Company Description Jobsbridge Dear Associate, We have this following position open. Please respond if interested. Title : Clinical QA Lead Location : Boston, MA Duration : 6+ Months 1. Minimum of 5 ...
Company Description Jobsbridge Dear Associate, We have this following position open. Please respond if interested. Title : Clinical QA Lead Location : Boston, MA Duration : 6+ Months 1. Minimum of 5 ...
Clinical Study Quality Lead, Associate Director
Boston, MA · On-site
$39.75 - $53/hr
The Clinical Study Quality Lead (SQL), Associate Director is responsible for advanced quality assurance oversight of clinical trial operations and applicable vendors, across a range of study phases ...
Clinical Study Quality Lead, Associate Director
Boston, MA · On-site
$39.75 - $53/hr
The Clinical Study Quality Lead (SQL), Associate Director is responsible for advanced quality assurance oversight of clinical trial operations and applicable vendors, across a range of study phases ...
Clinical Study Quality Lead, Associate Director
$39.75 - $53/hr
The Clinical Study Quality Lead (SQL), Associate Director is responsible for advanced quality assurance oversight of clinical trial operations and applicable vendors, across a range of study phases ...
Clinical Study Quality Lead, Associate Director
$39.75 - $53/hr
The Clinical Study Quality Lead (SQL), Associate Director is responsible for advanced quality assurance oversight of clinical trial operations and applicable vendors, across a range of study phases ...
Liaise with Vertex clinical functions and external parties including CROs, Vendors and investigator sites to promote high levels of quality and consistency across and within programs. * Provides QA ...
Liaise with Vertex clinical functions and external parties including CROs, Vendors and investigator sites to promote high levels of quality and consistency across and within programs. * Provides QA ...
The Associate Director provides quality leadership and oversight for manufacturing operations ... Experience with shop floor QA oversight in a commercial or late-stage clinical manufacturing ...
The Associate Director provides quality leadership and oversight for manufacturing operations ... Experience with shop floor QA oversight in a commercial or late-stage clinical manufacturing ...
Liaise with Vertex clinical functions and external parties including CROs, Vendors and investigator sites to promote high levels of quality and consistency across and within programs. * Provides QA ...
Liaise with Vertex clinical functions and external parties including CROs, Vendors and investigator sites to promote high levels of quality and consistency across and within programs. * Provides QA ...
The Associate Director provides quality leadership and oversight for manufacturing operations ... Experience with shop floor QA oversight in a commercial or late-stage clinical manufacturing ...
The Associate Director provides quality leadership and oversight for manufacturing operations ... Experience with shop floor QA oversight in a commercial or late-stage clinical manufacturing ...
The Associate Director, GMP Operational Quality Assurance is a Quality leader and advanced ... Drive Quality readiness for major development milestones including IND/IMPD submissions, clinical ...
The Associate Director, GMP Operational Quality Assurance is a Quality leader and advanced ... Drive Quality readiness for major development milestones including IND/IMPD submissions, clinical ...
The Associate Director, GMP Operational Quality Assurance is a Quality leader and advanced ... Drive Quality readiness for major development milestones including IND/IMPD submissions, clinical ...
The Associate Director, GMP Operational Quality Assurance is a Quality leader and advanced ... Drive Quality readiness for major development milestones including IND/IMPD submissions, clinical ...
Associate Director, Manufacturing Process and Technical Quality Assurance Cell and Genetic Therapies
Boston, MA · On-site
$156K - $234K/yr
General Summary: The Manufacturing Process & Technical Quality Associate Director provides end-to-end l quality oversight for cell and gene therapy programs across clinical development ...
Associate Director, Manufacturing Process and Technical Quality Assurance Cell and Genetic Therapies
Boston, MA · On-site
$156K - $234K/yr
General Summary: The Manufacturing Process & Technical Quality Associate Director provides end-to-end l quality oversight for cell and gene therapy programs across clinical development ...
Associate Director, Manufacturing Process and Technical Quality Assurance Cell and Genetic Therap...
Boston, MA · Hybrid
$156K - $234K/yr
General Summary: The Manufacturing Process & Technical Quality Associate Director provides end-to-end l quality oversight for cell and gene therapy programs across clinical development ...
Associate Director, Manufacturing Process and Technical Quality Assurance Cell and Genetic Therap...
Boston, MA · Hybrid
$156K - $234K/yr
General Summary: The Manufacturing Process & Technical Quality Associate Director provides end-to-end l quality oversight for cell and gene therapy programs across clinical development ...
The Clinical Study Quality Lead (SQL), Associate Director is responsible for advanced quality assurance oversight of clinical trial operations and applicable vendors, across a range of study phases ...
The Clinical Study Quality Lead (SQL), Associate Director is responsible for advanced quality assurance oversight of clinical trial operations and applicable vendors, across a range of study phases ...
The Clinical Study Quality Lead (SQL), Associate Director is responsible for advanced quality assurance oversight of clinical trial operations and applicable vendors, across a range of study phases ...
The Clinical Study Quality Lead (SQL), Associate Director is responsible for advanced quality assurance oversight of clinical trial operations and applicable vendors, across a range of study phases ...
Managing Clinical Director
Boston, MA · On-site
$86K - $118K/yr
... and Associates, partnering with market operations leadership, and driving consistency across ... Deliver a full spectrum of high-quality clinical services-including restorative care such as inlays ...
Managing Clinical Director
Boston, MA · On-site
$86K - $118K/yr
... and Associates, partnering with market operations leadership, and driving consistency across ... Deliver a full spectrum of high-quality clinical services-including restorative care such as inlays ...
Managing Clinical Director
$86K - $118K/yr
... and Associates, partnering with market operations leadership, and driving consistency across ... Deliver a full spectrum of high-quality clinical services-including restorative care such as inlays ...
Managing Clinical Director
$86K - $118K/yr
... and Associates, partnering with market operations leadership, and driving consistency across ... Deliver a full spectrum of high-quality clinical services-including restorative care such as inlays ...
Managing Clinical Director
$86K - $118K/yr
... and Associates, partnering with market operations leadership, and driving consistency across ... Deliver a full spectrum of high-quality clinical services--including restorative care such as ...
Quick apply
Managing Clinical Director
$86K - $118K/yr
... and Associates, partnering with market operations leadership, and driving consistency across ... Deliver a full spectrum of high-quality clinical services--including restorative care such as ...
Regulatory Associate
Boston, MA · On-site +1
We are seeking a detail-oriented Regulatory Associate to join our Regulatory Affairs team. In this ... Collaborate with internal teams, such as clinical, quality, and product development, to ensure ...
Regulatory Associate
Boston, MA · On-site +1
We are seeking a detail-oriented Regulatory Associate to join our Regulatory Affairs team. In this ... Collaborate with internal teams, such as clinical, quality, and product development, to ensure ...
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Clinical Data Associate
Boston, MA · On-site
$50K - $62K/yr
The Data Associate is responsible for the quality control of patient data on one or more studies, working with Clinical Research Associates at member institutions, physicians and statisticians ...
Quick apply
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Clinical Data Associate
Boston, MA · On-site
$50K - $62K/yr
The Data Associate is responsible for the quality control of patient data on one or more studies, working with Clinical Research Associates at member institutions, physicians and statisticians ...
Clinical Trial Associate
Needham, MA · On-site
$88K - $100K/yr
The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... Ensure the quality of data submitted from assigned study tasks and timely data submission ...
Clinical Trial Associate
Needham, MA · On-site
$88K - $100K/yr
The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... Ensure the quality of data submitted from assigned study tasks and timely data submission ...
Clinical Trial Associate
Needham, MA · On-site
$88K - $100K/yr
The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... Ensure the quality of data submitted from assigned study tasks and timely data submission ...
Quick apply
Clinical Trial Associate
Needham, MA · On-site
$88K - $100K/yr
The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... Ensure the quality of data submitted from assigned study tasks and timely data submission ...
Clinical Quality Associate information
See Woonsocket, RI salary details
$12.21 - $15.91
3% of jobs
$15.91 - $19.62
18% of jobs
$20.35 is the 25th percentile. Wages below this are outliers.
$19.62 - $23.33
20% of jobs
The median wage is $25.58 / hr.
$23.33 - $27.03
15% of jobs
$27.03 - $30.74
11% of jobs
$30.74 - $34.45
4% of jobs
$37.60 is the 75th percentile. Wages above this are outliers.
$34.45 - $38.15
5% of jobs
$38.15 - $41.86
8% of jobs
$41.86 - $45.57
6% of jobs
$45.57 - $49.27
6% of jobs
$49.27 - $52.98
3% of jobs
$12
$30
$52
How much do clinical quality associate jobs pay per hour?
As of Aug 16, 2026, the average hourly pay for clinical quality associate in Woonsocket, RI is $30.22, according to ZipRecruiter salary data. Most workers in this role earn between $20.29 and $39.86 per hour, depending on experience, location, and employer.
What is the difference between Clinical Quality Associate vs Clinical Research Coordinator?
| Aspect | Clinical Quality Associate | Clinical Research Coordinator |
|---|---|---|
| Required Credentials | Typically a bachelor's degree in life sciences or related field; certifications like CQA are a plus | Bachelor's degree in health sciences, biology, or related field; often requires research-specific certifications |
| Work Environment | Quality assurance departments, regulatory compliance teams, pharmaceutical or biotech companies | Clinical trial sites, hospitals, research institutions |
| Employer & Industry Usage | Used in pharmaceutical, biotech, and healthcare industries focusing on quality and compliance | Common in academic, hospital, and clinical research settings |
The Clinical Quality Associate primarily focuses on ensuring compliance with quality standards and regulatory requirements within the industry, while the Clinical Research Coordinator manages the day-to-day operations of clinical trials. Both roles require strong attention to detail and knowledge of clinical processes but differ in their core responsibilities and work environments.
What are the main challenges clinical quality associates face when ensuring compliance across multiple clinical trial sites?
Clinical Quality Associates often encounter the challenge of maintaining consistent quality and regulatory compliance across diverse clinical trial sites, each with their own procedures and personnel. Coordinating with site staff, monitoring documentation, and ensuring adherence to Good Clinical Practice (GCP) guidelines require strong communication and organizational skills. Additionally, adapting to frequent regulatory updates and handling discrepancies in real time can be demanding, but these challenges also offer opportunities to develop expertise in quality assurance processes and regulatory requirements.
What are the key skills and qualifications needed to thrive as a clinical quality associate?
To thrive as a Clinical Quality Associate, you need a solid understanding of clinical research processes, regulatory compliance, and quality assurance principles, typically supported by a degree in life sciences or a related field. Familiarity with Good Clinical Practice (GCP) guidelines, clinical trial management systems (CTMS), and quality management software is often required. Strong attention to detail, analytical thinking, and effective communication skills make candidates stand out in this role. These skills ensure clinical trials adhere to regulatory standards and deliver reliable, high-quality data for patient safety and successful study outcomes.
What is a clinical quality associate?
Clinical Quality Associates are professionals who support the quality assurance processes within clinical trials or healthcare settings. They are responsible for ensuring that clinical practices comply with regulatory requirements, internal protocols, and industry standards. Their duties often include auditing clinical documents, monitoring study processes, and identifying areas for improvement. By maintaining high-quality standards, Clinical Quality Associates help ensure patient safety and the integrity of clinical data.
Job description
Company Description
Jobsbridge
Job Description
Dear Associate,
We have this following position open. Please respond if interested.
Title : Clinical QA Lead
Location : Boston, MA
Duration : 6+ Months
1. Minimum of 5-8 years of experience providing Software QA and Testing services.
2. Proven track record to perform all aspects of Quality Assurance, such as planning QA activities, providing input into requirements / specification / design.
3. Should have worked in large projects to create or support the creation of test plans, scenarios, test cases and test data, execute approved test plans and report/document results of executed test plans.
4. Document and manage software defects, using a bug tracking system, and report defects to the respective team members.
5. Experience in Bio pharma / Biotechnology / Clinical Research Organization.
6. Exposure to Automation Testing.
7. Exposure/Experience to Mobile tester.
8. Experience with agile software practices and strong knowledge of Jira.
11. Good knowledge of SQL is must.
12. Must have knowledge of HP Quality Center 10.x or higher version.
Best Regards,
Mike Curtis
Additional Information
All your information will be kept confidential according to EEO guidelines.
About Jobsbridge Institute
Sourced by ZipRecruiter
Josbridge Institute is your one-stop destination for your Data, Cloud and Analytics learning needs, powered by Microsoft AI & Cloud platform. We offer a wide range of courses and programs, from foundational to advanced focusing on Data Analysis, Cloud Engg, AI-ML required for Microsoft certification. Our courses are designed to equip you with the practical skills and knowledge required for success in the field of cloud computing, AI and Data Analytics. With our experienced faculty, applied learning and comprehensive curriculum, we are committed to helping you achieve your career goals. Students seeking Internship (CPT & OPT) may apply.
Industry
Business schools and computer and management training
Company size
11 - 50 Employees
Headquarters location
Campbell, CA, US
Year founded
2022