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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical research management, including oversight of IRB, RDRC, and FDA submissions, while providing leadership to research teams. Proficient in developing policies, managing trial protocols, and ensuring compliance with grant and regulatory standards.
Highest-signal resume keywords
Clinical Research ManagementIRB, RDRC, and FDA SubmissionsSupervisory ExperienceBasic Life Support CertificationPhlebotomy Experience/Certification
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Research ExperiencePolicy DevelopmentTrial ManagementFinancial MonitoringProtocol Assessment
Soft Skills
Critical ThinkingTeam LeadershipEffective CommunicationProblem-Solving
Tools & Technologies
University Systems
Certifications & Qualifications
Basic Life Support CertificationSOCRA CertificationACRP Certification
Industry Keywords
Clinical TrialsGrant ComplianceFDA RegulationsMulti-Center TrialsPatient Care Setting
About the role
Key responsibilities & impact- Provides leadership and oversight to Radiology clinical research programs
- Oversees IRB, RDRC, and FDA submissions
- Provides comprehensive information and support to clinical research staff
- May perform duties delegated to a Clinical Research Coordinator III and/or Clinical Research Supervisor
- Assists with day-to-day management of the research team
- Utilizes critical thinking in clinical trial management
- Develops and implements policies and procedures
- Directs clinical research personnel
- Supervises the research team, including hiring, terminating, scheduling, and performance reviews
- Onboards, educates, and trains new staff
- Identifies personnel and study-conduct problems and implements corrective action plans
- Provides higher-level oversight across the study/protocol lifecycle
- Assists with clinical research strategic planning, trial bandwidth evaluation, protocol assessment, and staff assignments
- Orders supplies for research projects and the research group
- Assists with monitoring finances, recruitment milestones, and personnel resources
- Assists financial and grant administrators with federal and sponsor-funded trials
- Researches and recommends methods and procedures to maintain standards and improve quality
Requirements
What you’ll need- Bachelor’s degree or combination of education and/or experience may substitute for minimum education
- Basic Life Support certification from the American Heart Association or American Red Cross
- 4 years of clinical or research experience
- 1 year of supervisory experience
- Ability to work in a normal office environment, patient care setting, and around blood-borne pathogens
- Ability to travel to various on- and off-campus locations
- Preferred: phlebotomy experience/certification
- Preferred: SOCRA/ACRP certification
- Preferred: familiarity with University systems
- Preferred: effective working knowledge of investigator-initiated, industry-sponsored, and NIH-funded multi-center trials of all phases
- Preferred: knowledge of grant compliance and FDA regulations
Benefits
Comp & perks- Up to 22 days of vacation, 10 recognized holidays, and sick time
- Competitive health insurance packages with priority appointments and lower copays/coinsurance
- Free Metro transit U-Pass for eligible employees
- Defined contribution (403(b)) Retirement Savings Plan, with employee and university contributions starting at 7%
- Wellness challenges, annual health screenings, mental health resources, mindfulness programs and courses, employee assistance program (EAP), financial resources, access to dietitians, and more
- 4 weeks of caregiver leave to bond with your new child
- Family care resources for continued childcare needs
- Adult care resources
- Tuition coverage for employees and family, including dependent undergraduate-level college tuition up to 100% at WashU and 40% elsewhere after seven years