Senior Clinical Research Specialist
21 uur geleden
We are seeking a highly skilled and experienced Clinical Research Coordinator to join our team in Zwolle.
This is a freelance position, requiring 24-40 hours of work per week for approximately 12-17 months. The successful candidate will be responsible for supporting a clinical research study and ensuring compliance with health and safety policies under the direction of the Principal Investigator.
About the Role:- Maintain accurate and up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents.
- Perform ECGs and vital sign measurements as required.
- Coordinate logistical activities for study procedures according to the study protocol.
- Ensure data quality by conducting regular checks and resolving queries efficiently.
- Assist with study enrollment by recruiting, screening, and orienting volunteers according to the study protocol.
- Manage study drug inventory and ensure adherence to site standard operating procedures.
- Collaborate with the study monitor to resolve any issues that may arise during the study.
- Bachelor's degree in life sciences or equivalent experience in a clinical environment or medical setting.
- Excellent knowledge of clinical trials, including departmental, protocol, and study-specific operating procedures, consent forms, and study schedules.
- Familiarity with medical terminology.
- Strong IT skills, including proficiency in MS Windows and Office applications such as Access, Outlook, Excel, and Word.
- Exceptional interpersonal skills, enabling effective working relationships with colleagues, managers, and clients.
- Good organizational skills, with attention to detail.
- Fluent Dutch language skills, with good English language skills.
The estimated salary for this role is €45,000 - €65,000 per year, depending on experience and qualifications.
Please note that we cannot disclose the company's budget for this role.
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