Translate client pain points into actionable Epic enhancement strategies, future-state workflow designs, and prioritized improvement roadmaps.
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Support proposal development, RFP responses, scopes of work, client presentations, staffing plans, and effort estimates.
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Help create and maintain delivery templates, tools, standards, methodologies, and reusable practice assets.
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Mentor associates and junior team members while participating in interviewing, onboarding, and coaching Epic consultants.
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Contribute to practice growth through strong delivery outcomes, trusted client relationships, and identification of expansion opportunities.
Professional Qualifications:
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Bachelor’s degree in a related field or equivalent professional experience.
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Active Epic certification in at least one clinical Epic application is required.
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4+ years of hands-on Epic clinical implementation, optimization, support, or healthcare operations experience.
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Demonstrated experience supporting Epic clinical projects, implementations, or major workstreams.
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Strong understanding of ambulatory, inpatient, emergency, perioperative, or ancillary clinical workflows.
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Experience managing project plans, risks, timelines, and stakeholder expectations.
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Proven ability to support multiple concurrent engagements.
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Strong written and verbal communication skills.
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Strong interpersonal skills and ability to work directly with physicians, nurses, operational leaders, and client stakeholders.
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Ability to balance billable delivery responsibilities with internal leadership contributions.
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Willingness and ability to travel as needed for client engagements (25%-75%).
Preferred Qualifications:
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Multiple certifications such as Epic Systems Ambulatory, Inpatient Clinical Documentation, Orders, ASAP, Stork, Willow, Cupid, OpTime, Anesthesia, or Healthy Planet, Radiant
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Former Epic Systems experience.
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Clinical background as RN, NP, PA, therapist, pharmacist, or other licensed caregiver.
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Experience serving as a project manager, PMO lead, or Epic workstream lead.
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Experience supporting go-lives and post-go-live stabilization.
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Experience mentoring junior consulting staff.
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Experience contributing to proposals, RFPs, or practice development efforts.
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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 - $161,700
Individuals selected for this role will be eligible for a discretionary bonus based on firm and individual performance.