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Solliciteren



Research Associate


We are looking for an experienced Senior CRA & Country Head to strengthen our clinical operations in Belgium! Higher education – preferred qualification in nursing, life sciences or medical sciences Profound knowledge of clinical research processes and medical terminology Expert knowledge of ICH GCP, and international and local regulatory requirements English language proficiency of minimum level C1 (ref. CEFR) – fluent in written and spoken English Ensure that Clinical Trial is conducted, recorded, and reported in accordance with all applicable international and local regulations and guidelines, good practices, SOPs and Clinical Trial Protocol. Ensuring data quality and integrity meet acceptable clinical standards and the rights and safety of patients involved in a study are protected. Conduct remote and on-site visits to assess protocol and regulatory compliance and manage required documentation. Develop collaborative relationships with investigational sites, act as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects rights, well-being, and data reliability; Apart from general CRA responsibilities, you would mentor and supervise less experienced colleagues and ensure their professional development and quality of their performance. As country head you will also be responsible for the overall functioning of the local office , including its set-up, compliance with legal requirements, facility, technical and human resources, cooperation with headquarters and and everyday local operations. Flexible working hours and home-based working option Great work-life balance (You will not be overwhelmed with projects as we believe in quality over quantity) Career growth and development opportunities in a continuous learning culture Friendly environment in a privately owned international company

Solliciteren