Independently manage complex CAPAs from investigation through effectiveness checks and closure. * Lead risk assessments for new services, processes, vendors, systems, and operational changes.
Independently manage complex CAPAs from investigation through effectiveness checks and closure. * Lead risk assessments for new services, processes, vendors, systems, and operational changes.
Clinical Quality Reviewer Ensures compliance with the contract, and program requirements for Clinical Quality Management (CQM) within West Region. To ensure quality care is delivered for ...
Clinical Quality Reviewer Ensures compliance with the contract, and program requirements for Clinical Quality Management (CQM) within West Region. To ensure quality care is delivered for ...
Ensure appropriate escalation, documentation, trending, and management visibility for significant quality issues. Partner cross-functionally to identify recurring themes, systemic risks, and ...
Ensure appropriate escalation, documentation, trending, and management visibility for significant quality issues. Partner cross-functionally to identify recurring themes, systemic risks, and ...
Clinical Quality Management Coordinator
Phoenix, AZ · On-site +1
$71K/yr
Clinical Quality Management Coordinator Job No: 537645 Work Type: Full-time Location: REMOTE OPTIONS, PHOENIX Categories: Administrative Support/Customer Service, Healthcare/Medical Support Level ...
Clinical Quality Management Coordinator
Phoenix, AZ · On-site +1
$71K/yr
Clinical Quality Management Coordinator Job No: 537645 Work Type: Full-time Location: REMOTE OPTIONS, PHOENIX Categories: Administrative Support/Customer Service, Healthcare/Medical Support Level ...
Clinical Quality Specialist
Nashville, TN · On-site
$35.25 - $47/hr
Quality Management Develops and maintains current knowledge of CMS and State quality measure ... Evaluates, validates, and ensures submission Electronic Clinical Quality Measure (eCQM) in ...
Clinical Quality Specialist
Nashville, TN · On-site
$35.25 - $47/hr
Quality Management Develops and maintains current knowledge of CMS and State quality measure ... Evaluates, validates, and ensures submission Electronic Clinical Quality Measure (eCQM) in ...
Director, Clinical Quality Assurance
Plymouth Meeting, PA · On-site +1
Quality Management System * Leads all Clinical Quality Assurance (QA) activities within the company * Develops, implements, and maintains all clinical quality assurance systems, processes, and ...
Director, Clinical Quality Assurance
Plymouth Meeting, PA · On-site +1
Quality Management System * Leads all Clinical Quality Assurance (QA) activities within the company * Develops, implements, and maintains all clinical quality assurance systems, processes, and ...
Clinical Quality Management Analyst
Durham, NC · On-site
$73K - $117K/yr
Based on annual corporate goal achievement and individual performance. $73,698.00 - $117,917.00 Skills Clinical Decision Support (CDS), Clinical Quality Management, Clinical Research, Health Care ...
Clinical Quality Management Analyst
Durham, NC · On-site
$73K - $117K/yr
Based on annual corporate goal achievement and individual performance. $73,698.00 - $117,917.00 Skills Clinical Decision Support (CDS), Clinical Quality Management, Clinical Research, Health Care ...
Clinical Quality Specialist
Indianapolis, IN · On-site +1
$35 - $46.50/hr
Director, Medical Management The Clinical Quality Specialist supports the Clinical Quality Nurse in overseeing the HEDIS quality collection, submission, reporting, and auditing as well as assists ...
Quick apply
Clinical Quality Specialist
Indianapolis, IN · On-site +1
$35 - $46.50/hr
Director, Medical Management The Clinical Quality Specialist supports the Clinical Quality Nurse in overseeing the HEDIS quality collection, submission, reporting, and auditing as well as assists ...
Team Management: Oversee daily operations of a team of 20-25 non-exemptquality assurance clinical technicians, ensuring performance meets department production, quality, and operational standards.
Team Management: Oversee daily operations of a team of 20-25 non-exemptquality assurance clinical technicians, ensuring performance meets department production, quality, and operational standards.
BJC is looking for a Clinical Quality Program Manager! Overview Barnes-Jewish West County Hospital offers highly specialized surgical and medical services in an intimate environment and is known for ...
BJC is looking for a Clinical Quality Program Manager! Overview Barnes-Jewish West County Hospital offers highly specialized surgical and medical services in an intimate environment and is known for ...
Clinical Quality Reviewer
Manhattan, NY · On-site
$80K - $115K/yr
JOB SUMMARY Reports to Team Lead, Clinical Quality and Record Review. Works independently and with ... Develop and manage collaborative relationships with internal/external stakeholders and vendor staff.
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Clinical Quality Reviewer
Manhattan, NY · On-site
$80K - $115K/yr
JOB SUMMARY Reports to Team Lead, Clinical Quality and Record Review. Works independently and with ... Develop and manage collaborative relationships with internal/external stakeholders and vendor staff.
Clinical Quality Nurse
Springfield, IL · On-site
The Clinical Quality Nurse is responsible for performing clinical care reviews using criteria ... Job Relationships Reports to the Quality Incentive Programs Manager Principal Responsibilities ...
Clinical Quality Nurse
Springfield, IL · On-site
The Clinical Quality Nurse is responsible for performing clinical care reviews using criteria ... Job Relationships Reports to the Quality Incentive Programs Manager Principal Responsibilities ...
The Senior Manager, Clinical Quality Assurance supports quality assurance activities related to clinical trials and research conducted during the development of pharmaceuticals, biologics, and ...
The Senior Manager, Clinical Quality Assurance supports quality assurance activities related to clinical trials and research conducted during the development of pharmaceuticals, biologics, and ...
$75K - $128K/yr
Analysis and management of clinical quality data including identifying critical performance issues, trending, and benchmarking of performance at a program level. * Engage physician leadership and ...
$75K - $128K/yr
Analysis and management of clinical quality data including identifying critical performance issues, trending, and benchmarking of performance at a program level. * Engage physician leadership and ...
Director, Clinical Quality Assurance
Cambridge, MA · On-site +1
$168K - $268K/yr
As Director, Clinical Quality Assurance Compliance you will lead quality assurance activities ... Review and manage Quality Agreements with CROs and other vendors, ensuring compliance with agreed ...
Director, Clinical Quality Assurance
Cambridge, MA · On-site +1
$168K - $268K/yr
As Director, Clinical Quality Assurance Compliance you will lead quality assurance activities ... Review and manage Quality Agreements with CROs and other vendors, ensuring compliance with agreed ...
Clinical Quality Analyst
Lincoln, NE · On-site
Responsible for the collection, validation, analysis, and reporting of clinical quality data to ... Ability to manage assigned projects, timeslines, and workflows. 12. Ability to prioritize demands ...
Clinical Quality Analyst
Lincoln, NE · On-site
Responsible for the collection, validation, analysis, and reporting of clinical quality data to ... Ability to manage assigned projects, timeslines, and workflows. 12. Ability to prioritize demands ...
Clinical Quality Specialist
Indianapolis, IN · On-site
$67K/yr
The Clinical Quality Specialist supports the Office of Medicaid Policy and Planning (OMPP) by ... Clinical experience in managed care strongly preferred. Salary Statement : The salary for this ...
Clinical Quality Specialist
Indianapolis, IN · On-site
$67K/yr
The Clinical Quality Specialist supports the Office of Medicaid Policy and Planning (OMPP) by ... Clinical experience in managed care strongly preferred. Salary Statement : The salary for this ...
Quality Manager
$126K - $183K/yr
... The Quality Manager is responsible for coordinating the day-to-day operations of the Quality ... clinical measures, assisting with regulatory agency investigations and survey activities, and data ...
Quality Manager
$126K - $183K/yr
... The Quality Manager is responsible for coordinating the day-to-day operations of the Quality ... clinical measures, assisting with regulatory agency investigations and survey activities, and data ...
Clinical Quality Nurse
Springfield, IL · On-site
$33.21 - $49.83/hr
The Clinical Quality Nurse is responsible for performing clinical care reviews using criteria ... Job Relationships Reports to the Quality Incentive Programs Manager Principal Responsibilities ...
Clinical Quality Nurse
Springfield, IL · On-site
$33.21 - $49.83/hr
The Clinical Quality Nurse is responsible for performing clinical care reviews using criteria ... Job Relationships Reports to the Quality Incentive Programs Manager Principal Responsibilities ...
Senior Manager, Clinical Quality Assurance
North Chicago, IL · On-site
$124K/yr
Primarily responsible for leading the management of GCP quality activities in support of studies and projects across one or more clinical programs to drive proactive quality management, and ensure ...
Senior Manager, Clinical Quality Assurance
North Chicago, IL · On-site
$124K/yr
Primarily responsible for leading the management of GCP quality activities in support of studies and projects across one or more clinical programs to drive proactive quality management, and ensure ...
Clinical Quality Manager information
See salary details
$40K - $47.5K
2% of jobs
$47.5K - $55.1K
6% of jobs
$55.1K - $62.6K
13% of jobs
$64.3K is the 25th percentile. Wages below this are outliers.
$62.6K - $70.2K
17% of jobs
The median wage is $74.8K / yr.
$70.2K - $77.7K
19% of jobs
$77.7K - $85.3K
17% of jobs
$85.6K is the 75th percentile. Wages above this are outliers.
$85.3K - $92.8K
12% of jobs
$92.8K - $100.4K
5% of jobs
$100.4K - $107.9K
3% of jobs
$107.9K - $115.5K
3% of jobs
$115.5K - $123K
2% of jobs
$40K
$79.3K
$123K
How much do clinical quality manager jobs pay per year?
How does a clinical quality manager typically interact with cross-functional teams within a healthcare organization?
What is the difference between Clinical Quality Manager vs Clinical Quality Coordinator?
| Aspect | Clinical Quality Manager | Clinical Quality Coordinator |
|---|---|---|
| Certifications | Quality certifications (e.g., CQE, CQA), healthcare quality credentials | Similar certifications, often entry-level or related to healthcare quality |
| Work Environment | Oversees quality programs, manages teams, develops policies | Supports quality initiatives, assists with data collection and compliance |
| Employer & Industry Usage | Hospitals, clinics, healthcare organizations | Healthcare facilities, outpatient centers, clinics |
| Search & Comparison Intent | Understanding managerial roles in healthcare quality | Entry-level or support roles in healthcare quality |
The Clinical Quality Manager typically holds a leadership role, overseeing quality programs and managing teams, requiring advanced certifications. The Clinical Quality Coordinator supports these initiatives through data collection and compliance tasks, often in entry-level positions. Both roles are vital in healthcare settings, but they differ in responsibilities and seniority.
What are the key skills and qualifications needed to thrive as a clinical quality manager?
What is a clinical quality manager?

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 17 days ago
Job description
Role Objectives:
The Senior Clinical Quality Assurance Associate is responsible for the oversight, implementation, and continuous improvement of GCP quality systems supporting global clinical operations across all clinical activities, including decentralised clinical trials (DCTs) that involve nursing services and in-home patient care. This role provides quality leadership to operational teams by ensuring compliance with ICH GCP, applicable global regulatory requirements, Sponsor expectations, and internal Quality Management System (QMS) processes.
The Ideal Candidate:
- Attention to detail
- Process-driven
- Accountable
- Collaborative
What You'll Do:
- Serve as GCP quality systems SME across global clinical operations.
- Provide QA oversight to Clinical Operations, Nursing, Project Management, Medical Affairs, Pharmacovigilance, Regulatory Affairs, and other operational teams.
- Lead investigations for non-conformances, complaints, protocol deviations, quality events, and compliance issues.
- Independently manage complex CAPAs from investigation through effectiveness checks and closure.
- Lead risk assessments for new services, processes, vendors, systems, and operational changes.
- Review clinical and GCP documentation, including protocols, ICFs, eCRFs, Pharmacy Manuals, Monitoring Plans, and essential documents.
- Oversee decentralized clinical trial activities, including nursing, home healthcare, source documentation, IP handling, and related processes.
- Support QMS records and documentation, including deviations, CAPAs, complaints, change controls, risk assessments, SOPs, forms, templates, and guidance documents.
- Review change controls, support approvals, and lead post-implementation effectiveness reviews.
- Support vendor qualification, audits, requalification, Quality Technical Agreements, and ongoing vendor performance monitoring.
- Support audits and inspections by managing readiness, documentation, responses, corrective action plans, evidence, and commitment tracking.
- Review quality metrics, identify trends and risks, drive improvements, support validation/qualification activities, mentor QA staff, represent Quality on cross-functional projects, escalate significant risks, and promote a culture of quality and compliance.
What You'll Need:
- Bachelor's Degree or higher (preference for pharmaceutical, life sciences, or engineering concentration)
- 3 to 5 years of experience in a quality-related role within a CRO, pharmaceutical, biotechnology, or healthcare organization
- Experience supporting global clinical trials and decentralized clinical trial activities
- Experience supporting Sponsor audits, regulatory inspections, internal audits, and/or supplier audits
- Practical experience with quality investigations, CAPAs, root cause analysis, quality risk assessments, and continuous improvement
- Experience with eQMS, eTMF, Microsoft Office, and quality management software applications
- Working knowledge of GCP regulations and global regulatory expectations, including ICH E6(R3), FDA, EU Clinical Trial Regulation, MHRA, GDPR where applicable, and related requirements
- Strong understanding of Quality Management Systems, risk-based quality management principles, and computerized system validation or validation lifecycle principles
- Practical understanding of GDP, warehousing, logistics, and clinical trial supply processes is advantageous
- Strong analytical, organizational, communication, stakeholder management, mentoring, and influencing skills, with the ability to manage multiple priorities, handle confidential information professionally, and apply a proactive, solutions-focused mindset
Location eligibility applies. Candidates must reside in a U.S. state where the company is authorized to hire. This role is not eligible for residents of: California, Colorado, New York, Washington, New Jersey, Massachusetts, Illinois, Hawaii, and District of Columbia.
What We Offer:
Medical, dental, and vision insurance
FSA, HSA
Voluntary Critical Illness, Hospital Indemnity, and Accident Insurance
Group short-term and long-term disability insurance
Group Life Insurance
401K safe harbor plan and company match
Paid vacation, holiday, sick and volunteer time
Paid maternity & paternity leave
What Sets Us Apart:
WEP Clinical partners with biopharmaceutical Sponsors to help them bring treatments closer to the patients who need them most. Through end-to-end clinical trial delivery, home health services, expanded access programs, and market access consultancy, we provide flexible, fit-for-purpose solutions that support drug development, improve access, and help therapies reach the right patients at the right time. With more than 15 years of global experience, we have supported programs across 150+ countries, combining operational scale with the agility and personalized service of a specialized provider. Our work helps bridge critical gaps in care, ensuring safe, ethical, and efficient access to promising new treatments.
We're Committed to Our Team:
WEP has many initiatives to encourage wellness, growth and development, and team relationships. Check out our LinkedIn Life Page to learn more about our team events and all we do to support our employees.
How We Work at WEP Clinical:
At WEP Clinical, we look for individualswho are conscientious, exercise sound judgment, and engage with others thoughtfully and professionally. We believe excellence is achieved through integrity, accountability, and respect for diverse perspectives - and we are committed to helping our people grow and succeed in an inclusive, supportive environment.
Our Services Include:
Access Programs
Clinical Trial Services
Patient Site Solutions
Clinical Trial Supply
Market Access and Commercialization
Data Privacy Notice:
WEP Clinical is committed to protecting your personal information throughout the recruitment process. By applying, you acknowledge that your personal data will be processed in accordance with our Privacy Policy and Job Applicant Privacy Notice.
Privacy Policy: https://www.wepclinical.com/privacy-policy/
Job Applicant Privacy Notice: https://www.wepclinical.com/Job-Applicant-Privacy-Notice/
How to Apply:
To be considered for this role, please submit your resume through the WEP Clinical Careers Portal or by using LinkedIn's Easy Apply option. Please ensure your resume is in English.
Important Note:
To streamline our hiring process, we use an Upwage AI screener. If you receive a link from Upwage, it is a legitimate part of our application process and helps ensure every candidate is reviewed consistently. If you are selected to move forward after the screener, a member of our team will contact you directly from an @wepclinical.com email address to guide you through the next steps of the interview process. Please ensure you apply only through our official careers page (https://www.wepclinical.com/careers/) or our verified LinkedIn page.
For Your Safety, Please Note:
We will nevercommunicate with you via Microsoft Teams or text message
We will never ask for your bank account information at any stage of recruitment
WEP Clinical is a smoke-free, drug-free, and alcohol-free work environment.
WEP Clinical is an equal-opportunity employer. WEP Clinical does not unlawfully discriminate against employees or applicants for employment based on an individual's race, colour, religion, creed, sex, sexual orientation, gender identity or expression, national origin, genetic information, age, disability, marital status, veteran status or any other status protected by applicable law. This policy applies to all terms, conditions, and privileges of employment, including recruitment, hiring, placement, compensation, promotion, discipline, and termination. WEP Clinical will make reasonable accommodation for qualified individuals with known disabilities, in accordance with applicable law.
#LI-Fulltime #LI-remote
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
About WEP Clinical
Sourced by ZipRecruiter
Company size
11 - 50 Employees
Headquarters location
Morrisville, NC, US
Year founded
2008