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Humaneva Group

Study Nurse, Clinical Trial Coordinator

Humaneva Group

. Provide care and support to study participants throughout the entire course of the study .

Posted 10/14/2026full-timeBerlin • GermanyMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in clinical research support, including participant care, documentation, and regulatory coordination. Proficient in managing study workflows and ensuring high-quality data management while maintaining strong communication in both German and English.

Highest-signal resume keywords
Clinical Research SupportStudy Nurse QualificationAdverse Event ReportingMS Office ProficiencyB2 Level German and English

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
Documentation in CRFsLaboratory ProceduresDiagnostic ExaminationsData ManagementWorkflow Development
Soft Skills
Teamwork SkillsService-Oriented MannerStructured ApproachMeticulousnessInitiative
Tools & Technologies
MS Office
Certifications & Qualifications
Study Nurse Qualification
Industry Keywords
Clinical ResearchRegulatory CoordinationSite Initiation VisitsMonitoring VisitsAudits and Inspections

About the role

Key responsibilities & impact
  • Provide care and support to study participants throughout the entire course of the study
  • Assist with study visits, diagnostic examinations, and laboratory procedures
  • Schedule appointments and document medical data in CRFs and databases
  • Ensure complete, high-quality documentation
  • Assist with adverse event reporting
  • Coordinate with sponsors, CROs, and regulatory authorities
  • Participate in site initiation visits and monitoring visits, including preparation and follow-up
  • Support the preparation, conduct, and follow-up of audits and inspections
  • Contribute to the development of workflows and processes

Requirements

What you’ll need
  • Completed training in a medical or scientific field
  • Additional qualification as a Study Nurse (m/f/d) preferred
  • Initial experience in the clinical research environment is an advantage
  • Good command of German and English (at least B2 level), both written and spoken
  • Proficient in MS Office (Word, Excel, Outlook)
  • Strong teamwork skills, commitment, and initiative
  • Friendly, professional, and service-oriented manner
  • Structured, meticulous, and organized approach to work

Benefits

Comp & perks
  • Flexible working hours by arrangement
  • 30 days of annual leave
  • Employer-sponsored professional development
  • Diverse career development opportunities in Germany and across Europe
  • Team-building activities and team events
  • Opportunities for professional and personal growth
  • Open and transparent communication in a company with flat hierarchies
  • Work in a friendly, experienced, and highly motivated team
  • Exciting professional network with teams in Germany and across Europe