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

TN Germany; Frankfurt; Remote; EUR 50.000 - 70.000; Vollzeit

Zusammenfassung

Join a leading global contract research organization as a Clinical Research Associate in Frankfurt. This role offers career growth, professional development, and the opportunity to work in a supportive environment. You will perform site visits, ensure compliance with regulatory standards, and collaborate with experts in the field. With flexible schedules and home-office options, this position is ideal for those looking to advance their careers in clinical research.

Leistungen

Home-office options

Company car

Insurance

Career growth resources

Flexible schedules

Qualifikationen

• At least one year of on-site monitoring experience.
• Knowledge of GCP and ICH guidelines.

Aufgaben

• Performing site selection, initiation, monitoring, and close-out visits.
• Ensuring site practices meet regulatory standards (GCP, ICH).
• Collaborating with study site experts and client representatives.

Kenntnisse

Communication

Attention to Detail

Fluency in German

English Proficiency

Ausbildung

University Degree in life sciences

Jobbeschreibung

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Clinical Research Associate (m/w/d), Single Sponsor, Frankfurt

Client: IQVIA

Location: Frankfurt, Germany

Job Category: Other

EU work permit required: Yes

Job Reference: 8292afa2b842

Job Views: 1

Posted: 16.05.2025

Expiry Date: 30.06.2025

Job Description:

Join IQVIA as a sponsor-dedicated Clinical Research Associate / CRA (m/w/d) home-based throughout Germany. Enjoy the stability and resources of a leading global contract research organization while gaining direct experience with our client. Whether starting out or seeking to deepen your expertise, this role offers career growth and professional development with access to top-tier training and mentoring. Gain experience across various therapeutic areas in a supportive environment.

Responsibilities include:

• Performing site selection, initiation, monitoring, and close-out visits
• Supporting subject recruitment planning
• Ensuring site practices meet regulatory standards (GCP, ICH)
• Tracking regulatory submissions, recruitment, CRF completion, and data queries
• Collaborating with study site experts and client representatives
• Remote monitoring, study start-up, or therapeutic specialization depending on client model

Qualifications:

• University Degree in life sciences or healthcare-related apprenticeship
• At least one year of on-site monitoring experience
• Knowledge of GCP and ICH guidelines
• Strong communication skills, attention to detail, ability to work in a fast-paced environment
• Fluency in German (C1 level) and good command of English
• Willingness to travel 40-60%
• Driver’s license class B

What we offer:

• Resources supporting your career growth
• Supportive leadership and flexible schedules
• Therapeutic knowledge development programs
• Dynamic work environments and new experiences
• Home-office options, company car, insurance, and more

We are committed to your career goals. Join IQVIA today!

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

#CRASDAJD

IQVIA is a global leader in analytics, technology, and clinical research services for the life sciences industry. We aim to push the boundaries of human and data science to make a positive impact on global health. Learn more at