JOB DETAILS
Clinical Research Associate II (CRA II)| Germany| Hybrid
CompanyEvidenze
LocationEssen
Work ModeOn Site
PostedOctober 14, 2026
About The Company
Evidenze is more than a full service CRO, is a full value CRO with Global reach.
Unlike traditional 'full-service' CROs, we go beyond execution.
Our 'Full Value' approach combines deep expertise, cutting-edge technology, and strategic insights to accelerate your trials, optimize costs, and ensure regulatory success.
About the Role
Join us
As a Clinical Research Associate (CRA II), you will play a key role in ensuring the successful delivery of clinical trials while maintaining the highest standards of GCP, ICH-GCP compliance, and regulatory requirements. You will work closely with investigative sites, study teams and external partners to ensure studies are conducted efficiently, ethically and in accordance with protocol requirements.
Key Responsibilities
- Conduct and manage site selection, site initiation, monitoring and close-out visits.
- Ensure clinical trials are conducted in compliance with study protocols, Good Clinical Practice (GCP) guidelines, applicable regulations and standard operating procedures.
- Monitor study progress, including regulatory approvals, patient recruitment, CRF completion and query management.
- Review CRFs in line with the monitoring plan and study requirements.
- Support communication and coordination between investigative sites and external vendors, including central laboratories.
- Ensure appropriate reporting and follow-up of adverse events.
- Identify, document and support the management of protocol deviations and corrective action plans.
- Contribute to the preparation, review and maintenance of clinical trial documentation and study files.
- Support site payment management activities.
- Collaborate effectively with multidisciplinary teams to ensure successful study delivery.
Essential Requirements
- Degree in a Life Sciences or Health Sciences discipline, such as Pharmacy, Biochemistry, Biology or a related field.
- Master's Degree in Clinical Research or equivalent professional experience.
- Previous experience working as a Clinical Research Associate (CRA) within Clinical Trials.
- Strong knowledge of GCP, ICH-GCP, and current clinical trial regulations.
- Fluent German and English communication skills, both written and spoken.
- Willingness and availability to travel as required.
- Strong organisational, planning and communication skills.
- Ability to work independently while contributing effectively within a team environment.
- Previous experience in Onco-Haematology / Oncology Clinical Trials.
- Additional language skills beyond English.
What we offer
- Permanent full-time employment contract.
- Hybrid working model combining remote work and office-based collaboration.
- Opportunity to join a well-established and growing organisation within the clinical research sector.
- Continuous professional training and development.
- Supportive leadership and a collaborative team environment.
- Clear opportunities for professional growth and career progression.
- Competitive salary aligned with experience, skills and qualifications.
- Immediate start available.
Location & Working Model
Germany
Hybrid Working (combination of remote and office-based work)
Hybrid Working (combination of remote and office-based work)
Ready for Your Next Career Move?
If you are an experienced CRA, passionate about Clinical Monitoring, Clinical Trials, and delivering high-quality research in compliance with GCP/ICH-GCP standards, we would love to hear from you.
Apply today and become part of a team committed to driving meaningful progress in healthcare and clinical research.
Apply today and become part of a team committed to driving meaningful progress in healthcare and clinical research.
About us
We are Evidenze, an international healthcare company that operates as a “Full Value” CRO, specializing in clinical research and the generation of scientific evidence. We support pharmaceutical and biotechnology companies throughout the entire product lifecycle, from early-stage research to real-world studies.We combine scientific expertise, technology, and strategic consulting to transform data into actionable insights, improve clinical practice, and deliver real value to the healthcare system.
Key Skills
Clinical researchGCP complianceICH-GCPSite monitoringRegulatory complianceProtocol managementCRF reviewAdverse event reportingSite selectionClinical trial documentationOncology clinical trialsCommunication skillsOrganizational skillsData managementGerman languageEnglish language
Categories
HealthcareScience & ResearchConsulting
Benefits
Permanent full-time employment contractHybrid working modelProfessional training and developmentSupportive leadershipCollaborative team environmentCareer progression opportunities
Job Information
📋Core Responsibilities
You will manage clinical trial site activities including selection, initiation, monitoring, and close-out visits while ensuring compliance with GCP and study protocols. Additionally, you will coordinate with investigative sites and multidisciplinary teams to oversee patient recruitment, data management, and adverse event reporting.
📋Job Type
permanent employee
📊Experience Level
5-10
💼Company Size
12
📊Visa Sponsorship
No
💼Language
English
🏢Working Hours
40 hours
Apply Now →
You'll be redirected to
the company's application page