Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Fortrea

Clinical Research Associate – DACH

Fortrea

. Identify and assess new potential investigators and sites .

Posted 10/1/2026full-timeRemote • GermanyJuniorMid-LevelWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical research processes, ICH/GCP Guidelines, and regulatory compliance, with a strong ability to monitor site performance and ensure data quality. Proven skills in relationship building and organizational management within a CRO or Pharma environment.

Highest-signal resume keywords
Clinical Research ProcessesICH/GCP GuidelinesMonitoring ExperienceRegulatory ComplianceOrganizational Skills

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

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

Hard Skills
Site MonitoringData Quality AssessmentProtocol ComplianceFeasibility AssessmentRisk Assessment
Soft Skills
Organizational SkillsTime ManagementRelationship Building
Industry Keywords
Clinical TrialsCROPharmaRegulatory AuditsEC Submissions

About the role

Key responsibilities & impact
  • Identify and assess new potential investigators and sites
  • Recommend sites during feasibility and selection phases
  • Conduct pre-study, initiation, monitoring, and close-out visits
  • Monitor site performance, data quality, and protocol compliance
  • Act as a key point of contact for site personnel, providing training and support
  • Use data insights to assess risks and drive decisions
  • Support regulatory audits, EC submissions, and system access coordination

Requirements

What you’ll need
  • University or college degree in life sciences, nursing, pharmacy, or a related allied health profession; equivalent relevant experience may be considered in lieu of formal education
  • Basic to good knowledge of ICH/GCP Guidelines and applicable local laws and regulations governing clinical trials
  • Solid understanding of clinical research processes, regulations, and methodology
  • Strong organizational and time management skills
  • Ability to build and maintain relationships
  • 1 to 3 years of monitoring experience required within CRO or Pharma environment

Benefits

Comp & perks
  • Regional monitoring—minimizing travel while maximizing your impact
  • Supportive environment
  • Opportunity to contribute to meaningful research that improves lives
  • Sponsor-dedicated team with a strong pipeline and purpose