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Clinical Research Associate II – Contract Based
PSI CRO AG. Work on the frontline of communication with project stakeholders .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical research project management, including on-site monitoring, compliance, and stakeholder communication. Proficient in managing timelines and ensuring data quality while maintaining strong relationships with clinical sites and investigators.
Highest-signal resume keywords
On-Site Monitoring ExperienceClinical Research Project ManagementCRF Review and Source Document VerificationFull Working Proficiency in English and PortugueseMS Office Proficiency
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
On-Site MonitoringClinical Research ComplianceData Quality AssuranceFeasibility ResearchQuery ResolutionStudy Startup ParticipationTimelines ManagementClinical Site ManagementMonitoring Visit TypesRegulatory Document Preparation
Soft Skills
Communication SkillsCollaboration SkillsProblem-Solving SkillsAbility to MultitaskTeamwork
Industry Keywords
Clinical TrialsPhase IIPhase IIIStakeholder CommunicationQuality ControlClinical SitesInvestigatorsData CompliancePortugalLife Sciences
About the role
Key responsibilities & impact- Work on the frontline of communication with project stakeholders
- Ensure timelines, targets and standards of clinical research projects
- Build and maintain relationships with clinical sites and investigators
- Focus on subjects’ rights, safety and well-being and quality of data compliance
- Conduct and report all types of onsite monitoring visits
- Participate in study startup
- Perform CRF review, source document verification and query resolution
- Manage site communication and management
- Supervise study activities, timelines, and schedules on the country level
- Serve as a point of contact for in-house support services and vendors
- Participate in quality control, including compliance monitoring and report review
- Participate in feasibility research
- Support the regulatory team in preparing documents for study submissions
Requirements
What you’ll need- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- A minimum of 1 year of independent on-site monitoring experience in Portugal
- Experience in all types of monitoring visits in Phase II and/or III
- Full working proficiency in English and Portuguese
- Proficiency in MS Office applications
- Ability to plan, multitask and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
- Ability to travel
Benefits
Comp & perks- Professional development and investment in career success
- Home-based (freelance) work arrangement