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

Essen

Full-time

Permanent employee

Join us

At Evidenze, we are passionate about advancing healthcare and improving patients' quality of life. With more than 400 professionals and a comprehensive portfolio of services across clinical research, patient support programmes, medical education, communications and events, we support innovation throughout the healthcare sector.
As part of our continued growth, we are looking for a Clinical Research Associate II (CRA II) to join our Clinical Operations team in Germany. This is an excellent opportunity for an experienced CRA who is looking to take the next step in their career within a collaborative, supportive and well-established organisation.

About the Role

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.

À propos de nous

Antares Consulting est une société internationale de conseil en stratégie, management et technologie, spécialisée dans les domaines de la santé, des sciences de la vie et des services socio-sanitaire.

Nous sommes l'entreprise de référence du secteur ayant travaillé pour plus de 870 clients et avec des bureaux à Barcelone, Madrid, Lisbonne, Paris, Bruxelles et La Paz. Nous fournissons des services et développons des projets pour des clients de plus de 27 différents pays.

Nos clients sont toutes les organisations publiques et privées ayant des intérêts dans le secteur de la santé : hôpitaux, prestataires de soins, administrations publiques, industrie pharmaceutique, biotech et dispositifs médicaux, sociétés de services diverses, investisseurs, etc.

Antares Consulting fait partie de Curis Alliance (https://www.curisalliance.com), un réseau de sociétés de conseil européen spécialisé dans la santé qui comprend Mansfield Advisors (Royaume-Uni) et WMC Healthcare (Allemagne).

Dans le cadre de notre projet d'expansion et de croissance, nous souhaitons intégrer les meilleurs professionnels du marché pour continuer à être la principale société de conseil spécialisée dans le secteur de la santé.