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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 40-60% 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: PharmiWeb.jobs: Global Life Science Jobs
Kontaktperson:
PharmiWeb.jobs: Global Life Science Jobs 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. Engaging with them can provide you with insider insights about the company culture and expectations, which can be invaluable during your application process.
✨Tip Number 3
Prepare for potential interview questions by reviewing common scenarios faced by Clinical Research Associates. Think about how you would handle site monitoring challenges or regulatory compliance issues, as these are key aspects of the job.
✨Tip Number 4
Highlight your flexibility and willingness to travel in conversations or interviews. Since the role requires travel up to 40-60% of the time, showing that you are adaptable and ready for this aspect can set you apart from other candidates.
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: Make sure you fully understand the responsibilities and qualifications required for the Clinical Research Associate position. Tailor your application to highlight relevant experiences that align with these requirements.
Craft a Strong Motivation Letter: In your motivation letter, express your passion for clinical research and how your background in life sciences or healthcare makes you a suitable candidate. Mention specific experiences that demonstrate your skills in site monitoring and regulatory compliance.
Highlight Relevant Experience: When updating your CV, emphasize any previous on-site monitoring experience and your knowledge of GCP and ICH guidelines. Use bullet points to clearly outline your achievements and responsibilities in past roles.
Proofread Your Application: Before submitting your application, carefully proofread your CV, motivation letter, and any additional documents. Ensure that your German language skills are reflected accurately, especially since fluency at C1 level is required.
Wie du dich auf ein Vorstellungsgespräch bei PharmiWeb.jobs: Global Life Science Jobs 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 Clearly in Both Languages
Since fluency in German and a good command of English are required, practice articulating your thoughts clearly in both languages. This will show your ability to communicate effectively with diverse teams and clients.
✨Prepare for Questions on Flexibility and Travel
Be ready to discuss your flexibility regarding travel, as the role requires up to 40-60% travel time. Share any relevant experiences that showcase your adaptability and willingness to meet the demands of the job.
