Platelet Clinical Research Coordinator
Vor 4 Tagen
Employment Type: Temporary Part Time until 28 March 2027 (with possibility of ongoing employment)Position Classification: Health Manager (Level 1)Remuneration: $42.58 - $56.65 per hourHours Per Week: 19Requisition ID: REQ539860 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 workingHaematology, Royal North Shore Hospital What you'll be doing Coordinate haemostasis clinical trials within the Haematology Department at Royal North Shore Hospital.
Ensure research is conducted in accordance with the protocol, policy, legislation, ethical requirements, and guidelines for Good Clinical Practice and the National Statement on Ethical Conduct in Human Research.People of Aboriginal and/or Torres Strait Islander background encouraged to apply.Candidates will need to meet the following criteria: Relevant tertiary qualifications or experience in planning, coordination and conduct of clinical trials or equivalent.
Previous experience with haematology patient population.
Demonstrate haemostasis clinical trial experience, including a working knowledge of ICH GCP and other regulatory and ethical requirements in the conduct of clinical trials in Australia.
Demonstrate organisational and time management skills and the ability to adhere to deadlines without compromising close attention to detail and accuracy.
Demonstrate experience completing ethics/governance applications and progress reports via REGIS.
Demonstrate strong computer skills including word processing, experience with Microsoft Windows based applications and clinical trial databases.
Demonstrate ability to function both autonomously and within a collaborative team environment.
Highly effective communication, negotiation and interpersonal skills essential.
Need more information?
1) Click here for the Position Description 2) Find out more about applying for this positionFor role related queries or questions contact William Stevenson on ****** Applications Close: 6 January 2025
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