Senior Clinical Research Associate
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Our client, a global leader in the MedTech industry, is looking for a Senior Clinical Research Associate to support clinical study activities within a MedTech environment.
Is this your next job Read the full description below to find out, and do not hesitate to make an application.
The successful candidate will be responsible for managing clinical activities at study sites conducting clinical studies, while building strong and productive relationships with internal stakeholders and site personnel. This role involves overseeing study site performance, conducting monitoring visits, and ensuring high-quality data collection in compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements.
Responsibilities
- Manage clinical study activities for assigned study sites across one or more clinical projects
- Conduct site monitoring visits and maintain regular communication with site personnel
- Ensure patient safety and wellbeing are maintained throughout the study
- Support the operational execution of clinical trials and ensure collection of high-quality data
- Verify Investigator Site Files are maintained according to regulatory and company requirements
- Support patient recruitment and retention activities
- Identify, escalate, and assist in resolving site-related issues
- Ensure compliance with study protocols, regulatory requirements, and company procedures
- Collaborate with investigators, ethics committees, vendors, and internal stakeholders
- Serve as a reliable source of study site status and progress updates
- Support implementation of new clinical systems and processes
Requirements
- Bachelor's degree in Life Sciences, Biological Sciences, Nursing, Physical Sciences, or a related field
- Minimum 4 years of recent xirbnpk site monitoring experience as a CRA
- Previous clinical research experience
- Medical device or MedTech monitoring experience
- Strong knowledge of GCP and clinical research regulations
- Relevant certifications such as CCRA, RAC, or CDE are desirable
- Strong communication, presentation, and organizational skills
- Ability to manage multiple priorities and deadlines
- Willingness to travel up to 80%
- Fluency in English and Dutch is required
Contract Type
- Freelance / Contract
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