Clinical Research Associate 2 (m/w/d), IQVIA MedTech

Overview

Are you passionate about advancing healthcare through cutting‑edge medical technology? Join IQVIA MedTech as a Clinical Research Associate 2 / CRA 2 (m/w/d) in home-office throughout Germany and help shape the future of patient care. In this role, you’ll work with innovative medical devices that push the boundaries of what’s possible in diagnostics, monitoring, and treatment. If you’re driven by scientific excellence, thrive in a fast‑evolving environment, and are excited to work at the intersection of clinical research and technology, this is the perfect opportunity to make a lasting impact.

Responsibilities

• Performing site selection, initiation, monitoring and close-out visits on medical devices trials.
• Supporting the development of a subject recruitment plan.
• Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH), ISO14155 guidelines.
• Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution.
• Collaborating with experts at study sites and with client representatives.
• Mentoring less experienced team members, acting as subject matter expert for specific topics or additional tasks might be included.

Qualifications

• University Degree in life science or other scientific discipline or apprenticeship in the health care field.
• Minimum of two years of on-site monitoring experience, alternatively an equivalent combination of education, training and experience.
• Working experience in medical devices trial is preferred, but not mandatory.
• Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• In depth knowledge of applicable medical devices guideline ISO14155.
• Strong written and verbal communication skills, attention to detail and ability to work in a fast-paced environment.
• Fluency in German on at least C1 level and a good command of English. Additional language skills in any other European language would be a plus.
• Flexibility to conduct business travel up to about 40-50% of working time. This contains mainly business travel within Germany and can additionally involve business travel to Austria and/or Switzerland.
• Strong IT skills including proficiency in Microsoft Office (Word, Excel, PowerPoint).
• Preferrable driver’s license class B.

What You Can Expect

• Permanent contract.
• Home-Office and flexible work schedules.
• Company car, accident insurance and more.
• Resources that promote your career growth.

We invite you to join IQVIA.

Whatever your career goals, we are here to ensure you get there!

Please apply with your English CV and motivation letter as well as your education certificates and job reference letters (Arbeitszeugnisse).

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.