Senior Study Coordinator

Senior Clinical Research Assistant

Breast Cancer Research Centre WA (BCRC-WA), is a world leader and is one of the most highly regarded breast cancer clinical trials unit in Australia, located in newly furbished offices at Hollywood Private Hospital. 

The centre, founded by Professor Arlene Chan, in 2000, is recognised globally for its ground-breaking breast cancer research. To date, at least 13 BCRC-WA trials have improved the way metastatic breast cancer is treated internationally. 

As a purpose driven organisation you will be amongst the best, working in one of the busiest, fast paced and dynamic clinical trials unit In Western Australia.  We are dedicated to nurturing medical breakthroughs and as a Senior Clinical Research Assistant, you can be part of that success and work for an organisation where you can truly make a difference in the lives of those with breast cancer and breast cancer research.

What we are offering the successful candidate: 

• Full time, 12-month fixed term contract 
• Monday to Friday 9-5pm with flexibility if needed. 
• A competitive salary
• up to $15,899 Salary Packaging per year, plus an entertainment card up to $2,650 per year
• Free onsite, secure undercover parking
• On the job training
• New offices to work from
• Central Nedlands location, close to public transport
• Flexible leave arrangements including Time off in Lieu (TOIL)

Your role in our future:

We are looking for a passionate and experienced Senior Clinical Research Assistant to be responsible for the oversight and delivery of multiple clinical trial projects within our unit.

Responsibilities will include:

• Prepare and maintain trial documentation and records.
• Coordinate and oversee the project teams to ensure project milestones and deliverables are met.
• Identify and address any breaches of guidelines and regulations.
• Assist in the preparation of ethics, if needed
• Oversee the preparation and follow-up of monitoring visits and be the site representative for such visits.
• Provide feedback on AEs and SAEs in alignment with relevant guidelines.
• Maintain oversight of project costs ensuring trials are delivered in accordance with budgets.
• Support the clinic team with study activities, as required.
• Provide training and mentoring to junior clinical research assistance

Your experience:

You will be an individual who takes initiative whilst handling competing priorities. The key to your success will be a tertiary qualification in a related field (Science or Business) and a minimum of 2-3 years’ experience in a clinical trial environment.

You will further have:

• Understanding of clinical trial protocols and Good Clinical Practice.
• Proven ability to resolve project-related problems and prioritise workload.
• Strong financial acumen, ability to apply financial principles.
• Project planning, coordination, evaluation, and management skills.
• Excellent verbal and written communication skills.
• A high level of attention to detail with ability to work within guidelines and procedures.
• Excellent organisational skills, flexibility, and ability to work under pressure.
• Computer proficiency.
• Ability to work autonomously and as part of a team.

If this sounds like you, please apply now!