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Clinical Trial Coordinator/Assistant

2 weeks ago

Perth, Western Australia One Clinical Research Full time $80,000 - $120,000 per year

Various Clinical Trial Coordinator/Assistant Roles Available

Immediate Start Available - Nedlands, Western Australia

Exciting opportunities for experienced Clinical Research Professionals to join a dynamic and growing team. Positions available include:

  • Senior CTC/Project Lead
  • CTC (Clinical Trial Coordinator)
  • CTA (Clinical Trial Assistant)

Full time positions preferred (part time EOIs also considered).

One Clinical Research (OCR)

OCR is an emerging leader in clinical trials, specialising in pharmaceutical industry-sponsored clinical trials for patients with haematological (blood) and solid-organ cancers, and chronic diseases.

The successful candidate(s) will primarily be responsible for day-to-day execution of a range of clinical trials, spanning Phase I first-in-human clinical trials through to Phase III randomised trials. The role will focus on planning and execution of participant visits, preparation of source documents, collection of participant data, data entry, liaising with trial monitors, and maintenance of the investigator site files across our growing portfolio of clinical trials.

This position will join a close-knit team passionate about optimising patient outcomes in an innovative and progressive private 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 and chronic illness.

Essential Criteria:

  • Highly proficient clinical research assistant or clinical trial coordinator
  • Demonstrated planning and workload management skills and the ability to work autonomously
  • Demonstrated experience with MS Word, Outlook, Excel, PowerPoint
  • High attention to detail, with excellent oral and written communication skills
  • Personal confidence to liaise with a variety of health and research professionals
  • 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):

  • Tertiary qualification in a health or science field, or equivalent experience
  • Understanding of medical terminology (ideally oncology or haematology context)
  • Experience in electronic source documentation
  • Knowledge/skills in clinical assessments of participants, or willingness to learn (e.g. vitals, ECG, sample processing)

OCR offers competitive salary options commensurate with experience and responsibility, along with good work-life balance with options for remote working (where appropriate) and flexibility.

To apply: Submit a cover letter 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