Clinical Research Coordinator Nuclear Medicine

Clinical Research Coordinator Nuclear Medicine

The Research Trial Coordinator/Data Manager Nuclear Medicine is involved in clinical trials and research within the department of Nuclear Medicine.

Employment Type: Temporary Full Time until 15 October 2029 (with possibility of ongoing employment)
Position Classification: Health Manager Level 1
Remuneration: $1,563.50 - $2,080.01 per week
Hours Per Week: 38
Requisition ID: REQ526307

Who we are: We are a health service that touches thousands of lives across the Northern Sydney Local Health District, together as a team of like-minded people. We are passionate, driven and have the skills and knowledge to care for our patients whilst creating the best services possible. Our teams have meaningful, interesting and rewarding work everyday. We challenge and nurture each other, sharing our knowledge and experience so that we can deliver better care for everyone There’s a real sense of belonging here because we value and respect our patients, employees, and teams’ voices. You’ll feel a real privilege being a trusted caregiver in our patients, their families, their carers, and our communities’ lives.

NSLHD is proud of our diverse and inclusive workplaces, a place where health care professionals can thrive and feel they belong. We are committed to ensure that all our people feel respected and participate safely within a work environment without aggression, sexual harassment, discrimination and racism.  

Where you'll be working
Royal North Shore Hospital, Nuclear Medicine

What you'll be doing

The Research Trial Co-ordinator / Data Manager works closely with researchers and clinical staff within the Department of Nuclear Medicine to co-ordinate and manage clinical trial activities. 

People of Aboriginal and/or Torres Strait Islander background encouraged to apply.

Candidates will need to meet the following criteria:

1. Tertiary qualification at a graduate level in a health or science discipline or equivalent research/clinical trial experience including an understanding of the ethics submission process in a hospital environment
2. Outline your experience with clinical trials in a hospital setting.
3. Experience with software relevant to clinical research
4. Experience in a Team related to research.