Auf einen Blick
- Aufgaben: Manage global clinical trials and ensure compliance across Europe.
- Arbeitgeber: Join a pioneering MedTech company revolutionizing heart valve therapy.
- Mitarbeitervorteile: Enjoy competitive salary, bonuses, stock options, and career development opportunities.
- Warum dieser Job: Make a significant impact in healthcare while working in a dynamic, innovative culture.
- Gewünschte Qualifikationen: Bachelor's degree with 5+ years in clinical trial monitoring; medical device experience preferred.
- Andere Informationen: Up to 50% travel required; fluency in multiple EU languages is a plus.
Das voraussichtliche Gehalt liegt zwischen 48000 - 72000 € pro Jahr.
Job Description Sr. Clinical Research Associate The Company The Company is a pioneering MedTech company developing the first-in-class structural heart valve. We seek a passionate Sr. Clinical Research Associate to join our growing team. You’ll play a pivotal role in managing a global pivotal trial across Europe, ensuring its success and advancing this groundbreaking therapy. About The Company The Company is a global company with offices in US, Switzerland, and Australia. We foster a collaborative and dynamic work environment with a culture of innovation and excellence. Join us and make a significant impact on the healthcare industry! The Role You’ll oversee daily operations at investigational sites across Europe for our pivotal trial. This includes ensuring compliance with international guidelines, local regulations, and company policies. You’ll also manage vendor activities, oversee data collection and cleaning, and potentially conduct site monitoring visits. Key Responsibilities Oversee vendor activities and participate in study start-up and conduct. Lead investigations into discrepancies in study documentation. Conduct reviews of documentation for internal and external audits. Train site personnel and vendors on study protocols and regulatory requirements. Assess data documentation, reports, and records for consistency and compliance. Verify trial data and ensure proper regulatory documentation is maintained. Qualifications Bachelor’s degree in a relevant field with 5+ years of clinical trial monitoring experience. Medical device experience, with strong preference for Class III cardiovascular devices. Experience with site- and sponsor-level audits. Excellent communication, presentation, interpersonal, and analytical skills. Experience working with CROs, core labs, and external vendors. Proven problem-solving, critical thinking, and attention to detail. Expertise in MS Office suite and Adobe applications. Experience with Electronic Data Capture Systems (EDC) required. Thorough knowledge of GCP and working knowledge of relevant regulations. Clinical research certification preferred. Up to 50% travel across Europe required. Fluency in English. Fluency in French and German a plus, other EU languages a benefit. Competitive Benefits Package Competitive salary, performance-based bonuses, and stock options. Comprehensive benefits package. Career development opportunities in a growing and innovative company. Ready to make a difference? We are searching for a highly motivated and results-oriented individual to join our team. If you are passionate about advancing healthcare and eager to contribute to a groundbreaking therapy, we encourage you to apply! Please note: Due to privacy restrictions, we are unable to disclose the specific location of this role. However, qualified candidates with fluency in additional European languages are strongly encouraged to apply. #LI-OG1
Senior CRA Arbeitgeber: Pharmiweb
Kontaktperson:
Pharmiweb HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Senior CRA
✨Tip Number 1
Make sure to highlight your experience with Class III cardiovascular devices in your conversations. This is a key requirement for the role, and demonstrating your expertise can set you apart from other candidates.
✨Tip Number 2
Network with professionals in the MedTech industry, especially those who have experience in clinical trials. Engaging with them can provide valuable insights and potentially lead to referrals within our company.
✨Tip Number 3
Familiarize yourself with the latest GCP guidelines and relevant regulations. Being well-versed in these areas will not only boost your confidence but also demonstrate your commitment to compliance during interviews.
✨Tip Number 4
If you speak additional European languages, be sure to mention this in discussions. Fluency in languages like French or German can be a significant advantage and shows your ability to work effectively across diverse teams.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Senior CRA
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure you fully understand the responsibilities and qualifications required for the Senior Clinical Research Associate position. Tailor your application to highlight relevant experiences that align with the job description.
Highlight Relevant Experience: Emphasize your clinical trial monitoring experience, especially with Class III cardiovascular devices. Provide specific examples of your past roles and how they relate to the key responsibilities mentioned in the job description.
Showcase Your Skills: Clearly outline your communication, analytical, and problem-solving skills in your CV and cover letter. Mention your proficiency with MS Office, Adobe applications, and Electronic Data Capture Systems (EDC) as these are crucial for the role.
Language Proficiency: If you are fluent in French, German, or any other EU languages, make sure to highlight this in your application. This can set you apart from other candidates and is a significant advantage for the role.
Wie du dich auf ein Vorstellungsgespräch bei Pharmiweb vorbereitest
✨Showcase Your Clinical Trial Experience
Be prepared to discuss your previous experience in clinical trial monitoring, especially with Class III cardiovascular devices. Highlight specific examples where you ensured compliance with international guidelines and local regulations.
✨Demonstrate Problem-Solving Skills
Expect questions that assess your critical thinking and problem-solving abilities. Prepare to share instances where you successfully resolved discrepancies in study documentation or managed vendor activities effectively.
✨Highlight Communication Skills
Since the role requires excellent communication and interpersonal skills, practice articulating your thoughts clearly. Be ready to explain how you've trained site personnel and vendors on study protocols and regulatory requirements.
✨Familiarize Yourself with EDC Systems
As experience with Electronic Data Capture Systems (EDC) is required, brush up on your knowledge of these systems. Be ready to discuss your proficiency with MS Office and Adobe applications as well.