Clinical Trials Office Quality Assurance Analyst

Yale University; New Haven (CT); Hybrid; USD 68,000 - 121,000; Full time

Job summary

Yale University is seeking a Clinical Trials Office Quality Assurance Analyst in New Haven to support quality management for cancer center clinical trials, focusing on QC, monitoring, and inspection readiness. You will coordinate internal monitoring, track deviations and CAPAs, and support timely follow-up to strengthen data integrity.

The role requires collaboration with investigators, HRPP and IRB, and requires expertise in regulatory knowledge and GCP.

Qualifications

• Professionalism, maturity, good judgment and ability to handle confidential material and PHI.
• Self-directed with ability to plan, research and conduct projects with minimal supervision.
• Organized and capable of handling multiple/diverse projects simultaneously.
• Advanced interpersonal, oral and written communications with diverse stakeholders.
• Solid understanding of clinical research processes from start-up to close-out.

Responsibilities

• Facilitate review of activities related to human subject research for safety, compliance and integrity.
• Analyze protocols to customize audit plans for protocol-specific benchmarks.
• Assess risk and stratify studies from QC/regulatory perspective.
• Evaluate trial conduct for compliance with policies, regulations and GCP.
• Review medical records and communicate findings to investigators; assess level of risk.

Skills

Professionalism

Self-directed work

Multitasking

Interpersonal skills

Clinical research processes

Education

Bachelor's Degree in related field

Job description

Clinical Trials Office Quality Assurance Analyst

Department: Comprehensive Cancer Center - Clinical Trial Operations

Working at Yale means contributing to a better tomorrow. Whether you are a current resident of our New Haven-based community, eligible for opportunities through the New Haven Hiring Initiative, or a newcomer, interested in exploring all that Yale has to offer, your talents and contributions are welcome. Discover your opportunities at Yale!

Overview

Reporting to the Manager of Quality and Education, the incumbent supports quality management activities for clinical trials conducted within the YCC Clinical Trials Office (CTO), with a primary focus on quality control, routine monitoring support, and audit/inspection readiness. The incumbent will coordinate internal monitoring activities and documentation, track and trend quality findings (including data delinquency indicators), and support timely follow-up and closure of deviations and CAPAs, including effectiveness checks, to strengthen compliance and data integrity.

The mission of the Quality and Education team is to foster a supportive environment conducive to achieving the Cancer Center’s clinical research mission by promoting consistent, proactive, and inspection-ready clinical research practices that protect participants and support high-quality data.

Essential Duties of the Position

• Works directly and in collaboration with Departmental leaders, investigators, research staff, HRPP and the IRB to facilitate the review the activities associated with human subject research in terms of safety, compliance, and integrity of clinical trials conducted at YCC CTO.
• Analyzes protocols to customize audit plans for protocol specific benchmarks in addition to standard audit reviews.
• Assesses the risk and stratify the study from a QC/regulatory compliance perspective based on clinical research experience and regulatory knowledge.
• Evaluates clinical trial conduct to ensure research integrity and compliance with institutional policies, state and federal regulations, and ICH Good Clinical Practice.
• Reviews medical records of study participants, determines the impact of non-compliance (e.g. violations of federal regulations, GCP and University policies) on study plans/processes, makes judgments and communicates findings to investigators. Exercises judgment in the assessment of the level of risk associated with findings in terms of the need for reporting out to other regulatory entities.
• Reports review findings related to deviations; non-compliance based on very strict reporting regulations.
• Identifies research non-compliance and reports to appropriate leadership within YCC CTO.
• Identifies and develops recommendations for changes that ensure the fulfillment of compliance requirements. Provides direction to investigators to strengthen their research and ensure regulatory and protocol compliance.
• Maintain oversight during an FDA inspection or other internal or external audit. Provides educational and corrective action advice to faculty in preparation for FDA audits.
• Reviews reports/findings from audits with investigators and advises and monitors appropriate action plan.
• Conducts follow-up reviews for compliance with audit recommendations, responding to investigator rationale. Identifies trends in findings to be addressed in educational or corrective actions for specific group of researchers.
• Conducts continuous auditing activities identifying areas of high risk and creates activity reports for ongoing analysis from a medical standpoint. Interviews individuals with specialized knowledge related to an investigation. Identifies areas of concern or heightened medical risk to subjects, investigators, or the University.
• Develops education and training programs to promote safety and compliance for the PI's and all study team members.
• Consults to investigators needing data safety monitoring plan details/information for their grant application. Develops Data and Safety Monitoring Plans based on the risk assignment categories.

Required Skills and Abilities

1. Professionalism, maturity, good judgment, and ability to work with confidential material and protected health information.

2. Self-directed with the ability to work, plan, research, and conduct projects with minimal supervision and on a flexible schedule.

3. Organized and capable of handling multiple/diverse projects simultaneously.

4. Advanced interpersonal, oral and written communications skills and ability to work effectively with a wide variety of external and internal stakeholders.

5. Demonstrable understanding of clinical research processes and procedures from study start-up to study close out.

Preferred Skills and Abilities

1. SOCRA/ACRP (or equivalent) certification

2. Master's Degree in related field

Principal Responsibilities

1. Works directly and in collaboration with YCC CTO leadership, Departmental leaders, investigators, research staff, HRPP and the IRB to facilitate the review the activities associated with human subject research in terms of safety, compliance, and integrity of clinical trials conducted at YCC CTO.
2. Analyzes protocols to customize audit plans for protocol specific benchmarks in addition to standard audit reviews.
3. Assesses the risk and stratify the study from a QC/regulatory compliance perspective based on clinical research experience and regulatory knowledge.
4. Evaluates clinical trial conduct to ensure research integrity and compliance with institutional policies, state and federal regulations, and ICH Good Clinical Practice.
5. Reviews medical records of study participants, determines the impact of non-compliance (e.g. violations of federal regulations, GCP and University policies) on study plans/processes, makes judgments and communicates findings to investigators. Exercises judgment in the assessment of the level of risk associated with findings in terms of the need for reporting out to other regulatory entities.
6. Reports review findings related to deviations; non-compliance based on very strict reporting regulations.
7. Identifies research non‑compliance and reports to appropriate leadership within YCC CTO.
8. Identifies and develops recommendations for changes that ensure the fulfillment of compliance requirements. Provides direction to investigators to strengthen their research and ensure regulatory and protocol compliance.
9. Maintain oversight during an FDA inspection or other internal or external audit. Provides educational and corrective action advice to faculty in preparation for FDA audits.
10. Reviews reports/findings from audits with investigators and advises and monitors appropriate action plan.
11. Conducts follow-up reviews for compliance with audit recommendations, responding to investigator rationale. Identifies trends in findings to be addressed in educational or corrective actions for specific group of researchers.
12. Conducts continuous auditing activities identifying areas of high risk and creates activity reports for ongoing analysis from a medical standpoint. Interviews individuals with specialized knowledge related to an investigation. Identifies areas of concern or heightened medical risk to subjects, investigators, or the University.
13. Develops education and training programs to promote safety and compliance for the PI's and all study team members.
14. Consults to investigators needing data safety monitoring plan details/information for their grant application. Develops Data and Safety Monitoring Plans based on the risk assignment categories.

Required Education and Experience

1. Bachelor’s Degree in related field and five years of related experience or an equivalent combination of education and experience.
2. Comprehensive understanding of clinical research review, approval and Data and Safety Monitoring processes
3. Comprehensive knowledge of federal regulations concerning the protection of human subjects and clinical trial design, implementation and analysis.
4. Advance knowledge of auditing and monitoring techniques and practices.

Job Posting Date

10/23/2026

Job Category

Professional

Bargaining Unit

NON

Compensation Grade

Administration & Operations

Compensation Grade Profile

Manager; Program Leader (24)

Salary Range

$68,000.00 - $120,500.00

Benefits

A general description of the benefits to be offered with this Managerial & Professional position is available at:

Yale Benefits

Time Type

Full time

Duration Type

Staff

Work Model

Hybrid

Background Check Requirements

All candidates for employment will be subject to pre-employment background screening for this position, which may include motor vehicle, DOT certification, drug testing and credit checks basedon the position description and job requirements. All offers are contingent upon the successful completion of the background check. For additional information on the background check requirements and process visit "Learn about background checks" under the Applicant Support Resources section of Careers on the It's Your Yale website.

Health Requirements

Certain positions have associated health requirements based on specific job responsibilities. These may include vaccinations, tests, or examinations, as required by law, regulation, or university policy.

Posting Disclaimer

Salary offers are determined by a candidate’s qualifications, experience, skills, and education in relation to the position requirements, along with the role’s grade profile and current internal and external market conditions.

The intent of this job description is to provide a representative summary of the essential functions that will be required of the position and should not be construed as a declaration of specific duties and responsibilities of the position. Employees will be assigned specific job-related duties throughtheir hiring department.

The University is committed to basing judgments concerning the admission, education, and employment of individuals upon their qualifications and abilities and seeks to attract to its faculty, staff, and student body qualified persons from a broad range of backgrounds and perspectives. In accordance with this policy and as delineated by federal and Connecticut law, Yale does not discriminate in admissions, educational programs, or employment against any individual on account of that individual’s sex, sexual orientation, gender identity or expression, race, color, national or ethnic origin, religion, age, disability, status as a special disabled veteran, veteran of the Vietnam era or other covered veteran.

Inquiries concerning Yale's Policy Against Discrimination and Harassment may be referred to the Office of Institutional Equity and Accessibility (OIEA).

Note

Yale University is a tobacco-free campus.