Senior Clinical Research Manager

BENEFITS
Hybrid work, 1-2 days per week in office (choose your days, consistent team collaboration days where possible)
35 hour work week, flexible hours agreements & 9-day fortnights
Salary Packaging: $15,900.00 of your base salary tax free & up to $2650.00 meal & entertainment
Family first, people first culture, we put our research into action at work to make sure we maintain mental health and wellbeing at work
Pet friendly workplace
THE ROLE
The Clinical Research Manager will play a leading role in planning, coordinating, and supervising a Clinical Research project involving the development and trial of a blended care intervention for adolescents with depression. They will bring excellent leadership and time management skills, the ability to establish and maintain effective working relationships with a range of senior and external stakeholders including clinicians, and a creative and ‘can do’ attitude to problem solving.
The successful candidate will oversee the running of a major Clinical Research project and will be accountable for ensuring that responsibilities are performed according to quality standards, budgets and timelines and that project milestones are delivered on time and to a high standard. The role will work closely with the Chief Investigators for this project and will provide project management and coordination for the blended care project.
The role reports to one of the Chief Investigators (Associate Professor) and will have at least 1 direct report.
DUTIES & RESPONSIBILITIES
Project Management:
Lead and manage the development of the project and implementation plan to ensure successful delivery of the project within agreed timeframes, resources and budget.
Planning project management, including setting deadlines, prioritising tasks, and assigning team members to various deliverables.
Provide project reports, including budget and risk outlines, to the budget holders and funder.
Write clear and concise specifications, reports, project management plans, business cases, project schedules budgets and briefing notes and communicate effectively with a variety of audiences.
Research:
Provision of practical and efficient research support to the research team.
Develop the ethics applications and amendments for submission, maintaining the master study file.
Proactively assist with research reports, peer-reviewed publications, presentations, ethics applications and progress reports.
Support in the conceptualisation, design, and successful conduct of research projects related to this project, including a clinical trial.
Provision of administrative and clerical duties, including attendance at research meetings, preparing meeting agendas, preparing and distributing minutes, as required.
Monitor research protocols, provide problem solving and resolution to any evolving problems related to design, implementation and analysis.
Coordinate reporting activities to Data Safety Monitoring Boards and other relevant groups.
Stakeholder Management:
Liaise with clinicians (psychologists, Apply Now