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- Aufgaben: Join us as a Clinical Research Associate, managing site visits and ensuring compliance with regulations.
- Arbeitgeber: IQVIA is a global leader in clinical research services, enhancing healthcare through innovative solutions.
- Mitarbeitervorteile: Enjoy flexible work schedules, home-office options, and resources for career growth.
- Warum dieser Job: Gain hands-on experience in diverse therapeutic areas while receiving world-class training and mentorship.
- Gewünschte Qualifikationen: A degree in life sciences or healthcare, plus at least one year of monitoring experience required.
- Andere Informationen: Fluency in German (C1) and English is essential; travel up to 60% may be needed.
Das voraussichtliche Gehalt liegt zwischen 36000 - 60000 € pro Jahr.
When you join IQVIA as a sponsor-dedicated Clinical Research Associate / CRA (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 one year 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
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Clinical Research Associate (m/w/d), Single Sponsor Arbeitgeber: IQVIA, Inc.
Kontaktperson:
IQVIA, Inc. HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Clinical Research Associate (m/w/d), Single Sponsor
✨Tip Number 1
Make sure to familiarize yourself with the specific therapeutic areas that IQVIA focuses on. This knowledge will not only help you during interviews but also demonstrate your genuine interest in the role and the company.
✨Tip Number 2
Network with current or former Clinical Research Associates at IQVIA through platforms like LinkedIn. They can provide valuable insights into the company culture and expectations, which can be beneficial for your application.
✨Tip Number 3
Prepare to discuss your previous monitoring experiences in detail. Be ready to share specific examples of how you've ensured compliance with GCP and ICH guidelines, as this will showcase your expertise and readiness for the role.
✨Tip Number 4
Highlight your flexibility and willingness to travel in your conversations. Since the role requires up to 40-60% travel, showing that you're adaptable and ready for this aspect will make you a more attractive candidate.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Clinical Research Associate (m/w/d), Single Sponsor
Tipps für deine Bewerbung 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and qualifications required for the Clinical Research Associate position. Familiarize yourself with terms like Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Tailor Your CV: Customize your CV to highlight relevant experience in clinical research and monitoring. Emphasize your educational background in life sciences and any specific projects or roles that demonstrate your expertise in the field.
Craft a Compelling Motivation Letter: Write a motivation letter that clearly articulates your passion for clinical research and why you want to work with IQVIA. Mention your understanding of the company's mission and how your skills align with their goals.
Prepare Supporting Documents: Gather all necessary documents such as certificates, reference letters, and proof of language proficiency. Ensure these documents are up-to-date and relevant to the position you are applying for.
Wie du dich auf ein Vorstellungsgespräch bei IQVIA, Inc. vorbereitest
✨Understand GCP and ICH Guidelines
Make sure you have a solid understanding of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Be prepared to discuss how these regulations impact your work as a Clinical Research Associate.
✨Showcase Your Monitoring Experience
Highlight your previous on-site monitoring experience during the interview. Provide specific examples of how you've managed site selection, initiation, and monitoring visits to demonstrate your expertise.
✨Communicate Effectively
Since strong communication skills are essential for this role, practice articulating your thoughts clearly and concisely. Be ready to discuss how you collaborate with study site experts and client representatives.
✨Demonstrate Flexibility and Adaptability
Be prepared to talk about your flexibility in terms of travel and adapting to different therapeutic areas. Share experiences where you've successfully adjusted to new challenges or environments in your previous roles.
