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Posted: 10/14/2026Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical research management, including CRA performance evaluation, training, and compliance. Proficient in drug development processes and capable of fostering professional relationships with stakeholders.
Highest-signal resume keywords
Clinical Research ManagementCRA Performance EvaluationDrug Development ProcessSite Monitoring ExperienceFluent in English
About the role
Key responsibilities & impact- Serve as the main point of contact for CRAs for non-project-specific needs
- Manage CRA performance and support training and growth opportunities
- Communicate with CRAs regarding knowledge, understanding, compliance, project goals, and departmental and corporate objectives
- Plan and implement resource solutions for new and ongoing projects with the Resourcing team
- Support corporate strategy and vision for organizational growth
- Participate in CRA recruiting, interviewing, and hiring
- Conduct new employee orientation and onboarding
- Participate in project-related meetings with Clinical Operations leadership
- Ensure ongoing evaluation of CRA performance, including monitoring evaluation visits
- Assist in developing department quality standards and programs
- Assist with Clinical Operations SOP/WI development and review
- Build and maintain professional relationships with internal and external stakeholders
- Review and approve timesheets and discuss CRA utilization
- Conduct monthly calls with direct reports to assess workload, performance, deliverables, priorities, and compliance
- Review and approve non-billable expenses
- Initiate and oversee Performance Improvement Plans for CRAs as required
Requirements
What you’ll need- BA/BS in a Life Science field or commensurate experience
- Demonstrated experience in clinical research
- Prior site monitoring experience, including experience managing CRAs
- In-depth knowledge of the drug development process, including study initiation, clinical monitoring, drug safety, regulatory affairs, data management and analysis, and clinical study report generation
- Ability to travel approximately 20% domestically and internationally
- Fluent in English
Benefits
Comp & perks- Collaborative, international team environment
- Career growth opportunities
- Flexible work arrangements / remote work
- Work-life balance
- Opportunity to contribute to meaningful clinical research that helps bring treatments to patients
- Supportive culture with trust and early ownership
- Passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting
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 MonitoringRegulatory AffairsData ManagementClinical Study Report GenerationPerformance Improvement PlansQuality Standards DevelopmentSOP/WI DevelopmentEmployee OnboardingResource PlanningProject Management
Soft Skills
CommunicationRelationship BuildingTraining and DevelopmentLeadershipProblem Solving
Industry Keywords
Life ScienceClinical OperationsCRA RecruitingCompliancePerformance Monitoring