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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in on-site monitoring for phase 2/3 clinical trials, particularly in oncology and rare diseases, while ensuring compliance with regulatory standards. Proficient in training site staff and managing dynamic team environments across multiple languages.
Highest-signal resume keywords
On-Site Monitoring ExperiencePhase 2/3 TrialsRegulatory SubmissionsFull Working Proficiency in English, Spanish & PortugueseTraining Investigational Site Staff
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 Trial MonitoringRegulatory ComplianceInvestigational Site AssessmentStudy Conduct ManagementData Collection and Analysis
Soft Skills
Communication SkillsCollaboration SkillsProblem-Solving SkillsMultitasking AbilityTeamwork
Industry Keywords
Life SciencesOncology TrialsRare Disease TrialsInvestigational SitesClinical Research
About the role
Key responsibilities & impact- Perform on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities in Spain and Portugal
- Ensure facilities and investigational site staff remain adequate for study conduct
- Identify investigators and verify their qualifications, resources, facilities, equipment, and staff throughout the study period
- Train investigational site staff as necessary
- Support preparation of regulatory and/or EC submissions when applicable
Requirements
What you’ll need- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- Extensive on-site monitoring experience in phase 2/3 trials
- Ideally, experience with complex trials such as oncology / rare disease
- Full working proficiency in English, Spanish & Portuguese
- Ability to plan, multitask and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
- Ability to travel
Benefits
Comp & perks- Collaborative, international team environment
- Career growth opportunities
- Flexible working
- Work-life balance
- Opportunity to make an impact in meaningful clinical research
- Supportive culture
- Team of experts in clinical research, pharmacovigilance, and quality consulting