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- Aufgaben: Join our team as a Clinical Research Associate, ensuring successful clinical trials in oncology and rare diseases.
- Arbeitgeber: Scienta is a global leader in clinical research, dedicated to improving patient outcomes through innovation.
- Mitarbeitervorteile: Enjoy a supportive work environment with a focus on professional development and work-life balance.
- Warum dieser Job: Be part of a dynamic team making a real impact in healthcare while collaborating with passionate professionals.
- Gewünschte Qualifikationen: You need a Bachelor's degree and at least 2 years of CRA experience, especially in oncology.
- Andere Informationen: This role requires travel within Germany for site visits, approximately five times a month.
Das voraussichtliche Gehalt liegt zwischen 42000 - 84000 € pro Jahr.
Direct message the job poster from Scienta
Building global clinical operations teams across the life science industry | Scienta
Clinical Research Associate II / III
This role is open to candidates with a minimum of two years experience as a CRA in Germany.
Location: Frankfurt or Cologne, Germany
The Company
We are a global Clinical Research Organization (CRO) renowned for delivering high-quality clinical trial services across diverse therapeutic areas, including oncology and rare diseases. Our mission is to improve patient outcomes by driving innovation in clinical research. With a strong emphasis on professional development, collaboration, and work-life balance, we offer a dynamic and supportive environment for our team members.
The Role
We are seeking an experienced Clinical Research Associate (CRA) II or III to join our team in Germany. Based out of Frankfurt or Cologne, you will play a pivotal role in ensuring the successful conduct of clinical trials in oncology and rare diseases across Germany. This role involves approximately five site visits per month and requires a dedicated professional who thrives in a fast-paced, collaborative setting.
Main Responsibilities
- Conduct site qualification, initiation, monitoring, and close-out visits to ensure compliance with protocols, GCP, and regulatory requirements.
- Serve as the primary point of contact for assigned study sites, fostering strong site relationships.
- Perform source document verification and data monitoring to ensure data accuracy and protocol adherence.
- Collaborate with site staff to resolve data queries, protocol deviations, and other site-related issues.
- Ensure timely reporting of adverse events and serious adverse events to the appropriate stakeholders.
- Prepare and submit detailed visit reports and follow-up correspondence in a timely manner.
- Assist in site staff training to ensure proper trial execution.
- Participate in investigator meetings, providing site-related insights and updates.
Requirements
- Bachelor\’s degree in Life Sciences, Nursing, or a related field.
- Minimum of 2 years experience as a CRA in clinical trials, with a focus on oncology and rare diseases.
- Comprehensive knowledge of ICH-GCP, regulatory requirements, and clinical trial processes.
- Proven ability to perform on-site monitoring and manage multiple sites effectively.
- Strong organizational, problem-solving, and communication skills.
- Proficiency in German and English, both written and spoken.
- Willingness to travel within Germany for site visits (approximately 5 per month).
- A valid driver\’s license and access to a reliable vehicle.
How To Apply
Apply here for a confidential discussion about this opportunity.
Seniority level
Associate
Employment type
Full-time
Job function
Research and Science
Industries
Staffing and Recruiting, Biotechnology Research, and Pharmaceutical Manufacturing
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Clinical Research Associate Arbeitgeber: Scienta
Kontaktperson:
Scienta HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Clinical Research Associate
✨Tip Number 1
Nutze LinkedIn, um dich mit Fachleuten aus der klinischen Forschung zu vernetzen. Suche nach Personen, die bei Scienta arbeiten, und sende ihnen eine direkte Nachricht, um mehr über die Unternehmenskultur und die spezifischen Anforderungen der Position zu erfahren.
✨Tip Number 2
Informiere dich über aktuelle Trends und Entwicklungen in der Onkologie und bei seltenen Krankheiten. Zeige in Gesprächen oder Interviews, dass du über das nötige Wissen verfügst, um in diesem spezialisierten Bereich erfolgreich zu sein.
✨Tip Number 3
Bereite dich darauf vor, konkrete Beispiele aus deiner bisherigen CRA-Erfahrung zu teilen, insbesondere solche, die deine Fähigkeiten im Umgang mit mehreren Standorten und die Einhaltung von GCP-Richtlinien demonstrieren.
✨Tip Number 4
Zeige deine Reisebereitschaft und Flexibilität, indem du in deinem Gespräch betonst, wie wichtig dir die persönliche Interaktion mit den Studienstandorten ist. Dies wird deine Eignung für die Rolle unterstreichen.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Clinical Research Associate
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description for the Clinical Research Associate position. Understand the key responsibilities and requirements, especially the emphasis on oncology and rare diseases.
Highlight Relevant Experience: In your application, emphasize your experience as a CRA, particularly any work related to oncology or rare diseases. Use specific examples to demonstrate your skills in site monitoring and compliance with GCP and regulatory requirements.
Showcase Your Skills: Clearly outline your organizational, problem-solving, and communication skills in your CV and cover letter. Mention your proficiency in both German and English, as this is crucial for the role.
Tailor Your Application: Customize your CV and cover letter to reflect the values and mission of Scienta. Highlight your commitment to improving patient outcomes and your ability to thrive in a collaborative environment.
Wie du dich auf ein Vorstellungsgespräch bei Scienta vorbereitest
✨Showcase Your Experience
Make sure to highlight your previous experience as a Clinical Research Associate, especially in oncology and rare diseases. Be prepared to discuss specific trials you've worked on and the impact of your contributions.
✨Demonstrate Knowledge of GCP and Regulations
Familiarize yourself with ICH-GCP guidelines and relevant regulatory requirements. During the interview, be ready to explain how you ensure compliance during site visits and monitoring activities.
✨Emphasize Communication Skills
As a CRA, strong communication is key. Prepare examples of how you've effectively communicated with site staff and resolved issues. This will show your ability to foster strong relationships and collaborate effectively.
✨Prepare for Site Visit Scenarios
Anticipate questions about how you would handle various site visit scenarios. Think about challenges you've faced in the past and how you overcame them, as this will demonstrate your problem-solving skills.
