CRA II Netherlands

Location: Home-based, Netherlands

Therapeutic Areas: Oncology & Cardiology

Company: Leading Global CRO

Job Type: Full-time, Permanent

Language Requirement: Fluent in Dutch and English

Role Overview:

We are currently recruiting for a Clinical Research Associate (CRA) to join this dynamic and forward-thinking team. This is a home-based position in the Netherlands that offers an exciting opportunity to work with cutting-edge trials in oncology and cardiology. The ideal candidate will have a minimum of 3 years of monitoring experience as a CRA and be fluent in both Dutch and English.

Our client is a leading global Contract Research Organization (CRO) renowned for its comprehensive clinical trial services. With a focus on excellence, they work across various therapeutic areas, including oncology and cardiology. The company offers outstanding growth and promotion opportunities, and it has a single sponsor-dedicated model, ensuring a unique and highly specialised working environment.

Key Responsibilities:

• Site Management: Conduct and manage monitoring visits, ensuring adherence to the clinical trial protocol, regulatory requirements.
• Patient Recruitment & Data Collection: Oversee the recruitment process for patients, ensuring data is accurately collected and managed throughout the study.
• Collaboration: Serve as the main point of contact between the clinical trial site and the sponsor, ensuring smooth communication and timely issue resolution.
• Regulatory Compliance: Ensure clinical trials are conducted in compliance with regulatory requirements and sponsor expectations, ensuring proper documentation and adherence to timelines.
• Monitoring & Reporting: Monitor trial progress, identifying issues early and ensuring that they are addressed promptly to avoid delays or non-compliance.
• Therapeutic Area Expertise: Specialize in oncology and cardiology trials, leveraging your knowledge and expertise to support the delivery of high-quality trials in these areas.

Requirements:

• Experience: Minimum 3 years of clinical monitoring experience. Experience in oncology or cardiology is highly desirable.
• Languages: Fluent in Dutch and English (both written and spoken).
• Education: A degree in a life sciences or related field is preferred.
• Flexibility: The role is home-based, offering flexibility and autonomy in managing your schedule.
• Senior CRA candidates with leadership experience will be considered for more advanced responsibilities.

What’s on Offer:

• Competitive Salary: Attractive salary package and benefits.
• Single Sponsor-Dedicated: Work closely with a leading sponsor, allowing for long-term, focused relationships and a deep understanding of the trials you are managing.
• Career Growth: The company offers multiple promotion opportunities, with the potential for career advancement as you gain experience and expertise.
• Home-Based Flexibility: The role is primarily home-based, allowing for a great work-life balance.

Why Join Us:

This is a fantastic opportunity for Clinical Research Associates at various stages of their careers to advance with a global leader in the CRO industry. Specialising in oncology and cardiology, you will contribute to high-impact clinical trials that aim to improve patient outcomes. The company prioritises career progression, offering a collaborative and supportive environment with ample opportunities for professional growth.