Clinical Research Associate Germany

We are building something
EPIC.

Evestia Clinical is a biotech-focused global CRO delivering authentic expertise and personalized support where client need it most.

Our foundation is built on four core principles:
Innovation drives us to seek new solutions,
Excellence defines the high standards we keep, and genuine Care ensures a supportive culture for both our patients and our people. We foster Partnership in everything we do, believing that working together—with trust and flexibility—is the key to success.

Our approach is agile by nature and personalized by design. This translates to a workplace where you are empowered to find the creative solutions necessary for our collective success. We offer a welcoming, flexible, and supportive culture that values trust and belonging, ensuring you have the support needed to grow your skills and thrive while making a difference.

We partner with our clients to provide expert knowledge and guidance through complex clinical trials in rare disease, oncology, neurology, immunology, and inflammation. At Evestia Clinical, you will become a vital part of a global specialist CRO. This means you will deliver life changing impact through clinical excellence.

We are committed to creating development opportunities that allow your skills to grow right alongside ours. If you are inspired by this collaborative environment and ready to change the lives of patients worldwide, we’d love to welcome you to our team.

We are looking for a Clinical Research Associate (CRA of all levels) to be responsible for ensuring that the rights and safety of clinical trial participants are protected and that the clinical data obtained are accurate, complete, and verifiable according to source.

• Performing all and any visit types while ensuring regulatory and protocol compliance
• Participate in all aspects of a clinical trial from development and planning to study closure
• Comply with applicable regulations, ICH/GCP and Evestia Clinical or sponsor SOPs to assess the safety and efficacy of investigational products (drugs, biologics or devices)
• Maintain key performance metrics in accordance with company standards and timelines, ensuring compliance with established monitoring and reporting expectations
• Ensure assigned sites are in compliance with the study protocol objectives
• Work in project teams and under supervision, reporting to a Clinical Team Lead and/or Project Manager
• Liaise effectively between sponsors, investigators and project teams
• Completes all administrative tasks (expense and time reporting) within company guidelines
• Perform any other duties as assigned.

• Undergraduate degree or equivalent combination of education, training and experience
• Oncology experience is a must, neurology would be advantageous
• Must be fluent in English & German
• Understanding the principles of Good Clinical Practice (GCP) and clinical trial regulations
• Both written and verbal communication and presentation skills
• Understanding of medical terminology and human physiology
• Proficiency with information technology (computer skills)
• Excellent customer service skills
• Demonstrated flexibility and adaptability
• Ability to work in a team environment and independently as needed
• Ability to travel nationally and internationally as required
• Organizational and time management skills, able to prioritize tasks and work within timelines

We believe that to do your best work, you need the best support. That is why we care deeply about your well-being, personal development, and achieving a true work-life balance. Our comprehensive benefits package is carefully designed to align with our culture and values, ensuring it maximizes your positive…