Job Title: Oncology Clinical Research Associate — Ireland Monitoring
We are seeking a highly skilled and experienced professional to support Oncology studies as a Clinical Research Associate.
This role is an excellent opportunity for individuals who wish to make a difference in the healthcare industry while developing their skills in clinical research.
1. Monitoring sites to ensure compliance with protocols and regulations, managing study-related documentation, and supporting the efficient conduct of clinical trials.
2. Coordinating site initiations, monitoring visits, close-out activities and ensuring timely submission of reports to sponsors
3. The ideal candidate will have experience working within regulatory frameworks such as ICH GCP guidelines
Candidates should hold relevant qualifications or experience preferably in life sciences. The ability to work independently and effectively prioritize multiple tasks under pressure is essential. Additionally having knowledge of Good Clinical Practice (GCP) principles would be beneficial but not required.
Knowledge Required:
* Bachelor's degree in Life Sciences or equivalent qualification
* Experience of working within regulatory frameworks
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The ideal applicant will have effective communication skills strong attention to detail reliability flexibility adaptability best practices punctuality accountability coordination [time management]. [go team] physical stamina travel requirement co worker high level customer service understanding patient involvement Compliance Risk Managements information governance Administrative procedures policy implementation data protection drug safety benefits compliance deliverables responsibilities partnering other complimentary discipline positive influence leadership competent continuity analytical collected upon enrollment assignment.