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Clinical Quality Manager Jobs in Delaware (NOW HIRING)

Clinical QA Specialist

Newark, DE · On-site

$85K - $133K/yr

Clinical QA Specialist Newark, DE, United States Marlborough, MA, United States Are you passionate ... Risk Managers will also be considered. * 5+ years of experience in a similar role, preferably ...

Clinical QA Specialist

Newark, DE · On-site

$85K - $133K/yr

Clinical QA Specialist Newark, DE, United States Marlborough, MA, United States Are you passionate ... Risk Managers will also be considered. * 5+ years of experience in a similar role, preferably ...

Clinical QA Specialist

Newark, DE · On-site

$85K - $133K/yr

At Hologic, we are seeking a Clinical QA Specialist to play a critical role in the investigation ... Risk Managers will also be considered. * 5+ years of experience in a similar role, preferably ...

Clinical QA Specialist

Newark, DE · On-site

$85K - $133K/yr

At Hologic, we are seeking a Clinical QA Specialist to play a critical role in the investigation ... Risk Managers will also be considered. * 5+ years of experience in a similar role, preferably ...

Clinical QA Specialist

Newark, DE · On-site

$85K - $133K/yr

At Hologic, we are seeking a Clinical QA Specialist to play a critical role in the investigation ... Risk Managers will also be considered. * 5+ years of experience in a similar role, preferably ...

Clinical QA Specialist

Newark, DE · On-site

$85K - $133K/yr

At Hologic, we are seeking a Clinical QA Specialist to play a critical role in the investigation ... Risk Managers will also be considered. * 5+ years of experience in a similar role, preferably ...

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Clinical Quality Manager information

See Delaware salary details

$40K

$79.4K

$123.1K

How much do clinical quality manager jobs pay per year?

As of Sep 2, 2026, the average yearly pay for clinical quality manager in Delaware is $79,418.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,100.00 and $88,600.00 per year, depending on experience, location, and employer.

What is a clinical quality manager?

A Clinical Quality Manager is a healthcare professional responsible for ensuring that clinical practices and processes comply with regulatory standards and deliver high-quality patient care. They oversee quality assurance programs, monitor clinical performance, conduct audits, and implement improvement initiatives. Clinical Quality Managers also collaborate with medical staff and administrators to identify areas for improvement and ensure compliance with accreditation requirements. Their goal is to enhance patient outcomes and maintain safety and efficiency in clinical environments.

What are the key skills and qualifications needed to thrive as a clinical quality manager?

To thrive as a Clinical Quality Manager, you need expertise in healthcare regulations, quality improvement methodologies, and a relevant degree such as nursing, public health, or healthcare administration. Familiarity with quality management software, data analysis tools, and certifications like CPHQ (Certified Professional in Healthcare Quality) are commonly required. Outstanding leadership, problem-solving, and communication skills help drive continuous improvement and foster collaboration across departments. These competencies are crucial for ensuring regulatory compliance, enhancing patient safety, and elevating the standard of care in clinical environments.

How does a clinical quality manager typically interact with cross-functional teams within a healthcare organization?

Clinical Quality Managers work closely with a variety of departments, including nursing, medical staff, compliance, and administration, to develop and implement quality improvement initiatives. Their role often involves facilitating meetings, leading training sessions, and ensuring that all teams adhere to clinical guidelines and regulatory standards. Effective collaboration is essential, as the Clinical Quality Manager must gather input from multiple stakeholders to identify areas for improvement and to monitor the impact of quality programs. Building strong relationships and clear communication channels across teams is a key part of success in this position.

What is the difference between Clinical Quality Manager vs Clinical Quality Coordinator?

AspectClinical Quality ManagerClinical Quality Coordinator
CertificationsQuality certifications (e.g., CQE, CQA), healthcare quality credentialsSimilar certifications, often entry-level or related to healthcare quality
Work EnvironmentOversees quality programs, manages teams, develops policiesSupports quality initiatives, assists with data collection and compliance
Employer & Industry UsageHospitals, clinics, healthcare organizationsHealthcare facilities, outpatient centers, clinics
Search & Comparison IntentUnderstanding managerial roles in healthcare qualityEntry-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 most commonly searched types of Clinical Quality jobs in Delaware?

The most popular types of Clinical Quality jobs in Delaware are:

What are popular job titles related to Clinical Quality Manager jobs in Delaware?

For Clinical Quality Manager jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Clinical Quality Manager jobs in Delaware look for?

The top searched job categories for Clinical Quality Manager jobs in Delaware are:

What cities in Delaware are hiring for Clinical Quality Manager jobs?

Cities in Delaware with the most Clinical Quality Manager job openings:

Infographic showing various Clinical Quality Manager job openings in Delaware as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, 4% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $79,418 per year, or $38.2 per hour.

Clinical QA Specialist

Hologic

Newark, DE • On-site

$85K - $133K/yr

Full-time

Re-posted 19 days ago


Hologic rating

8.0

Company rating: 8.0 out of 10

Based on 25 frontline employees who took The Breakroom Quiz

179th of 495 rated machine equipment manufacturers


Job description

Clinical QA Specialist

Newark, DE, United States

Marlborough, MA, United States

Are you passionate about ensuring compliance and patient safety in the medical device industry? At Hologic, we are seeking a Clinical QA Specialist to play a critical role in the investigation and reporting of potential and actual adverse events, as well as other regulatory reporting activities. In this role, you'll collaborate with cross-functional teams, including Technical Service, Marketing, Sales, and Regulatory, to ensure timely and thorough documentation, analysis, and reporting. If you thrive in a fast-paced, collaborative environment and have a strong background in regulatory compliance and quality assurance, this is your opportunity to make a meaningful impact on healthcare innovation.

Knowledge:

  • Comprehensive understanding of FDA Quality System Regulations, ISO 13485, EU Medical Device Regulation, and ISO 14971 for risk management.
  • Strong knowledge of medical procedures and the expected and potential outcomes related to Hologic's product portfolio.
  • Familiarity with post-market surveillance requirements, adverse event reporting, and health risk assessments.
  • Awareness of regulatory reporting processes, including MedWatch reports, notified body communications, and external notifications.

Skills:

  • Proven ability to independently collect, analyze, and assess information associated with adverse events and determine appropriate next steps.
  • Effective communication skills to interact with internal teams, sales personnel, customers, patients, and regulatory agencies.
  • Strong organizational skills to ensure timely documentation, reporting, and follow-up of adverse events and regulatory submissions.
  • Analytical skills to support and lead investigations, including CAPAs, nonconformances, and other quality system processes.
  • Experience in developing metrics and quality reports related to reportable events and identifying potential excursions.
  • Ability to innovate and improve processes to enhance efficiency and compliance with post-market surveillance requirements.
  • Proficient in leading or participating in internal and external audits, inspections, and assessments.

Behaviors:

  • Proactive and detail-oriented, ensuring compliance with regulatory requirements and internal procedures.
  • Collaborative and team-oriented, fostering strong relationships across functions to support investigations and reporting activities.
  • Customer-focused, ensuring communications and responses are timely, accurate, and aligned with patient safety goals.
  • Resilient and adaptable, thriving in a fast-paced and evolving environment.
  • Problem-solving mindset, with a commitment to driving resolution and continuous improvement in quality processes.

Experience:

  • Bachelor's degree in Medicine, Nursing, Biomedical Engineering, Electromedical Engineering, or a related field. Risk Managers will also be considered.
  • 5+ years of experience in a similar role, preferably within the medical device or healthcare industry.
  • Hands-on experience with adverse event reporting, regulatory communications, and health risk assessments.
  • Proven track record in supporting or leading CAPAs, nonconformances, and quality investigations.

Why join Hologic?

We are committed to making Hologic the destination for top talent. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career.

The annualized base salary range for this role is $85,200 - $133,300 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, education, business needs and market demand.

Agency and Third-Party Recruiter Notice

Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition, Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered.

Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.

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