Senior Clinical Research Associate

🕒 August 18

🌐 Belgium, Germany, +1 more countries – Remote

🇧🇪 Belgium – Remote 🇩🇪 Germany – Remote 🇳🇱 Netherlands – Remote

💵 €60.3k - €92k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 22%

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BD

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1897

🏥 Healthcare

🏭 Manufacturing

⚕️ Healthcare Insurance

💰 $24M Grant on 2020-07

Healthcare • Manufacturing • Healthcare Insurance

BD (Becton, Dickinson and Company) is a global medical technology company dedicated to advancing the world of health. It focuses on developing innovative technologies, services, and solutions to improve safety and efficiency in healthcare. BD offers a wide range of products including medication management solutions, surgical solutions, cervical cancer screening, drug delivery systems, and laboratory services. The company is also involved in infection risk management and provides advanced clinical insights to enhance patient outcomes. With a commitment to global health sustainability and social investing, BD is a leader in healthcare technology and services worldwide.

📋 Description

• Lead site management activities from site qualification and initiation through study close-out • Build and maintain relationships with investigators, study coordinators, and site personnel • Conduct on-site and remote monitoring visits according to study protocols, GCP, ISO 14155, and applicable regulations • Drive site activation, patient enrollment, retention, and overall site performance • Identify risks and operational challenges and implement mitigation strategies • Ensure clinical data accuracy, completeness, quality, and protocol compliance • Review and contribute to essential clinical study documentation • Support internal and external audits and inspections and resolve findings • Partner with Clinical Project Managers and cross-functional stakeholders • Contribute to process improvements, best-practice sharing, and clinical monitoring tools and resources

🎯 Requirements

• Bachelor's degree in Life Sciences or a related field, or an equivalent combination of education and experience • Minimum of 5 years of experience in clinical research within the medical device, pharmaceutical, or biotechnology industry • Minimum of 4 years of experience in site management, monitoring, and/or clinical project management • Strong knowledge of domestic and international clinical research regulations, ICH-GCP, ISO 14155, and industry best practices • Familiarity with eTMF, CTMS, and CDMS platforms • Willingness and ability to travel up to 60% or more during peak study periods • Experience supporting clinical studies in peripheral vascular disease, end-stage kidney disease, and/or oncology • Previous experience in medical device clinical research • Proficiency with Veeva Vault CTMS, CDMS, and eTMF • Professional certification through organizations such as ACRP, SOCRA, or equivalent • Fluent in Dutch, English, and German

🏖️ Benefits

• Comprehensive Total Rewards program • Reward and recognition opportunities • Competitive compensation and benefits programs • Learning, growth, and development opportunities • Face-to-face collaboration culture • Equal opportunity employment