Auf einen Blick
- Aufgaben: Monitor clinical sites and ensure adherence to study protocols in medical device trials.
- Arbeitgeber: Join Edwards Lifesciences, a global leader in patient-focused innovations for heart disease.
- Mitarbeitervorteile: Enjoy flexible hours, remote work, wellness programs, and competitive compensation.
- Warum dieser Job: Make a real impact on patient outcomes while working in a dynamic, inclusive environment.
- Gewünschte Qualifikationen: Bachelor's degree and experience in clinical trials; fluency in German and English required.
- Andere Informationen: Regular travel within Germany and some international travel is expected.
Das voraussichtliche Gehalt liegt zwischen 36000 - 60000 € pro Jahr.
Overview
Innovation starts from the heart. Edwards Lifesciences is the global leader of patient-focused innovations for structural heart disease and critical care monitoring. With millions of patients served in over 100 countries, each team makes a meaningful contribution by improving patient outcomes and discovering lasting solutions for unmet patient needs.
The Clinical Affairs team is looking for an experienced Clinical Research Associate or Senior CRA (depending on experience), to join our team in Germany.
This role will mainly be focused on sites in the western parts of Germany. Suitable locations include Frankfurt, Dusseldorf, Cologne, Bonn, Mainz, Mannheim, and surrounding areas.
This role will be responsible for site monitoring activities to ensure the overall integrity of study implementation and adherence to study protocol at assigned clinical sites. This role will involve working on medical device trials in Cardiology.
How you will make an impact:
- Conduct Clinical Monitoring activities at sites across Germany
- Serve as key contact to assigned clinical sites throughout the study process
- Be accountable for achieving and reporting on agreed clinical milestones
- Support the study team in interactions with Ethics Committees and Competent Authorities
- Participate actively in project team meetings, as required
- Collaborate closely with internal stakeholders to ensure proper project conduct
- Assist in providing site and Edwards personnel training, including preparation/maintenance of study documents, completion of forms, and understanding of examinations/assessments required
- Report site enrollment progress including device accountability and protocol deviations
- Collect completed Case Report Forms (CRF) and supporting documentation
- Process adverse events
- Document procedural case observations for insights into investigating post-procedural events
- Review data, safety reporting, and complaint handling
- Identify and report adverse events and device-related complications in accordance with regulatory and internal requirements
- Develop new improved processes and perform implementation
- Ensure audit readiness for internal, external, and site audits
- Other incidental duties as assigned by management
What you will need:
- Bachelor\’s Degree in a related field, and/or proven record of strong relevant experience
- Previous related medical device and/or clinical experience required
- Previous clinical trial site monitoring experience in Germany within a Medical Device or Pharmaceutical setting
- Experience of different types of monitoring visits and in different study stages
- Quality assurance and regulatory compliance in a clinical research setting
- Driving licence required
- Fluency in both German and English is essential
What else we look for:
- Excellent communication and organizational skills
- Proven expertise in MS Office Suite and ability to operate general office machinery
- Good written and verbal communication skills, presentation, and interpersonal relationship skills including negotiating and relationship management skills
- Good problem-solving and critical thinking skills
- Adherence to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and taking adequate control measures in preventing injuries to themselves and others
- Cardiology and/or medical device study experience desirable
- Driving licence required
This role will require regular travel within Germany (and some international travel).
What is it like to work at Edwards Lifesciences in Germany?
As a global leader in patient-focused medical innovations, we offer rewarding opportunities and exciting challenges in a truly international, dynamic, and friendly work environment.
We are committed to fostering a diverse and inclusive work environment where all employees can grow, personally and professionally. To achieve this, we offer on-the-job development, training opportunities, and the support and guidance provided by dedicated employee groups (the Edwards Network of Women, Edwards Foundation charity team, sustainability activities, and others).
Edwards Lifesciences in Germany also offers the following benefits:
- Competitive Compensation and Benefits package
- Flexible working hours, remote working
- Pension plan
- Insurance Meal Benefits
- Service Awards
- Leave Benefits
- Transportation Benefits
- Employee Stock Purchase Programme
- Employee Assistance Programme
- Comprehensive Wellness Programme including onsite gym, yoga classes, massage, preventive health checks, healthy lifestyle webinars, educational events, charity activities, and much more.
Benefits are regulated by an internal policy which contains the full details regarding the entitlement and conditions for the benefits. Benefits policy and components may vary by location. #J-18808-Ljbffr
Clinical Research Associate / Senior CRA Arbeitgeber: Clinical Research Training Academy
Kontaktperson:
Clinical Research Training Academy HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Clinical Research Associate / Senior CRA
✨Tip Number 1
Make sure to familiarize yourself with the specific medical device trials in Cardiology. Understanding the nuances of these trials will not only help you during interviews but also demonstrate your genuine interest in the role.
✨Tip Number 2
Network with professionals in the clinical research field, especially those who have experience with medical devices. Attend relevant conferences or webinars to connect with potential colleagues and learn more about the industry trends.
✨Tip Number 3
Brush up on your knowledge of regulatory compliance and quality assurance in clinical research settings. Being well-versed in these areas will set you apart as a candidate who understands the importance of adhering to protocols.
✨Tip Number 4
Prepare for potential travel requirements by being flexible and ready to discuss your availability. Highlight any previous experience you have with travel for work, as this is an important aspect of the role.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Clinical Research Associate / Senior CRA
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description for the Clinical Research Associate / Senior CRA position. Understand the key responsibilities and required qualifications, especially the importance of site monitoring activities and experience in medical device trials.
Tailor Your CV: Customize your CV to highlight relevant experience in clinical trial site monitoring, particularly in the medical device or pharmaceutical setting. Emphasize your fluency in both German and English, as well as any specific skills related to cardiology.
Craft a Strong Cover Letter: Write a compelling cover letter that showcases your passion for patient-focused innovations and your understanding of the role. Mention your previous experiences that align with the responsibilities listed, such as conducting clinical monitoring activities and collaborating with internal stakeholders.
Highlight Soft Skills: In your application, emphasize your excellent communication and organizational skills, as well as your problem-solving abilities. These are crucial for the role, especially when interacting with clinical sites and managing relationships with various stakeholders.
Wie du dich auf ein Vorstellungsgespräch bei Clinical Research Training Academy vorbereitest
✨Know Your Clinical Research Basics
Make sure you have a solid understanding of clinical research principles, especially in the context of medical devices. Be prepared to discuss your previous experiences with site monitoring and how they relate to the role.
✨Demonstrate Communication Skills
Since this role requires excellent communication skills, practice articulating your thoughts clearly. Be ready to provide examples of how you've effectively communicated with clinical sites or team members in past projects.
✨Familiarize Yourself with Regulatory Requirements
Brush up on the regulatory compliance aspects of clinical trials in Germany. Understanding the local regulations will show that you are serious about maintaining quality assurance and can navigate the complexities of clinical research.
✨Showcase Problem-Solving Abilities
Prepare to discuss specific challenges you've faced in previous roles and how you resolved them. Highlight your critical thinking skills and your ability to adapt to changing situations, especially in a clinical setting.