Clinical Research Associate II (CRA II)| Germany| Hybrid

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.

Preferred Qualifications

• 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)

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.