Senior Clinical Research Coordinator - Full TimeThe Role:The role is Full Time and is in office.The role includes, but is not limited to the following:Adhere to protocols, ethical and regulatory requirements and GCP guidelines at all times for assigned trialsManage and coordinate participants throughout the studyPreparation, dispensing and administration of the investigatory productStudy-related data entry - source, CRF and site file managementWork with the study team, including ethics, recruitment, coordinators and InvestigatorsAbout you:You must be a team player with excellent communication skills.
Having experience using variety of computer applications, databases and electronic medical records.
Sharing our values of Respect and Responsibility, Collaboration, Quality and Safety,
and Resilience.Other Essential criteria:2–3 years' experience as a Lead Clinical Trial Coordinator.Ability to work independently and as part of a teamExceptional organisational skills and attention to detailTime management skills with the ability to manage a range of clinical research activities, prioritise tasks and meet deadlinesFlexible and open to change and excellent problem-solving abilityNurse AHPRA RegistrationExperience working as a coordinator as blinded/unblinded on commercially sponsored clinical trialsKnowledge and understanding of, GCP, regulatory, ethics, privacy and other applicable guidelinesSample preparation and shipping experienceBe careful - Don't provide your bank or credit card details when applying for jobs.
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