Clinical Research Associate I or II (m/w/d), Single Sponsor

IQVIA Argentina; Frankfurt; Remote; EUR 50.000 - 70.000; Vollzeit

Zusammenfassung

Join a leading global contract research organization as a Clinical Research Associate I or II. This home-based role throughout Germany offers career growth and professional development while managing site visits, ensuring compliance with regulatory standards, and collaborating with experts. Ideal candidates will have a degree in life sciences, monitoring experience, and fluency in German.

Leistungen

Home-office

Company car

Accident insurance

Career growth resources

Flexible work schedules

Qualifikationen

• Minimum of two years of on-site monitoring experience.
• Knowledge of GCP and ICH guidelines.
• Fluency in German (C1 level) and good command of English.

Aufgaben

• Performing site selection, initiation, monitoring and close-out visits.
• Supporting the development of a subject recruitment plan.
• Evaluating the quality and integrity of site practices.

Kenntnisse

Attention to detail

Communication

Flexibility

Ausbildung

University Degree in life science

Apprenticeship in health care

Jobbeschreibung

When you join IQVIA as a sponsor-dedicated Clinical Research Associate I or II (m/w/d) home-based throughout Germany, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our clients. Whether you're just starting out or looking to deepen your expertise, this role promises to offer intentional career growth and professional development. With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.

Your responsibilities will include:

• Performing site selection, initiation, monitoring and close-out visits
• 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) 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
• Depending on client model there might be remote-monitoring, involvement in study start-up processes, specialization on therapeutic area (pharmaceutical product or medical devices)

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
• Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Strong written and verbal communication skills, attention to detail and ability to work in a fast pace environment
• Fluency in German on at least C1 level and a good command of English
• Flexibility to travel up to 40-60% of working time
• Driver’s license class B

What you can expect:

• Resources that promote your career growth
• Leaders that support flexible work schedules
• Programs to help you build your therapeutic knowledge
• Dynamic work environments that expose you to new experiences
• Home-office, company car, accident insurance and more

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

We invite you to join IQVIA.

Please apply with your English CV, motivation letter and your certificates and reference letters.

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 https://jobs.iqvia.com