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- Aufgaben: Join us as a Clinical Research Associate, ensuring oncology trials run smoothly and safely.
- Arbeitgeber: Proclinical is a leading company in clinical research, dedicated to advancing healthcare.
- Mitarbeitervorteile: Enjoy flexible work options, travel opportunities, and a chance to make a real impact.
- Warum dieser Job: Be part of groundbreaking oncology research while building professional relationships and enhancing your skills.
- Gewünschte Qualifikationen: A degree in a relevant field and familiarity with ICH/GCP guidelines are essential.
- Andere Informationen: Fluency in English and German is required; travel is part of the role.
Das voraussichtliche Gehalt liegt zwischen 36000 - 60000 € pro Jahr.
Proclinical is seeking a Clinical Research Associate to ensure clinical study sites adhere to protocols and guidelines, focusing on oncology trials. The successful candidate will be crucial in facilitating patient recruitment and maintaining compliance with regulatory standards.
Responsibilities:
- Ensure clinical trials are conducted in compliance with protocols, SOPs, and ICH/GCP guidelines.
- Conduct site initiation, monitoring, and close-out visits across various study phases.
- Develop and implement patient recruitment strategies at the site level.
- Identify and address site needs and issues, providing solutions to facilitate trial processes.
- Ensure accurate safety reporting and track adverse events.
- Assist in audit preparations and resolve findings.
- Build and maintain professional relationships with investigators and site staff.
Key Skills and Requirements:
- Degree in a relevant field (BA/BS/BSc or similar).
- Familiarity with ICH/GCP guidelines and local codes of practice.
- Experience or training as a Clinical Research Associate.
- Proficiency in English and German.
- Willingness to travel.
- Proficient in common software packages.
- Strong flexibility and teamwork skills.
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Clinical Research Associate - East Germany Arbeitgeber: Proclinical Group
Kontaktperson:
Proclinical Group HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Clinical Research Associate - East Germany
✨Tip Number 1
Make sure to familiarize yourself with the latest ICH/GCP guidelines and local regulations. This knowledge will not only help you during the interview but also demonstrate your commitment to compliance in clinical trials.
✨Tip Number 2
Network with professionals in the oncology field. Attend relevant conferences or webinars to meet potential colleagues and learn about the latest trends in clinical research, which can give you an edge in discussions during the hiring process.
✨Tip Number 3
Prepare to discuss specific patient recruitment strategies you've implemented in the past. Highlighting your experience in overcoming challenges related to patient enrollment can set you apart from other candidates.
✨Tip Number 4
Showcase your flexibility and teamwork skills by providing examples of how you've successfully collaborated with site staff and investigators in previous roles. This will illustrate your ability to build strong professional relationships, which is crucial for this position.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Clinical Research Associate - East Germany
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 required skills, especially those related to oncology trials and compliance with ICH/GCP guidelines.
Tailor Your CV: Customize your CV to highlight relevant experience and skills that align with the job requirements. Emphasize any previous roles in clinical research, particularly those involving patient recruitment and compliance monitoring.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your understanding of the oncology field. Mention specific experiences that demonstrate your ability to meet the responsibilities outlined in the job description.
Highlight Language Proficiency: Since proficiency in both English and German is required, make sure to clearly state your language skills in your application. If you have any certifications or relevant experiences that showcase your language abilities, include them.
Wie du dich auf ein Vorstellungsgespräch bei Proclinical Group vorbereitest
✨Know Your Protocols
Make sure you are well-versed in ICH/GCP guidelines and the specific protocols related to oncology trials. This knowledge will demonstrate your commitment to compliance and your understanding of the clinical research landscape.
✨Showcase Your Recruitment Strategies
Be prepared to discuss your experience or ideas for patient recruitment strategies. Highlight any successful methods you've implemented in the past, as this is a key responsibility of the role.
✨Emphasize Teamwork and Flexibility
Since the role requires strong teamwork skills, share examples of how you've successfully collaborated with others in previous positions. Also, express your willingness to adapt to changing circumstances, especially when it comes to site needs.
✨Prepare for Compliance Questions
Expect questions about how you would handle compliance issues or adverse events. Think through scenarios where you had to ensure safety reporting and how you resolved findings during audits.
