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Oncology Study Coordinator
2 weeks ago
The Clinical Trial Coordinator will be responsible for conducting start-up activities, including feasibility assessments, site identification, and regulatory package reviews.
They will also be responsible for facilitating screenings, enrolment visits, and patient eligibility assessments, as well as managing adverse events and concomitant medication.
Additionally, the coordinator will be responsible for entering information on eCRF systems, responding to queries, and managing trial invoicing and payments.
The successful candidate will have excellent time management and organizational skills, as well as the ability to work effectively in a matrix and virtual team environment.
