11 Nov, 2021

(Senior) Clinical Research Associate - no travel

  • Admin
  • Remote (Melbourne VIC, Australia)
Full time Research Science

Job Description

CRA II/SCRA | no travel | Melbourne office-based with flexibility to WFH or remote elsewhere | Leading NFP

Your new company
This organisation is a leading charitable research organisation that specialises in establishing investigator-initiated clinical trials for their members. You will work on clinical trials initiated by researchers to improve the quality of life and treatment of cancer patients. This incredible charity is offering an exciting opportunity to give back to the community and to contribute fighting a disease that directly or indirectly touches all our lives.
As a permanent, full- or part-time Clinical Research Associate you will be joining a small, collaborative team in Melbourne. With an office located in central Melbourne and close access to public transport, this organisation can offer you the best of both worlds: you will have the flexibility to work from home 2-3 days/ week. We can also consider remote candidates in NSW, SA, TAS, ACT or QLD.

Your new role
In your new role as CRA II or Senior CRA, your responsibilities will include:
  • Primary liaison with investigative sites
  • Develop and maintain study tools (manuals, TMF, etc.)
  • Maintain IP supply
  • Study related documentation
  • Maintain GCP standards on all clinical trials
  • Maintain up-to-date data management of allocated trials including CRF design, data management plan (DMP), data entry, queries and cleaning, data reconciliation, quality control of database
  • Coordinate, prepare and review national (ANZ) Ethical or Regulatory submission activities
  • Conduct all kind of study visits remotely (pre-selection, SIV, ongoing monitoring to close- out)
  • Preparation of reports for periodic review
  • Work closely with the Clinical Project Manager to update on trial progress and escalate issues

What you'll need to succeed
  • A minimum level Bachelor's Degree in Life Science or a related discipline
  • Ideally you will have at least 1-2 years of monitoring experience as a CRA
  • Exceptional communication and time management skills meeting all deadlines
  • Strong understanding of the clinical trials process, ICH Guidelines/SAE reporting, and regulatory requirements
  • Full working rights in Australia
  • Strong desire to work collaboratively in a varied role

What you'll get in return
  • Rewarding role in improving quality of life for cancer patients
  • Not-for-profit salary packaging
  • Highly experienced executive team
  • Work-life-balance
  • Flexible working arrangement
  • Excellent training and development
  • Continuous support and investment into professional training and development
  • Close-knit environment
  • Broaden your expertise and work in a generalist role
  • Run trials from a sponsor's perspective
  • No travel required
  • Competitive salary

What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV to Krisztina Auth krisztina.auth@hays.com.au, or call me now on +61 3 9095 2231.
If this job isn't quite right for you but you are a clinical research professional looking for a new position, please contact us for a confidential discussion on your career.

Remote Status

100% Remote | Work From Home

Apply Now