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Clinical Research Coordinator Experience
Lifelancer. Attend Medpace’s Virtual CRA Info Session on Wednesday, November 4th from 6-7pm ET on Microsoft Teams if selected .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in conducting clinical research activities, including site qualification, monitoring, and compliance with regulatory requirements. Proficient in managing documentation, communication with site staff, and ensuring adherence to good clinical practices.
Highest-signal resume keywords
Clinical Research CoordinationRegulatory ComplianceRisk-Based MonitoringMicrosoft Office ProficiencyStrong Communication Skills
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Site QualificationMonitoring VisitsProtocol Deviation CommunicationAdverse Event ReviewData VerificationMedical Record ReviewPatient Recruitment AssessmentMonitoring Report CompletionCorrective Action IdentificationInvestigational Product Accountability
Soft Skills
Detail-OrientedTime ManagementPresentation Skills
Tools & Technologies
Microsoft Teams
Certifications & Qualifications
Qualified Clinical Research CoordinatorResearch Nurse
Industry Keywords
Good Clinical PracticeSOPsClinical ResearchHealth SciencesInvestigational Products
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Attend Medpace’s Virtual CRA Info Session on Wednesday, November 4th from 6-7pm ET on Microsoft Teams if selected
- Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol
- Communicate with medical site staff, including coordinators, clinical research physicians, and site staff
- Verify investigator qualifications, training, resources, facilities, laboratories, equipment, and staff
- Verify medical records and research source documentation against case report form data
- Inform site staff of entry errors and ensure good documentation practices
- Communicate protocol deviations according to SOPs, GCP, and applicable regulatory requirements
- Conduct on-site and virtual/remote monitoring using a risk-based monitoring approach and centralized data review
- Identify site deviations/deficiencies and corrective/preventive actions
- Verify that investigators enroll only eligible subjects
- Review regulatory documents
- Maintain medical device and/or investigational product/drug accountability and inventory
- Verify and review adverse events, serious adverse events, concomitant medications, and corresponding illnesses
- Assess patient recruitment and retention success and suggest improvements
- Complete monitoring reports and follow-up letters summarizing findings, deviations, deficiencies, and recommended actions
- Participate in CRA training through the PACE® Training Program and ongoing therapeutic training
Requirements
What you’ll need- Must have a minimum of a Bachelor’s degree in a health or science related field
- Experience as a Clinical Research Coordinator (minimum 2 years)
- Ability to travel 60-70% to locations nationwide is required; some visits may be conducted remotely
- Must maintain a valid driver’s license and the ability to drive to monitoring sites
- Proficient knowledge of Microsoft® Office
- Strong communication and presentation skills
- Must be detail-oriented and efficient in time management
- Qualified Clinical Research Coordinators and Research Nurses
Benefits
Comp & perks- Competitive travel bonus
- Equity/Stock Option program
- Training completion and retention bonus
- Annual merit increases
- 401K matching
- The opportunity to work from home
- Flexible work hours across days within a week
- Retain airline reward miles and hotel reward points
- Home office furniture allowance
- Laptop
- Mobile phone with hotspot for internet access anywhere
- In-house travel agents
- Reimbursement for airline club
- Opportunity for leadership positions – Lead CRA, CRA Manager, Clinical Trial Manager, Training and Development Manager, and many more
- CRA training program (PACE®)
- Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts
- In-house administrative support for all levels of CRAs
- Opportunities to work with international team of CRAs
- Comprehensive health, wellness, retirement, and PTO benefits
- Office based culture with occasional WFH that provides flexibility for eligible positions after training
- Company-sponsored social events
- Industry renowned onboarding and training programs
- Ongoing training and continuous learning opportunities throughout your career