Clinical Research Associate II (CRA II)| Germany| Hybrid
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Description
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.
- 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.
- 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.
- 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.
Germany
Hybrid Working (combination of remote and office-based work)
Hybrid Working (combination of remote and office-based work)
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.