🔎 Clinical Performance Studies Expert

Thuiswerken30+ dagen geleden

Thuiswerken

Over de functie

QbD Group is seeking a Clinical Performance Studies Expert to organize and execute clinical performance studies. You will develop study protocols, analyze complex data, and ensure compliance with international regulations like IVDR and ISO 20916.

Wat ga je doen

Organize and execute clinical performance studies including protocol development, monitoring, and reporting
Develop study protocols and project plans aligned with objectives, budget, and regulations
Analyze complex clinical performance data and draft study documentation
Ensure compliance with international regulations like IVDR and ISO 20916
Collaborate with internal teams, customers, and clinical sites
Provide training to study sites and conduct monitoring activities

Wat je meebrengt

Bachelor's, Master's, or PhD in a relevant scientific discipline
Minimum 3 years of experience with IVD development activities
Good knowledge of IVD clinical performance study design and regulatory requirements
Fluent in English
Attention to detail in study protocols, data analysis, and report writing
Analytical skills with experience in statistical software tools

Mooi meegenomen

Expertise in infectious diseases or oncology
Knowledge of Common Specifications
Additional languages

Wat je krijgt

Attractive and competitive salary package tailored to individual needs
Sustainable career with job security
Continuous learning and development opportunities
Part of a global award-winning company

Over QbD Group

QbD Group is a global award-winning company.

Samenvatting door Personeel.com. De volledige vacaturetekst en het sollicitatieformulier staan op de website van QbD Group (careers.qbdgroup.com); met Solliciteer ga je er direct heen.

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