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- Aufgaben: Coordinate patient visits and manage data entry for clinical research.
- Arbeitgeber: Join a leading organization in oncology research based in Mannheim, Germany.
- Mitarbeitervorteile: Enjoy flexible part-time hours and gain valuable experience in the healthcare field.
- Warum dieser Job: Make a real impact in cancer research while developing your skills in a supportive environment.
- Gewünschte Qualifikationen: Knowledge of oncology terminology and experience with Medidata RAVE required.
- Andere Informationen: GCP training certificate must be current (within 1 year).
Job Title: Clinical Research Coordinator – Germany
Location: Mannheim, Germany
Job Type: Part Time Contract
Responsibilities:
- Prepare Patient Visits (Lab, Vital Signs, Patient Questionnaires)
- Document Patient Visits
- Data Entry and Query Resolution
- Configure tablets for patients‘ questionnaires
- Train patients in tablet use
- Oversight of lab sampling process
- Shipment of lab samples (IATA Certificate required)
- Communicate with CRAs, e.g. on queries and follow-ups
- Upload of CTs/MRTs
- Maintenance of Investigator Site Files
Requirements:
- Knowledge of Oncology Terminology, e.g. Melanoma Studies
- Having Worked on Oncology Studies, preferably including Melanoma Studies
- Having Worked with Medidata RAVE (eCRF/EDC)
- Having Worked with Interactive Voice/Web Response Systems, preferably Clinphone
- Preferably having Worked with Laboratory Reporting Systems
- GCP Training Certificate not older than 1 year
#J-18808-Ljbffr
Clinical Research Coordinator - Germany Arbeitgeber: Talentify
Kontaktperson:
Talentify HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Clinical Research Coordinator - Germany
✨Tip Number 1
Familiarize yourself with the latest oncology terminology, especially related to melanoma studies. This knowledge will not only help you in interviews but also demonstrate your commitment to the field.
✨Tip Number 2
If you have experience with Medidata RAVE or similar eCRF/EDC systems, be ready to discuss specific projects where you utilized these tools. Highlighting your hands-on experience can set you apart from other candidates.
✨Tip Number 3
Make sure to mention any relevant GCP training you've completed, especially if it's within the last year. This shows that you are up-to-date with industry standards and practices.
✨Tip Number 4
Prepare to discuss your experience with patient interactions, particularly in training them on technology like tablets for questionnaires. This is a key part of the role, and demonstrating your communication skills will be crucial.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Clinical Research Coordinator - Germany
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description for the Clinical Research Coordinator position. Familiarize yourself with the responsibilities and requirements, especially regarding oncology terminology and experience with Medidata RAVE.
Tailor Your CV: Highlight your relevant experience in oncology studies, particularly any work related to melanoma. Include specific examples of your previous roles that align with the responsibilities listed in the job description.
Craft a Strong Cover Letter: Write a personalized cover letter that emphasizes your passion for clinical research and your familiarity with the tools and processes mentioned, such as lab sampling and patient training. Make sure to connect your skills directly to the job requirements.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors or typos. A polished application reflects your attention to detail, which is crucial in clinical research.
Wie du dich auf ein Vorstellungsgespräch bei Talentify vorbereitest
✨Know Your Oncology Terminology
Make sure you are familiar with key oncology terms, especially those related to melanoma studies. This knowledge will help you communicate effectively and demonstrate your expertise during the interview.
✨Highlight Relevant Experience
Be prepared to discuss your previous work on oncology studies, particularly any experience with melanoma. Share specific examples of your contributions and how they relate to the responsibilities of the Clinical Research Coordinator role.
✨Familiarize Yourself with Medidata RAVE
Since experience with Medidata RAVE is a requirement, brush up on your knowledge of this eCRF/EDC system. Be ready to explain how you've used it in past roles and how it can benefit the team.
✨Prepare for Technical Questions
Expect questions about lab sampling processes and data entry. Review best practices and be ready to discuss how you ensure accuracy and compliance in these areas, as well as your experience with IATA regulations for shipping lab samples.
