Full-Time

Quality Assurance Specialist

Yale University

Yale University

Research university in New Haven, CT

Compensation Overview

$68k - $120.5k/yr

New Haven, CT, USA

Hybrid

Hybrid work model; occasional travel to research sites may be required.

Bachelor's, Master's

Category
Biology & Biotech (1)
Required Skills
Quality Assurance (QA)

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Requirements
  • Demonstrated knowledge and ability to apply International Council for Harmonisation Good Clinical Practice guidelines.
  • Demonstrated knowledge and ability to interpret federal regulations governing human subject research.
  • Ability to be detail oriented while maintaining a broader perspective within a solution-oriented approach to issues.
  • Ability to work, plan, research, and conduct projects with minimal supervision on a flexible schedule.
  • Professionalism, maturity, good judgment, and ability to work with confidential material and protected health information.
  • Ability to handle multiple and diverse projects simultaneously.
  • Strong critical thinking and problem-solving abilities.
  • Advanced interpersonal, oral, and written communication skills and ability to work effectively with a wide variety of external and internal stakeholders.
  • Demonstrated understanding of clinical research processes and procedures from study start-up through study closeout.
  • Bachelor's degree in a related field and five years of related experience, or an equivalent combination of education and experience.
  • Completion of Good Clinical Practice training within three months of hire.
Responsibilities
  • Collaborate with Yale Center for Clinical Investigation leadership, departmental leaders, investigators, Human Research Protection Program, and the Institutional Review Board to facilitate review of human subject research activities for safety, compliance, and clinical-trial integrity.
  • Evaluate clinical trial conduct for compliance with institutional policies, state and federal regulations, and Good Clinical Practice guidelines.
  • Identify research noncompliance and report it to appropriate Yale Center for Clinical Investigation, departmental, Human Research Protection Program, Institutional Review Board, and Office of General Counsel leadership.
  • Provide educational and corrective-action advice to faculty preparing for Food and Drug Administration audits.
  • Serve as liaison among investigators, research teams, and the Food and Drug Administration during inspections; record proceedings and summarize inspection activity in real time.
  • Consult with investigators on data safety monitoring plan details for grant applications.
  • Develop data and safety monitoring plans based on risk-assignment categories.
  • Direct investigators on strengthening research and ensuring regulatory and protocol compliance.
  • Analyze protocols and customize audit plans for protocol-specific benchmarks in addition to standard audit reviews.
  • Assess audit findings in the context of the broader program to identify trends and program-wide areas requiring improvement or education.
  • Assess risk and stratify studies from a quality-assurance and regulatory-compliance perspective based on clinical research experience and regulatory knowledge.
  • Review study participants' medical records and determine the impact of noncompliance with federal regulations, Good Clinical Practice, and university policies on study plans and processes.
  • Exercise judgment in assessing the risk level associated with findings and whether reporting to other regulatory entities is required.
  • Report quality-assurance findings related to deviations and noncompliance in accordance with strict reporting regulations.
  • Review audit reports and findings with investigators and advise on and monitor appropriate action plans.
  • Conduct follow-up reviews for compliance with audit recommendations and respond to investigator rationale.
  • Identify trends in findings requiring educational or corrective actions for specific researcher groups.
  • Design and conduct training programs, recommend quality improvements, and assist with creating and following up on corrective-action plans based on audit findings.
  • Develop and deliver education and training programs promoting safety and compliance for principal investigators and study-team members.
  • Conduct continuous audits, identify high-risk areas, and create activity reports for ongoing medical analysis.
  • Interview individuals with specialized knowledge related to an investigation.
  • Identify areas of concern or heightened medical risk to subjects, investigators, or the university.
  • Integrate data safety and monitoring plans and quality-assurance findings with committees and educational plans.
Desired Qualifications
  • Prior auditing or monitoring experience.
  • Master's degree in a related field.
  • Demonstrated knowledge of quality-assurance auditing and monitoring techniques and practices.
  • Society of Clinical Research Associates or Association of Clinical Research Professionals certification, or equivalent.

Yale University is a private research university in New Haven, Connecticut. It provides undergraduate, graduate, and professional education alongside research, scholarship, and public engagement.

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