Clinical Research Conflict of Interest (COI) Analyst

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profile Job Location:

Fairfax, VA - USA

profile Monthly Salary: Not Disclosed
Posted on: 30+ days ago
Vacancies: 1 Vacancy

Department:

Clinical Research

Job Summary

Description

Inova Office of Research Quality Assurance team is seeking a dedicated Clinical Research Conflict of Interest (COI) Analystto join the team.This role will be full-time Monday Friday Hybrid Day shift.

Inova is consistently ranked as a national healthcare leader in safety quality and patient experience. We are also proud to be consistently recognized as a top employer in both the D.C. metro area and the nation.

Featured Benefits:

  • Committed to Team Member Health: offering medical dental and vision coverage and a robust team member wellness program.

  • Retirement: Inova matches the first 5% of eligible contributions starting on your first day.

  • Tuition and Student Loan Assistance: offering up to $5250 per year in education assistance and up to $10000 for student loans.

  • Mental Health Support: offering all Inova team members their spouses/partners and their children 25 mental health coaching or therapy sessions per person per year at no cost.

  • Work/Life Balance: offering paid time off paid parental leave flexible work schedules and remote and hybrid career opportunities.

Clinical Research Conflict of Interest (COI) Analyst Job Responsibilities:

  • Review and analyze potential conflicts of interest from annual and researchspecific disclosures.

  • Develop document and monitor COI management plans including review of financial disclosures RCOI documentation and IDM reports.

  • Provide guidance to investigators and study teams on COI policies disclosure requirements and compliance expectations.

  • Ensure ethical and highquality participant recruitment screening and retention with attention to diversity and equitable inclusion.

  • Conduct monitoring activities such as informed consent verification source data review regulatory binder assessments and evaluation of PI and CRC responsibilities.

  • Perform internal sponsor and regulatorystyle audits; distinguish routine vs. forcause audits; identify triggers such as deviations or safety concerns; and prepare detailed audit reports with corrective action recommendations.

  • Support internal auditing functions and contribute to training related to COI GCP/GLP and clinical research compliance.

  • Collaborate with crossfunctional teams to strengthen research regulatory infrastructure and operational processes.

  • Engage in ongoing professional development to stay current with evolving regulations and best practices.

Minimum Qualifications:

Education:

Bachelors degree in science/healthcare or research related field.

Experience:

  • Two years of relevant work experience addressing conflicts of interest and applying regulations for an academic medical center or the equivalent experience in a related area of healthcare hospital or research administration preferred.

  • Demonstrated experience working in a confidential time-sensitive professional environment.

  • Strong analytical and investigative skills required to elicit information and clarify information professionally and diplomatically.

  • Ability to maintain confidentiality of sensitive matters and exercise discretion

  • Excellent organizational skills.

  • The ability to meet competing deadlines.

  • Ability to learn new tasks and effectively execute them.

  • Willingness and flexibility to take on new assignments while appropriately re-prioritizing tasks.

  • Aptitude to work independently and exercise personal judgment when appropriate.

  • Excellent written/oral communication and proofreading skills.

  • Computer knowledge and skills necessary to accomplish tasks associated with position.

Preferred Qualifications:

  • Experience working with FDA-regulated IND/IDE clinical trials.

  • In-depth understanding of ICH-GCP guidelines and their practical application.

  • Hands-on experience developing Corrective and Preventive Action (CAPA) plans.

  • Proven involvement in SOP authorship review or revision.

  • Direct participation in conducting both on-site and remote monitoring visits to assess site compliance with protocol GCP and regulatory requirements.

  • Auditing and monitoring experience desired.

  • Qualified candidates must be able to effectively communicate with all levels of the organization.




Required Experience:

IC

DescriptionInova Office of Research Quality Assurance team is seeking a dedicated Clinical Research Conflict of Interest (COI) Analystto join the team.This role will be full-time Monday Friday Hybrid Day shift.Inova is consistently ranked as a national healthcare leader in safety quality and patie...
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