Associate Director Clinical Quality Assurance Jobs in Massachusetts
Associate Director Clinical Quality Assurance jobs in Massachusetts are concentrated in the Greater Boston area, the Route 128 corridor, and Cambridge, where companies like Biogen, Takeda, and Sanofi Genzyme maintain major operations. Demand is strongest in GCP compliance, clinical trial oversight, and regulatory submissions quality, reflecting the state's dense concentration of biopharma and medical device firms. Massachusetts is among the most active markets in the country for this role, with openings at every seniority level within the director track. Find a role that fits below and apply directly.
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Showing 5 of 6+ Associate Director Clinical Quality Assurance jobs
- Evaluate clinical information received, write and/or review various reports including, but not limited to, Medical Record Reviews, Medical Record Chronologies, Provider Bill Reviews, Coding Reviews, Hospital Bill Reviews, List of Missing Records, Medical Bill Apportionments, Mock Billing Invoice and Medical Summary Statements.
- Perform quality assurance review of peer review reports, correspondences, addendums or supplemental reviews.
- Ensure clear, concise, evidence-based rationales have been provided in support of all recommendations and/or determinations.
- Ensure that all client instructions and specifications have been followed and that all questions have been addressed.
- Ensure each review is supported by clinical citations and references when applicable and verify that all references cited are current and obtained from reputable medical journals and/or publications.
- Ensure the content, format, and professional appearance of the reports are of the highest quality and in compliance with company standards.
- Ensure the appropriate board specialty has reviewed the case in compliance with client specifications and/or state mandates and is documented accurately on the case report.
- Verify that the reviewer has attested to only the facts and that no evidence of reviewer conflict of interest exists.
- Ensure the provider credentials and signature are adhered to the final report.
- Identify any inconsistencies within the report and contacts the Reviewer to obtain clarification, modification or correction as needed.
- Contact the appropriate person to recover any missing documentation or verify charges.
- Assist in resolution of customer complaints and quality assurance issues as needed.
- Ensure all federal ERISA or state mandates are adhered to at all times.
- Provide insight and direction to management on consultant quality, availability and compliance with all company policies and procedures and client specifications.
- Promote effective and efficient utilization of company resources.
- Participate in various continuing education requirements and or training activities.
- Perform other duties as assigned.
- Bachelor/Associate degree in nursing or related field; or minimum five years related experience; or equivalent combination of education and experience.
- Experience with medical terminology, medications, medical specialties and treatment protocols required.
- Experience in the insurance industry preferred.
- Must hold and maintain an unencumbered Registered Nursing license
- Must have strong knowledge of medical terminology, anatomy and physiology, treatment protocols, medications and laboratory values
- Must be a qualified typist with a minimum of 40 W.P.M.
- Must be able to operate a general computer, fax, copier, scanner, and telephone.
- Must be knowledgeable of multiple software programs, including but not limited to Microsoft Word, Outlook, Excel, and the Internet.
- Must possess excellent skills in English usage, grammar, punctuation and style.
- Ability to follow instructions and respond to upper managements’ directions accurately.
- Demonstrates accuracy and thoroughness. Looks for ways to improve and promote quality and monitors own work to ensure quality is met.
- Must demonstrate exceptional communication skills by conveying necessary information accurately, listening effectively and asking questions where clarification is needed.
- Must be able to work independently, prioritize work activities and use time efficiently.
- Must be able to maintain confidentiality.
- Must be able to demonstrate and promote a positive team -oriented environment.
- Must be able to stay focused and concentrate with frequent interruptions.
- Must be able to work well under pressure and or stressful conditions.
- Must possess the ability to manage change, delays, or unexpected events appropriately.
- Demonstrates reliability and abides by the company attendance policy.
- Must maintain a professional and clean appearance at all times consistent with company standards.
- Evaluate clinical information received, write and/or review various reports including, but not limited to, Medical Record Reviews, Medical Record Chronologies, Provider Bill Reviews, Coding Reviews, Hospital Bill Reviews, List of Missing Records, Medical Bill Apportionments, Mock Billing Invoice and Medical Summary Statements.
- Perform quality assurance review of peer review reports, correspondences, addendums or supplemental reviews.
- Ensure clear, concise, evidence-based rationales have been provided in support of all recommendations and/or determinations.
- Ensure that all client instructions and specifications have been followed and that all questions have been addressed.
- Ensure each review is supported by clinical citations and references when applicable and verify that all references cited are current and obtained from reputable medical journals and/or publications.
- Ensure the content, format, and professional appearance of the reports are of the highest quality and in compliance with company standards.
- Ensure the appropriate board specialty has reviewed the case in compliance with client specifications and/or state mandates and is documented accurately on the case report.
- Verify that the reviewer has attested to only the facts and that no evidence of reviewer conflict of interest exists.
- Ensure the provider credentials and signature are adhered to the final report.
- Identify any inconsistencies within the report and contacts the Reviewer to obtain clarification, modification or correction as needed.
- Contact the appropriate person to recover any missing documentation or verify charges.
- Assist in resolution of customer complaints and quality assurance issues as needed.
- Ensure all federal ERISA or state mandates are adhered to at all times.
- Provide insight and direction to management on consultant quality, availability and compliance with all company policies and procedures and client specifications.
- Promote effective and efficient utilization of company resources.
- Participate in various continuing education requirements and or training activities.
- Perform other duties as assigned.
- Bachelor/Associate degree in nursing or related field; or minimum five years related experience; or equivalent combination of education and experience.
- Experience with medical terminology, medications, medical specialties and treatment protocols required.
- Experience in the insurance industry preferred.
- Must hold and maintain an unencumbered Registered Nursing license
- Must have strong knowledge of medical terminology, anatomy and physiology, treatment protocols, medications and laboratory values
- Must be a qualified typist with a minimum of 40 W.P.M.
- Must be able to operate a general computer, fax, copier, scanner, and telephone.
- Must be knowledgeable of multiple software programs, including but not limited to Microsoft Word, Outlook, Excel, and the Internet.
- Must possess excellent skills in English usage, grammar, punctuation and style.
- Ability to follow instructions and respond to upper managements’ directions accurately.
- Demonstrates accuracy and thoroughness. Looks for ways to improve and promote quality and monitors own work to ensure quality is met.
- Must demonstrate exceptional communication skills by conveying necessary information accurately, listening effectively and asking questions where clarification is needed.
- Must be able to work independently, prioritize work activities and use time efficiently.
- Must be able to maintain confidentiality.
- Must be able to demonstrate and promote a positive team -oriented environment.
- Must be able to stay focused and concentrate with frequent interruptions.
- Must be able to work well under pressure and or stressful conditions.
- Must possess the ability to manage change, delays, or unexpected events appropriately.
- Demonstrates reliability and abides by the company attendance policy.
- Must maintain a professional and clean appearance at all times consistent with company standards.
See All 6 Associate Director Clinical Quality Assurance Jobs in Massachusetts
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Find JobsAssociate Director Clinical Quality Assurance Jobs by City in Massachusetts
Where Massachusetts roles are concentrated, by current openings.
Associate Director Clinical Quality Assurance Job Market in Massachusetts
A snapshot from current Massachusetts openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Food & Beverage
- Biotechnology & Pharmaceuticals
- Consulting & Professional Services
What Massachusetts Employers Look For
The qualifications that appear most often in associate director clinical quality assurance jobs across Massachusetts.
- Bachelor's or advanced degree in life sciences, pharmacy, or a related clinical field
- Minimum seven to ten years of quality assurance experience in clinical research or biopharma
- Deep working knowledge of FDA regulations, ICH guidelines, and GCP standards
- Demonstrated experience leading QA audits, CAPA programs, and inspection readiness activities
- Prior people management experience leading QA teams or cross-functional quality initiatives
- Familiarity with electronic quality management systems such as Veeva Vault or MasterControl
Associate Director Clinical Quality Assurance Jobs in Massachusetts: Frequently Asked Questions
How do you become a associate director clinical quality assurance in Massachusetts?
The path to this role in Massachusetts typically begins with a bachelor's or advanced degree in a life sciences field, followed by progressive experience in GCP or GMP quality assurance at a biopharma, biotech, or medical device company. There is no state-issued license specific to this role, but many Massachusetts employers expect candidates to hold or actively pursue credentials such as the ASQ Certified Quality Auditor. Building experience through QA specialist or manager roles at Massachusetts-based companies, then taking on audit leadership and CAPA ownership, is the standard career trajectory.
Which companies hire associate director clinical quality assurances in Massachusetts?
Companies currently hiring associate director clinical quality assurances in Massachusetts include MES Solutions, Elucid, and Korro Bio, per current listings on Migrate Mate as of October 2026. Massachusetts's dense biopharma and medical device ecosystem means openings appear consistently across established multinationals and mid-size clinical-stage companies alike.
Which Massachusetts cities have the most associate director clinical quality assurance jobs?
The cities with the most associate director clinical quality assurance openings in Massachusetts are Norwood, Cambridge, and Boston. Boston and Cambridge anchor the market through their concentration of biopharma headquarters and major academic medical centers, while suburban Route 128 corridor cities attract openings from large clinical operations and device manufacturers that have expanded outside the urban core.
Are there remote associate director clinical quality assurance jobs in Massachusetts?
Yes, and more than many clinical roles, since a significant portion of the work involves document review, audit management, and cross-functional oversight that can be performed remotely. About 67% of associate director clinical quality assurance openings tied to Massachusetts are remote or hybrid as of October 2026, reflecting a post-pandemic shift among Massachusetts biopharma employers. Inspection readiness and on-site audit support tend to remain the parts of the role most anchored to a physical location.
How can I get hired as a associate director clinical quality assurance in Massachusetts with little or no experience?
The most realistic entry path is moving into a QA associate or clinical quality specialist role at a Massachusetts biopharma or CRO, then building toward manager-level ownership of audits and CAPA processes. Large Massachusetts employers such as Biogen, Takeda, and Sanofi Genzyme run structured associate programs and regularly hire from adjacent roles like clinical operations coordinator, regulatory affairs associate, or document control specialist. Earning an ASQ quality credential or completing a GCP certification strengthens candidates coming from adjacent functions and signals readiness for the compliance demands of the associate director level.
Where can I find and apply to associate director clinical quality assurance jobs in Massachusetts?
You can find and apply to associate director clinical quality assurance jobs in Massachusetts on Migrate Mate, which lists current Massachusetts openings from employers actively hiring for this role. Search the listings, find roles that fit your background and target area, and apply directly.
See All 6 Associate Director Clinical Quality Assurance Jobs in Massachusetts
Find roles in Massachusetts that match your experience and apply in just a few clicks.
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