Clinical Trials Study Coordinator

About the role

Study Coordinator to support the conduct of clinical trials in dementia, including Alzheimer's disease. This is a part-time role, initially requiring Tuesdays and/or Thursdays (9am-4pm) with opportunity to increase hours in the future.

Key responsibilities

• Coordinating and supporting clinical trial activities in accordance with study protocols, ICH-GCP and relevant regulations
• Screening and coordinating study participants
• Liaising with study partners regarding participant visits, assessments and follow-up
• Maintaining accurate documentation and records
• Working collaboratively with investigators, participants, sponsors and other members of the research team
• Supporting study data collection and entry

About you

• Previous experience in clinical trials or research is highly desirable, but not essential
• Experience working with older adults or people living with dementia is advantageous
• Excellent organisational and communication skills
• Strong attention to detail and ability to work independently
• Commitment to providing compassionate, participant-centred care

Benefits

• Flexible hours
• A supportive and collaborative clinical research environment
• Potential for ongoing work as new studies commence