AddressClinical Trial Ethics Officer / Start-up Specialist
Immediate Start - Nedlands, Western Australia
Due to continued growth and expansion, we have an exciting opportunity for an experienced Ethics Officer / Start-up Specialist to join a dynamic and growing team.
- Seeking 1.0 FTE Expressions of Interest - part time may be considered for the right applicant
- Onsite and Off site flexibility (must be based in WA)
One Clinical Research (OCR)
OCR is a leader in conducting cancer clinical trials, specialising in pharmaceutical industry-sponsored clinical trials for patients with haematological (blood) or solid-organ cancers.
The successful candidate will primarily be responsible for overseeing essential document collection, preparation and submission of HREC and RGO applications, vendor liaison, eSource creation, regulatory compliance and ensuring efficient and robust governance and start-up timelines of our growing trial portfolio. With an eye for detail and an understanding of GCP they will provide valuable support to the team to ensure adherence to best practice in research processes.
This position will join a close-knit team passionate about optimising patient outcomes in an innovative and progressive clinical trial setting, engaging with various stakeholders to ensure high-quality and efficiently conducted clinical trials, helping to advance access to better treatments for those with cancer.
Essential Criteria:
- Three to five years of highly proficient clinical trial coordinator and/or start-up/ethics coordinator experience
- Demonstrated planning and workload management skills and the ability to independently initiate the tracking, troubleshooting and reporting of trial progress, from Site Selection to Close out
- Demonstrated experience with MS Word, Outlook, Excel, PowerPoint and Access
- High attention to detail with excellent oral and written communication skills
- Personal confidence to liaise with a variety of health and research professionals
- Tertiary qualification in a health or science field
- Demonstrated understanding of ICH-Good Clinical Practice, regulatory, ethical, privacy and other relevant guidelines and legislation relating to clinical trial conduct
Desirable Criteria (at least one of the following):
- Understanding of medical terminology (ideally oncology or haematology context)
- Experience in mentoring junior team members
OCR offers competitive salary options commensurate with experience and responsibility, along with good work-life balance with options for remote working and flexibility.
To apply: Submit a cover letter (that details your working hours/FTE preference) and current CV via Seek.
You must demonstrate the right to work in Australia to be successful in obtaining this position. Please note that only candidates successful in gaining an interview will be notified.
CLOSING DATE: Interviews will be conducted as applications come in so apply early!
For enquiries please contact management at **********@oneclinicalresearch.com.au
