Clinical Research Coordinator
Duke Careers
Posted: 10/21/2026
Clinical Research Coordinator A/B – Rehabilitation Medicine
University of Pennsylvania Perelman School of Medicine
Posted: 10/21/2026
Senior Manager, Clinical Data Management
Gilead Sciences
Posted: 10/21/2026Google Cloud PlatformOracle
Senior Manager, Clinical Data Management
Gilead Sciences
Posted: 10/21/2026Google Cloud PlatformOracle
Senior Clinical Research Specialist
Duke Careers
Posted: 10/21/2026
Distinguished Scientist, Clinical Research, Thoracic Malignancies
MSD
Posted: 10/21/2026
Clinical Research Associate II
BeOne Medicines
Posted: 10/21/2026
Associate Director, AI Clinical Scientist
Otsuka Pharmaceutical Companies (U.S.)
Posted: 10/21/2026PyTorchTensorflow
Director – Clinical Research Physician, Pain
Eli Lilly and Company
Posted: 10/21/2026
Senior Clinical Study Manager
Intuitive
Posted: 10/21/2026
Overnight Clinical Research Nurse – PRN
ICON plc
Posted: 10/21/2026
Clinical Trial Manager
Iovance Biotherapeutics, Inc.
Posted: 10/20/2026Clinical Research Project Manager – Hybrid
University of Pennsylvania Perelman School of Medicine
Posted: 10/20/2026
Clinical Trial Manager, Senior – Oncology
Boehringer Ingelheim
Posted: 10/20/2026Google Cloud Platform
Clinical Research Project Manager – A-B
Penn Information Systems & Computing
Posted: 10/20/2026Clinical Research Associate
ICON plc
Posted: 10/20/2026
Clinical Research Associate
Syneos Health
Posted: 10/20/2026Senior Clinical Research Associate
ICON plc
Posted: 10/20/2026
Clinical Research Associate – Sponsor Dedicated
IQVIA
Posted: 10/20/2026
Senior Clinical Research Associate – Psychiatry
Worldwide Clinical Trials
Posted: 10/20/2026Clinical Research Coordinator
Duke CareersPosted 10/21/2026full-timeDurham • North Carolina • United StatesJuniorMid-Level💰 $61,026 - $101,959 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical research operations, including data collection, regulatory compliance, and participant management. Proficient in maintaining study documentation and ensuring adherence to institutional policies.
Highest-signal resume keywords
Clinical Research ExperienceData Collection and AnalysisRegulatory ComplianceREDCap ProficiencyParticipant Recruitment and Screening
About the role
Key responsibilities & impact- Participate in or lead day-to-day operations of clinical research studies in the Sweitzer Lab
- Collect, compile, document, and analyze clinical research data
- Perform regulatory and administrative tasks and maintain proper study documentation
- Recruit and screen participants
- Schedule and communicate with participants
- Obtain informed consent
- Manage inventory and accountability of investigational products
- Assist with fMRI sessions
- Administer surveys and questionnaires
- Document adverse events
- Maintain enrollment logs
- Maintain and order equipment
- Develop and submit documentation for Institutional Review Board review in iRIS
- Maintain recruitment and retention rates and evaluate processes
- Conduct study visits in compliance with protocols
- Enter and collect data and develop data-entry or collection SOPs/tools
- Ensure compliance with institutional requirements and policies
- Communicate with IRB staff and reviewers and handle issues appropriately
- May oversee junior staff and train or mentor others
Requirements
What you’ll need- Completion of an associate’s degree
- Minimum of two years of relevant research experience
- A Bachelor’s degree may substitute for 2 years required experience
- Minimum one year of clinical research experience preferred
- Experience or interest in working with addiction populations preferred
- Experience working in REDCap preferred
- Familiar with Duke systems and processes preferred
- Excellent attention to detail
- Strong interpersonal skills
- Willingness to learn
- Flexible schedule, including occasional evening and weekend study visits
- Some evening and weekend flexibility to accommodate participant scheduling needs
Benefits
Comp & perks- Health insurance plans
- Medical and dental care programs
- Generous paid time off
- Retirement programs with employer contributions
- Tuition assistance for employees and their children
- Family-friendly and cultural programs
- Occasional remote work opportunities
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Data EntryDocumentation ManagementSurvey AdministrationAdverse Event DocumentationInventory ManagementFMRI Session AssistanceSOP DevelopmentIRB SubmissionEnrollment Log MaintenanceStudy Visit Compliance
Soft Skills
Attention to DetailInterpersonal SkillsWillingness to LearnFlexibility
Tools & Technologies
REDCapIRISDuke Systems
Industry Keywords
Clinical ResearchAddiction PopulationsInstitutional Review BoardStudy ProtocolsParticipant Scheduling