Clinical Research Associate
2 semanas atrás
At our organization, we prioritize career development and progression; engaged line management; technical training; recognition and rewards.
As a Clinical Research Associate I, you will play a key role in the site activation process for clinical trials. Your primary responsibility will be to manage and coordinate all activities necessary to initiate a trial at a research site. This includes preparing and managing trial-related documents, conducting site feasibility assessments, and ensuring compliance with regulations and company policies.
- You will work closely with cross-functional teams, including project managers, data managers, and biostatisticians, to ensure seamless execution of clinical trials.
- Develop and maintain relationships with study investigators, site staff, and other stakeholders to facilitate effective communication and collaboration.
- Conduct site initiation visits (SIVs) and monitoring visits to assess the site's preparedness and ability to conduct the trial in accordance with Good Clinical Practice (GCP) guidelines.
The ideal candidate will have a strong understanding of clinical trial management principles, excellent communication and interpersonal skills, and the ability to work effectively in a fast-paced environment.
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