Mid Level Associate Director Clinical Quality Assurance Jobs
Mid level associate director clinical quality assurance jobs go to professionals ready to own quality systems end to end, guide junior staff through audit cycles, and make regulatory decisions with limited oversight. Hiring runs across Healthcare & Medical Services, Consulting & Professional Services, and Technology & Software, with 23% remote or hybrid availability, and employers like Innophos, GT Independence, and IES Communications competing for associates at this level now.
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Showing 5 of 368+ Mid Level Associate Director Clinical Quality Assurance jobs
What You Will Do
- Coordinate activities within the Quality Assurance Program for the Clinical Research Unit. (20%)
- Perform extensive quality assurance review of study documents and data across multiple complex studies of different therapeutic areas and phases and report findings to management and research team. (30%)
- Assist the Quality Program Manager in regard to specific departmental activities with the goal of maximizing efficiency of management control systems, programs, policies, work methods and procedures. Establish and implement process improvement projects. (20%)
- Ensures that clinical trials are initiated, documented and reported in compliance with internal SOPs, GCP guidelines, sponsor guidelines and current applicable regulatory regulations. (20%)
- Create and maintain an education and training program for the Clinical Trial Unit. (10%)
Additional Responsibilities
- Performs other duties as assigned.
- Complies with all policies and standards.
- For specific duties and responsibilities, refer to documentation provided by the department during orientation.
- Must abide by all requirements to safely and securely maintain Protected Health Information (PHI) for our patients. Annual training, the UH Code of Conduct and UH policies and procedures are in place to address appropriate use of PHI in the workplace.
Education
- Bachelor's Degree or 10 years of either clinical research experience or quality assurance experience or combination of both (Required)
- Master's Degree (Preferred)
Work Experience
- 5+ years of either quality assurance or quality control experience or clinical research experience or combination of both; (Required)
- 3+ years of clinical research management experience including sound knowledge of US regulatory requirements for clinical research including FDA, ICH/GCP (Required)
Knowledge, Skills, & Abilities
- Outstanding organizational skills, oral and written communication skills and strong attention to detail. (Required proficiency)
- Strong interpersonal skills and ability to work as an effective team leader. (Required proficiency)
- Sound knowledge of state and federal regulatory guidelines. (Required proficiency)
- Detail-oriented person with the ability to work independently on multiple tasks and manage time effectively. (Required proficiency)
- Medical terminology comprehension. (Required proficiency)
- Ability to self-monitor progress and complete assigned tasks independently. (Required proficiency)
- Good judgment, initiative and problem solving skills. (Required proficiency)
- Ability to follow through and consistently demonstrate primary job responsibilities are current. (Required proficiency)
- Excellent computer skills with working knowledge / proficiency in a variety of software environments (ie Excel, Access, Word, database applications) and ability to learn document management systems (Required proficiency)
Licenses and Certifications
- Society of Clinical Research Associates (SoCRA) (Preferred)
- ACRP Certified Professional (ACRP-CP) (Preferred)
Physical Demands
- Standing Occasionally
- Walking Occasionally
- Sitting Constantly
- Lifting Rarely 20 lbs
- Carrying Rarely 20 lbs
- Pushing Rarely 20 lbs
- Pulling Rarely 20 lbs
- Climbing Rarely 20 lbs
- Balancing Rarely
- Stooping Rarely
- Kneeling Rarely
- Crouching Rarely
- Crawling Rarely
- Reaching Rarely
- Handling Occasionally
- Grasping Occasionally
- Feeling Rarely
- Talking Constantly
- Hearing Constantly
- Repetitive Motions Frequently
- Eye/Hand/Foot Coordination Frequently
Travel Requirements
- 10%
What You Will Do
- Coordinate activities within the Quality Assurance Program for the Clinical Research Unit. (20%)
- Perform extensive quality assurance review of study documents and data across multiple complex studies of different therapeutic areas and phases and report findings to management and research team. (30%)
- Assist the Quality Program Manager in regard to specific departmental activities with the goal of maximizing efficiency of management control systems, programs, policies, work methods and procedures. Establish and implement process improvement projects. (20%)
- Ensures that clinical trials are initiated, documented and reported in compliance with internal SOPs, GCP guidelines, sponsor guidelines and current applicable regulatory regulations. (20%)
- Create and maintain an education and training program for the Clinical Trial Unit. (10%)
Additional Responsibilities
- Performs other duties as assigned.
- Complies with all policies and standards.
- For specific duties and responsibilities, refer to documentation provided by the department during orientation.
- Must abide by all requirements to safely and securely maintain Protected Health Information (PHI) for our patients. Annual training, the UH Code of Conduct and UH policies and procedures are in place to address appropriate use of PHI in the workplace.
Education
- Bachelor's Degree or 10 years of either clinical research experience or quality assurance experience or combination of both (Required)
- Master's Degree (Preferred)
Work Experience
- 5+ years of either quality assurance or quality control experience or clinical research experience or combination of both; (Required)
- 3+ years of clinical research management experience including sound knowledge of US regulatory requirements for clinical research including FDA, ICH/GCP (Required)
Knowledge, Skills, & Abilities
- Outstanding organizational skills, oral and written communication skills and strong attention to detail. (Required proficiency)
- Strong interpersonal skills and ability to work as an effective team leader. (Required proficiency)
- Sound knowledge of state and federal regulatory guidelines. (Required proficiency)
- Detail-oriented person with the ability to work independently on multiple tasks and manage time effectively. (Required proficiency)
- Medical terminology comprehension. (Required proficiency)
- Ability to self-monitor progress and complete assigned tasks independently. (Required proficiency)
- Good judgment, initiative and problem solving skills. (Required proficiency)
- Ability to follow through and consistently demonstrate primary job responsibilities are current. (Required proficiency)
- Excellent computer skills with working knowledge / proficiency in a variety of software environments (ie Excel, Access, Word, database applications) and ability to learn document management systems (Required proficiency)
Licenses and Certifications
- Society of Clinical Research Associates (SoCRA) (Preferred)
- ACRP Certified Professional (ACRP-CP) (Preferred)
Physical Demands
- Standing Occasionally
- Walking Occasionally
- Sitting Constantly
- Lifting Rarely 20 lbs
- Carrying Rarely 20 lbs
- Pushing Rarely 20 lbs
- Pulling Rarely 20 lbs
- Climbing Rarely 20 lbs
- Balancing Rarely
- Stooping Rarely
- Kneeling Rarely
- Crouching Rarely
- Crawling Rarely
- Reaching Rarely
- Handling Occasionally
- Grasping Occasionally
- Feeling Rarely
- Talking Constantly
- Hearing Constantly
- Repetitive Motions Frequently
- Eye/Hand/Foot Coordination Frequently
Travel Requirements
- 10%
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Find JobsMid Level Associate Director Clinical Quality Assurance Job Market
Who's Hiring
Top Industries Hiring
- Healthcare & Medical Services34
- Consulting & Professional Services32
- Technology & Software30
- Biotechnology & Pharmaceuticals25
- Manufacturing23
Mid Level Associate Director Clinical Quality Assurance Jobs: Frequently Asked Questions
How do I get a mid level associate director clinical quality assurance job?
Position yourself by demonstrating ownership of clinical quality processes rather than task execution. Highlight experience leading internal audits, drafting SOPs, managing CAPAs, or supporting regulatory submissions independently. Tailor your resume to show decisions you drove, not just responsibilities you held. Recruiters at this level want evidence of cross-functional collaboration and the ability to resolve quality issues without constant escalation.
Which companies hire mid level associate director clinical quality assurances?
Companies hiring mid level associate director clinical quality assurances right now include Innophos, GT Independence, and IES Communications, based on current listings on Migrate Mate as of July 2026. Hiring at this level covers pharmaceutical manufacturers, contract research organizations, medical device companies, and biotech firms actively scaling their quality and regulatory infrastructure.
Are there remote mid level associate director clinical quality assurance jobs?
Yes, though availability varies by company size and audit requirements. About 23% of mid level associate director clinical quality assurance openings are remote or hybrid as of July 2026, with fully remote roles more common in companies with distributed clinical operations or centralized quality oversight functions that don't require on-site lab or manufacturing presence.
How do I move up to a mid level associate director clinical quality assurance role?
Progression into mid level typically comes from building ownership across the full quality lifecycle, not just executing discrete tasks. Focus on leading audits from planning through closeout, mentoring newer team members, and contributing to regulatory submissions or inspection readiness. Demonstrating measurable impact, such as reduced audit findings or faster CAPA closure rates, signals readiness to operate at the associate director level.
Which industries hire the most mid level associate director clinical quality assurances?
Mid Level associate director clinical quality assurance roles concentrate in Healthcare & Medical Services, Consulting & Professional Services, and Technology & Software, based on current listings on Migrate Mate as of July 2026. These sectors drive hiring because they face ongoing regulatory scrutiny, require robust quality management systems, and need experienced professionals who can operate independently within complex compliance frameworks.