Support the marketing and recruitment of participants into clinical trials, improving access and inclusion for members of our local communities.
Assist in the coordination of clinical trials, including participant scheduling, screening and data collection.
Ensure that trials are conducted in compliance with ethical standards and regulatory guidelines.
Provide administrative support for trial-related activities such as medical administration duties, clinic management and phone duties.
Work closely with investigator staff to monitor participant wellbeing and ensure patient safety and wellbeing.
Support the collection and management of trial data, ensuring accuracy and confidentiality.
Communicate with research teams, sponsors, and participants to facilitate smooth trial operations.
Requirements
Strong organisational skills and attention to detail, with the ability to manage multiple tasks and meet deadlines.
Excellent communication and interpersonal skills, with the ability to work collaboratively with clinical investigators, members of the multidisciplinary team and participants.
Understanding of clinical trial regulations, ethics, and protocols is beneficial.
Computer literacy, including proficiency with data entry and management software.
A proactive and flexible attitude, with a commitment to maintaining the highest standards of participant safety and data integrity.
Previous experience in clinical trials, healthcare, or research environments is highly desirable.
Benefits
Collaborative, passionate and welcoming culture.
Modern teaching & research facilities.
Professional development and career pathway opportunities.
EAP & discounted private health.
Notes
To maintain currency of this register, applications will be removed on 31 December, 2024. Please re-apply after this date if you wish to be considered for suitable opportunities.