5+ years of experience as a Clinical Research Associate.
4-year university degree or RN/BSN in Nursing.
Experience as a CTM managing Oncology trials is required.
Willingness to travel is required.
Responsibilities:
Responsible for managing the research activities at sites participating in Worldwide's clinical research projects, predominantly registries and observational studies.
Involved in all stages of the clinical study including identifying potential sites, conducting study initiation visits, managing site activities during study maintenance, and closing down research activities.
Will ensure compliance with informed consent, reporting safety-related events, and adhering to regulatory requirements.