Description of job position
- Conducting monitoring visits to clinical trial sites to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP).
- Reviewing and verifying study documentation including informed consent forms, source documents, and case report forms.
- Collaborating with site staff to facilitate the smooth execution of clinical trials.
- Providing training and support to site personnel on study protocols and procedures.
- Identifying and resolving issues related to study conduct and data integrity.
- Collecting and reporting adverse events and serious adverse events in accordance with regulatory guidelines.
- Maintaining accurate and timely records of monitoring activities and findings.
- Assisting in the preparation of study-related materials, including monitoring plans and reports.
- Ensuring proper storage and handling of investigational products.
- Participating in project team meetings and contributing to study progress discussions.
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Position Clinical Research Associate - Medicine & Social Care in the labour market
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the job position takes
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