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

TN Germany; Frankfurt; Vor Ort; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

Join a leading global contract research organization as a Senior Clinical Research Associate in Frankfurt. This role offers career growth and professional development with responsibilities including site monitoring and regulatory compliance. Enjoy a supportive environment with flexible work options and resources for career advancement.

Leistungen

Home-office

Company car

Accident insurance

Qualifikationen

• Minimum of four years of on-site monitoring experience.
• Fluency in German on at least C1 level and a good command of English.

Aufgaben

• Performing site selection, initiation, monitoring and close-out visits.
• Evaluating the quality and integrity of site practices in accordance with regulatory requirements.

Kenntnisse

Communication

Attention to Detail

Ausbildung

University Degree in Life Science

Apprenticeship in Health Care

Jobbeschreibung

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

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Client:

IQVIA

Location:

Frankfurt, Germany

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

6c103470cfa7

Job Views:

1

Posted:

13.05.2025

Expiry Date:

27.06.2025

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Job Description:

Join IQVIA as a Senior Clinical Research Associate / Sr CRA (m/w/d) home-based throughout Germany in our single sponsor department , and advance your career in clinical research. 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)
• Mentoring of less experienced team members, support 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 four years of on-site monitoring experience alternatively an equivalent combination of education, training and 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.

#CRASDAJD

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at