Are you interested in a career in Clinical Research? This may be the job for you. The Oncology Clinical Trials Data Coordinator will work hand in hand with the Clinical Research Coordinators, the Regulatory Coordinator and the Director of Clinical Research. The team addresses regulatory and safety support services including clinical trial communication and document distribution, critical document collection, safety reporting, translation of informed consent documents and communication with sponsor representatives. It is a fast paced environment. No two days are the same.
Duties and Responsibilities of the the Oncology Clinical Trials Data Coordinator:
1)Person will be responsible for the completeness and consistency of the data collection necessary for the ongoing trials by completing the case report forms.
2) The data that will be collected are the adverse events, concomitant medications, disease progress, and demographics of the patients.
3) Person will be entering data in Electronic Data Capture for various trials, creating source documentation, and answering queries.
4) Work side by side the research coordinator to help execute clinical tasks including central labs, drug accountability, radiology requests, training of staff for protocol amendments
Education, Skills and Experience Required for the Oncology Clinical Trials Data Coordinator:
Job Type: Full-time
Salary: $36,000.00 to $42,000.00 /year
This Company Describes Its Culture as: