Clinical Research Professional
1 week geleden
We are seeking a highly skilled Clinical Research Professional to support our team in Amsterdam.
The ideal candidate will have a strong background in life sciences and relevant work experience in a clinical environment or medical setting. They will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies.
This freelance role is estimated to last approximately 12-17 months, with an expected workload of 16-40 hours per week. The successful candidate will be involved in various administrative tasks to support the clinical trial team, including:
- Maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
- Performing ECGs and taking vital signs
- Planning and coordinating logistical activities for study procedures according to the study protocol
- Data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
- Assisting in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
- Correcting custody of study drug according to site standard operating procedures
- Coordinating with study monitors on study issues and effectively responding to monitor-initiated questions
As a key member of the site team, you will be responsible for ensuring the smooth running of the clinical trial. We are looking for candidates with:
- A BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting
- Qualified and competent in ECG and vital signs
- Good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol, and study-specific operating procedures, consent forms, and study schedules
- Basic knowledge of medical terminology
- Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
- Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers, and clients
- Good organizational skills with the ability to pay close attention to detail
- Fluent Dutch with good English language skills
This is a challenging yet rewarding opportunity for individuals who are passionate about clinical research and have excellent communication and organizational skills. If you meet the required qualifications, we encourage you to apply.
The estimated annual salary for this position is around €50,000-€70,000 depending on experience and qualifications. IQVIA offers a competitive compensation package and opportunities for professional growth and development.
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