Experienced Clinical Research Associate (m/w/d), Multi-Sponsor

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

Zusammenfassung

Join a leading global provider in clinical research as a Clinical Research Associate in Frankfurt. This role involves managing clinical trials, ensuring compliance with regulations, and collaborating with study teams. Enjoy flexible work options and resources for career growth.

Leistungen

Home-office options

Company car or allowance

Insurance

Pension

Qualifikationen

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

Aufgaben

• Perform site selection, initiation, monitoring, and close-out visits.
• Support development of subject recruitment plan.
• Evaluate quality and integrity of site practices.

Kenntnisse

Communication

Attention to Detail

Flexibility

Ausbildung

University Degree in Life Sciences

Apprenticeship in Healthcare

Jobbeschreibung

Experienced Clinical Research Associate (m/w/d), Multi-Sponsor, Frankfurt

Client: IQVIA

Location: Frankfurt, Germany

Job Category: Other

EU work permit required: Yes

Job Reference: ff1ffb01490c

Job Views: 2

Posted: 16.05.2025

Expiry Date: 30.06.2025

Job Description:

Join IQVIA as a CRA / SrCRA (m/w/d) in our Clinical Site Management department, home-based throughout Germany. You will focus on comprehensive clinical trial management across various indications and learn about diverse scientific approaches from sponsors. Building strong relationships with the global study team and investigators, you will conduct monitoring on complex clinical trials for different pharma companies, ensuring adherence to good clinical practices and study protocols.

This role, supported by strategic site relationship managers, offers an excellent opportunity to embed yourself in the wider clinical operations team and contribute to groundbreaking new medicine development.

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 according to regulatory requirements, i.e., GCP and ICH guidelines.
• Managing progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolution.
• Collaborating with study site experts and client representatives.

Qualifications:

• University Degree in life sciences or a related scientific discipline, or apprenticeship in healthcare.
• Minimum of one year of on-site monitoring experience or an equivalent combination of education, training, and experience.
• Knowledge of clinical research regulatory requirements, including GCP and ICH guidelines.
• Strong communication skills, attention to detail, and ability to work in a fast-paced environment.
• Proficiency in German and English.
• Flexibility for business travel up to 60% of working time.
• Driver’s license class B.

What you can expect:

• Resources supporting your career growth.
• Supportive leadership with flexible work schedules.
• Programs to enhance your therapeutic knowledge.
• Dynamic work environments offering new experiences.
• Home-office options, company car or allowance, insurance, pension, and more.

Whatever your career goals, we are here to help you achieve them!

We invite you to join IQVIA.

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

#CRAFSAJD

IQVIA is a leading global provider of analytics, technology solutions, and clinical research services to the life sciences industry. We aim to push the boundaries of human and data science to make a significant impact—helping our clients create a healthier world. Learn more at our website.