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Study Nurse / Clinical Trial Coordinator (m/f/d)
Humaneva Group. Provide comprehensive care and support to study participants throughout the entire clinical trial process .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in providing comprehensive care and support throughout the clinical trial process, with strong skills in patient education, documentation, and communication with regulatory authorities. Proficient in managing clinical trial logistics and ensuring compliance during inspections and audits.
Highest-signal resume keywords
Clinical Trial SupportPatient EducationDocumentation in CRFsGerman and English ProficiencyMS 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
Clinical Trial SupportDiagnostic ExaminationsDocumentation in CRFsPatient Visit AssistanceAdverse Event Reporting
Soft Skills
Strong Organizational SkillsTeam SpiritFriendly InteractionDetail-Oriented ApproachCommitment and Motivation
Tools & Technologies
Web-Based DatabasesMS Office
Certifications & Qualifications
Study Nurse Qualification
Industry Keywords
Clinical TrialsPatient CareRegulatory AuthoritiesCROsInspections and Audits
About the role
Key responsibilities & impact- Provide comprehensive care and support to study participants throughout the entire clinical trial process
- Deliver empathetic patient education and serve as a knowledgeable point of contact
- Assist with patient visits
- Perform diagnostic examinations and provide support in the laboratory
- Schedule appointments and systematically document medical data in CRFs and web-based databases
- Ensure accurate and complete documentation
- Support the reporting of adverse events
- Communicate with sponsors, CROs, and regulatory authorities
- Participate in site initiation visits and monitoring visits, including their preparation and follow-up
- Prepare for, support, and provide follow-up for inspections and audits
Requirements
What you’ll need- Completed training or education in a medical or life sciences field
- Additional qualification as a Study Nurse preferred
- Experience supporting clinical trials and handling study-related correspondence is an advantage but not essential
- Good written and spoken German and English skills, at least CEFR level B2
- Proficiency in MS Office (Word, Excel, Outlook)
- Strong organizational skills and a structured, detail-oriented approach to work
- Team spirit, commitment, and motivation
- Friendly and professional manner when interacting with study participants, team members, and external partners
Benefits
Comp & perks- Opportunities for professional and personal growth
- Flat hierarchies and open, transparent communication
- Support for personal and professional development
- Opportunity to help shape workflows and processes
- Flexible working hours by arrangement
- Professional network with teams in Germany and across Europe
- Career development opportunities in Germany and across Europe
- 30 days of annual leave
- Employer-supported training and the resources required for the role
- Complimentary beverages
- Monthly team meals
- Team-building activities and team events