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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in coordinating complex clinical research studies, managing study protocols, and ensuring compliance with regulatory requirements. Proficient in data analysis, participant recruitment, and developing research project plans.
Highest-signal resume keywords
Clinical Research CoordinationStudy Protocol ManagementData AnalysisParticipant RecruitmentRegulatory Compliance
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Research Project PlanningData InterpretationQualitative Data AnalysisQuantitative Data AnalysisProtocol AmendmentsStudy Design ModificationsAdverse Event ReportingRecord-Keeping SystemsQuestionnaire DevelopmentScientific Literature Review
Soft Skills
CollaborationCommunicationProblem-SolvingOrganizational SkillsInterpersonal Skills
Industry Keywords
Public HealthEpidemiologyBehavioral MedicineClinical ResearchSociologyAnthropologyUrban PlanningIRB ManagementGrant ProposalsStudy Databases
About the role
Key responsibilities & impact- Assist investigators as coordinator of complex clinical research studies
- Coordinate multiple research studies and liaise with the school, sponsoring agency, community, and study participants
- Assist in developing research project plans and interpreting results
- Collaborate on manuscripts and grant proposals
- Assist with protocol amendments and study design modifications
- Develop forms, questionnaires, research techniques, and instructional procedure manuals
- Review scientific literature and previous studies
- Implement, manage, and ensure timely completion of study/protocol phases
- Assist with participant recruitment plans
- Ensure compliance with protocol and regulatory requirements
- Establish record-keeping systems and maintain study databases
- Assess participant progress and record results
- Analyze, investigate, and report adverse events
- Resolve IRB/protocol management issues and recommend corrective action
- Liaise with funding or sponsoring agencies
- Evaluate and interpret moderately complex qualitative and quantitative data
- Prepare presentations, reports, analyses, recommendations, and conclusions
Requirements
What you’ll need- Bachelor’s degree or combination of education and/or experience may substitute for minimum education
- At least 2 years of Public Health work experience
- Preferred: 1 year of Public Health, Epidemiological, Behavioral Medicine, Psychological, Sociological, Anthropological, Clinical, or Urban Planning Research experience
- Ability to assist with clinical research studies and manage study protocols
- Pre-employment screening required for external candidates receiving an offer, including criminal background check and applicable additional checks
- No specific certification/professional license required
- Driver’s license not required
Benefits
Comp & perks- Up to 22 days of vacation
- 10 recognized holidays
- 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
- 4 weeks of caregiver leave to bond with your new child
- Family 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
