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ERGOMED

Clinical Research Associate II – French Speaking

ERGOMED

. Perform national travel and on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visits .

Posted 10/9/2026full-timeRemote • SpainSeniorWebsite

Core Competencies

Role fit
Core 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 complex areas such as oncology and rare diseases. Proficient in regulatory submissions and capable of training site staff while ensuring compliance and quality throughout the study.

Highest-signal resume keywords
On-Site Monitoring ExperiencePhase 2/3 TrialsRegulatory SubmissionsBilingual Proficiency in English and FrenchTraining Investigational Site Staff

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical ResearchMonitoring VisitsInvestigational Site AssessmentRegulatory ComplianceTrial Planning
Soft Skills
Communication SkillsCollaboration SkillsProblem-Solving SkillsMultitasking AbilityTeamwork
Industry Keywords
Life SciencesOncologyRare DiseaseClinical TrialsInvestigational Sites

About the role

Key responsibilities & impact
  • Perform national travel and on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visits
  • Ensure investigational site facilities and staff remain adequate throughout the study
  • Identify investigators and verify their qualifications, resources, facilities, equipment, and staff
  • Train investigational site staff as necessary
  • Support preparation of regulatory and/or EC submissions when applicable
  • Help bring safe and effective pharmaceutical treatments to patients through clinical research

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 and French
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • Ability to travel

Benefits

Comp & perks
  • Flexible/remote work arrangement
  • Work-life balance
  • Career growth opportunities
  • Collaborative international team environment