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Clinical Research Associate
PSI CRO AG. Prepare, conduct, and report selection, initiation, routine, and closeout monitoring visits .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical research processes, including site monitoring, regulatory document management, and effective communication with clinical investigators and project teams. Proficient in delivering training and presentations while maintaining compliance with audit standards.
Highest-signal resume keywords
Clinical Research ExperienceSite MonitoringRegulatory Document ManagementMS Office ProficiencyPatient Care Experience
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
CRF ReviewSource Document VerificationQuery ResolutionFeasibility ResearchStudy-Specific Tracking Systems
Soft Skills
Communication SkillsCollaboration SkillsProblem-Solving SkillsTeamwork AbilityTraining Delivery
Industry Keywords
Life Sciences DegreeClinical EnvironmentInvestigator MeetingsSite IdentificationAudit Compliance
About the role
Key responsibilities & impact- Prepare, conduct, and report selection, initiation, routine, and closeout monitoring visits
- Deliver training to investigators, site staff, and project teams
- Work with complex studies
- Perform CRF review, source document verification, and query resolution
- Manage site communication
- Participate in site identification
- Serve as contact for clinical investigators, vendors, and support services regarding study progress
- Participate in feasibility research
- Prepare and deliver presentations at Investigator’s Meetings
- Prepare for and attend company audits and resolve audit findings
- Support Regulatory Affairs in procuring site regulatory documents
- Maintain study-specific automated tracking systems
Requirements
What you’ll need- Only CVs in English will be considered
- College/University Degree in Life Sciences
- At least 2 years experience in patient care and/or health care or clinical environment
- Full working proficiency in English
- Experience in Clinical Research is a plus
- Availability to travel
- Proficiency in MS Office applications
- Ability to plan and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
Benefits
Comp & perks- Tailored courses and mentoring
- Career development opportunities
- Opportunity to develop as a senior, trainer, mentor, and leader
- Opportunity to advance toward future Lead Monitor roles