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Digital Start-Up Specialist
Humaneva GroupDigital Start-Up Specialist coordinating clinical trials for Pratia Germany. Managing protocols, medical documentation, study data, and digital systems in a hybrid German role.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in coordinating clinical trials, ensuring compliance with regulatory and quality standards, and effectively managing study-related documentation and data. Proficient in collaborating with diverse stakeholders and utilizing digital applications to enhance study processes.
Highest-signal resume keywords
Clinical Trial CoordinationStudy Protocol ReviewMS Office ProficiencyBilingual Communication (German and English)Organizational Skills
ATS Keywords
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Hard Skills
Clinical Studies ExperienceStudy Documentation ManagementData AnalysisRegulatory ComplianceStudy Procedures Review
Soft Skills
Strong Communication SkillsCollaborationIndependent Working StyleAttention to DetailStructured Organization
Tools & Technologies
MS Office (Word, Excel, PowerPoint)Study-Specific IT SystemsDigital Applications
Industry Keywords
Clinical ResearchStudy CoordinatorInclusion/Exclusion CriteriaStudy-Related DocumentationOn-Site Visits
About the role
Key responsibilities & impact- Coordination and support of clinical trials while ensuring regulatory and quality requirements are met
- Collaboration with study nurses, principal investigators, pharmacists and study coordinators
- Review and analysis of study protocols, study procedures, examination plans, and inclusion/exclusion criteria
- Creation, maintenance and review of medical forms and study-related documentation
- Documentation, analysis and management of study-related data using MS Office applications
- Work with study-specific IT systems and onboarding to new digital applications and processes
- Communication with international team members and external stakeholders in English
- Structured organization and coordination of relevant processes to ensure smooth study conduct
Requirements
What you’ll need- At least two years of experience in clinical studies, ideally as a study coordinator
- Solid understanding of the roles and responsibilities within clinical research teams
- Experience in reviewing and analyzing study protocols
- Experience with medical forms and study-related documentation
- Confident user of MS Office, particularly Word, Excel and PowerPoint
- Strong IT affinity and ability to quickly learn new systems and digital applications
- Willingness to attend on-site visits to study sites, up to monthly and at least quarterly
- Excellent written and spoken German and English
- Structured, careful and independent working style
- Strong organizational skills
- Strong communication skills and enjoyment of collaborating with internal and external contacts
Benefits
Comp & perks- Flexible working hours by arrangement
- 30 days of vacation
- Company-sponsored training
- Support for personal and professional development
- Flat hierarchies and open, transparent communication
- Collaboration within an international professional network
- Diverse development opportunities in Germany and across Europe