Study Coordinator
Full Time Salary Range $65,000-$80,000 (dependent on experience)
About Us:
At Breast Cancer Research Centre WA (BCRC-WA), we are at the forefront of breast cancer research. Founded by Professor Arlene Chan in 2000, our centre is globally recognised for groundbreaking work that has transformed the treatment of metastatic breast cancer. Located in newly refurbished offices at Hollywood Private Hospital, we're passionate about making a difference in the lives of those affected by breast cancer and are looking for someone whose passion aligns with our purpose.
Position Overview:
As a Study Coordinator, each day brings a mix of administrative tasks, participant interactions, and scientific rigor. It's a rewarding role that contributes directly to groundbreaking breast cancer research.
As a Study Coordinator, you'll play a pivotal role in our mission. You'll collaborate with our Breast Clinical Trials Unit (BCTU) to conduct cutting-edge trials, adhering to regulatory guidelines.
Day-day tasks may include
* Completion of electronic case report forms
* Maintenance and filing of source data and study trackers as required
* Undertaking general administrative duties including booking and confirming participant appointments and patient follow-up visits
* Ensuring investigations and procedures are undertaken as per the protocol
* Assistance with clerical duties relating to each individual clinical trial including filing and site file organisation
* Prepare, attend and monitor visits and study audits
* Preparation and shipping of biological samples
* Assisting with study start up, reviewing protocols, preparing study specific schedules and other documents
* Tasks may vary depending on experience, and training will be provided for those new to clinical trials.
Why join us?:
Purposeful role: Contribute to groundbreaking research where you will be impacting lives.
Full-Time flexible hours: Monday to Friday, 9 am to 5 pm (with flexible start and finish times to suit the team).
Salary Packaging: Up to $15,899 per year plus an entertainment card.
Onsite Parking: Secure undercover parking.
Training: On-the-job training in a supportive environment.
Modern Offices: Work from our newly renovated facilities.
Central Location: Conveniently located in Nedlands near public transport.
Flexible leave Arrangements: Including Time off in Lieu (TOIL).
Qualifications:
Experience: Minimum of 12 months as a Study Coordinator, Clinical Research Associate (CRA), Research Assistant, Healthcare Administrator, Clinical Trial Coordinator, Laboratory Technician.
We welcome applications from motivated individuals looking to start their career in clinical trials.
Skills
* Strong communication skills
* Team Player
* Keen problem solver with an analytical mindset
* Good knowledge and understanding of ICH GCP
* Excellent attention to detail and accurate data entry skills
* Tech-Savvy with proficiency in email, Excel, and Word
Requirements
Legal Status: Australian Permanent Residency or Citizenship.
Oncology Background: Desirable but not mandatory.
If you think you have what it takes and are feeling passionate about our purpose, please apply now