Study Start Up Specialist- Clinical Trials

15 hours ago

Camperdown, Australia Chris O’Brien Lifehouse Full time

Chris O’Brien Lifehouse is an internationally recognised independent, not-for-profit cancer hospital leading the way in delivering patient-centred cancer care. We seek passionate, caring, and dedicated staff who align with our Founder’s vision of creating a collaborative environment in which, respect, discovery, empowerment, and nurture, thrive in the interests of our patients._

**The Role**

As a member of the Study Start-Up team, this position reports to the Business Manager of Clinical Trials, to ensure the timely management of clinical trial contracts are negotiated with sponsors to ensure all costs are in-line with the relevant clinical trial protocol. This position is part of a small team that works closely with a multi-functional team consisting of doctors, pharmacists, clinical study coordinators, data managers, internal start-up specialists, study sponsor teams, and clinical research associates to assist in conducting early phase clinical research trials.

**Selection Criteria**
- Ability to work autonomously and as a team member that is inclusive, approachable and supportive
- Previous budget negotiation experience
- Good negotiating and communications skills with the ability to challenge, if applicable
- Demonstrated high level of interpersonal skills, including verbal and written communication
- Ability to manage multiple projects
- Ability to establish and maintain effective working relationships with colleagues, managers, and clients
- Problem solving with a strong focus on accuracy
- Excellent planning and organisational skills to prioritise tasks and meet deadlines
- Attention to detail and proactive nature
- Knowledge of Clinical trials and or Good Clinical Practice (GCP) - desirable
- Evidence of immunisations to comply with the NSW Health Occupational Assessment, Screening & Vaccination against Specified Infectious Diseases Policy for a Category B position

**Key responsibilities**
- Review and negotiate itemised budgets that incorporate all the costs for a trial in accordance with the relevant clinical trial protocol with Sponsors, including resolution of concerns to her mutual satisfaction of all parties
- Amend budgets and contracts due to protocol amendments by the sponsor
- Ensure regular communication & escalation to expedite issue resolution & execution of contracts

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