Clinical Research Associate (all levels) - Germany

Evestia Clinical Group; Deutschland; Hybrid; EUR 45.000 - 65.000; Vollzeit

Benefits dieser Stelle

Annual leave 28 days

Company pension €125/mo

Travel allowance

Corporate card

Health budget

Bonus

Home office allowance

Flexible and hybrid work

Training program

Zusammenfassung

Evestia Clinical is seeking a Clinical Research Associate (CRA of all levels) to protect participant rights and ensure accurate, verifiable data in line with source documentation.

Responsibilities include regulatory-compliant visits, trial development, and liaison between sponsors and sites. Omnichannel communication and strict adherence to GCP are essential for success.

Qualifikationen

• Undergraduate degree or equivalent experience.
• Oncology experience is a must.
• Fluency in English and German required.
• Understanding of GCP and trial regulations.
• Strong written and verbal communication skills.
• Ability to travel nationally and internationally.

Aufgaben

• Perform all visit types and ensure regulatory and protocol compliance.
• Participate in all aspects of a clinical trial from development to study closure.
• Assess safety and efficacy of investigational products per SOPs.
• Maintain KPIs and timelines per company standards.
• Ensure sites comply with protocol objectives and study plans.
• Collaborate in project teams and report to Clinical Team Lead/Project Manager.
• Liaise between sponsors, investigators, and project teams.
• Complete administrative tasks (expense and time reporting) per guidelines.
• Perform other duties as assigned.

Kenntnisse

Oncology experience

English fluency

German fluency

Communication skills

Medical terminology

IT skills

Teamwork

Travel ability

Ausbildung

Undergraduate degree

Jobbeschreibung

We are building something EPIC.

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

Ourfoundation 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.

About the Role

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.

What will your job look like?

• 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.

What will you need to succeed?

• 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

What we offer you in return?

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 experience working here.

Here is a quick look at the benefits you can expect as a valued member of the Evestia Clinical team

• 28 days annual leave
• Company pension scheme of €125 per month,
  Incl. a 15% co-payment on individual employee insurance contracts relating to occupational pension schemes
• Monthly travel allowance for the job ticket
• Non-cash benefit per month (corporate card, insurance CPP)
• Company health budget for individuals
• Variable annual bonus
• Annual home office allowance
• Flexible and hybrid work
• Training and Personal Development Program

Our Commitment to Inclusion and Diversity

We are deeply proud of our people and the successes we achieve together. We actively seek out and hire individuals with diverse backgrounds, voices, beliefs, and perspectives to join our growing global workforce.

At Evestia Clinical, we believe that each person is unique. We celebrate your individuality, knowing that diverse viewpoints fuel Innovation and drive Excellence. We foster true Partnership across our global teams, guided by genuine Care for our colleagues. Our managers are dedicated to upholding this inclusive environment in every aspect of employment - hiring and promotion to training and benefits.

It's who we are, it's what we do, it's what we care about.

Equal Opportunity & Accessibility

Evestia Clinical is an equal opportunity employer committed to diversity in the workplace. We ensure fair treatment of all applicants and employees, without discrimination based on actual or perceived race, color, creed, religion, national origin, age, sex, gender identity or expression, sexual orientation, disability, veteran status, or any other characteristic protected by applicable law.

We are committed to providing accessibility accommodations to applicants with physical and/or mental disabilities. If you are interested in applying for employment with Evestia Clinical and require an accommodation or special assistance during the application process, please notify our recruitment team by sending an email with your request to [e-mail]