This is an exciting opportunity with candidates to start as soon as possible!
The Study Coordinator must have minimum 1 year clinical research experience as they need an individual who can work independently as well as part of a team. Day to day responsibilities will involve Prepare Patient Visits (Lab, Vital Signs, Patient Questionnaires, Document Patient Visits, Data Entry and Query Resolution, Configure tablets for patients questionnaires, Train patients in tablet use, Oversight of lab sampling process, Shipment of lab samples (IATA Certificate required), Communicate with CRAs, e.G. on queries and follow-ups, Upload of CTs/MRTs and Maintenance of Investigator Site Files.
Must have experience:
* Having Worked as a Clinical Research Coordinator
* Having Worked in a Study Team
* Knowledge of Oncology Terminology, e.G. Melanoma Studies
* Having Worked on Oncology Studies, preferably including Melanoma Studies
* Having Worked with Medidata RAVE (eCRF/EDC)
* Having Worked with Interactive Voice/Web Response Systems, preferably Clinphone