Clinical Project Manager - Oncology start-up

Job title: Clinical Project Manager - Oncology start-up
Contract Type: Permanent
Location: Sydney, Australia
Salary: $150000 - $155000 per annum, Benefits: Bonus, WFH
Reference: BH-118828
Contact Name: Christopher Parkinson
Phone Number: +61 2 9696 8005
Job Published: 13 days ago

Job Description

Are you a talented Clinical Trial Manager looking for a new role outside of your traditional CROs? Maybe a smaller, dynamic team environment where one day is totally different to the next? Then this role may well pique your interest as it a challenge we don't often see on the market. 

You will be accountable for project management of clinical trials within the newly formed CRO organisation.
  • Project management of assigned activities related to the management of clinical trials
  • Manage the implementation, ongoing evaluation, prioritisation, reporting and timely delivery of all operational aspects of allocated projects
  • Ensure clinical trial projects are properly resourced, managed and executed within budget and in accordance with established timelines and quality standards
  • Work closely and effectively with sponsor study teams. Make recommendations to and seek guidance from the sponsor or the project leader.
  • Maintain effective professional relationships with sponsor, external customers, investigators, vendors and the internal project team
  • Provide clear guidance to the project team on project specific deliverables as defined in contracts and project specific documentation
  • Oversee the preparation of study essential documents: prepares protocol, amendments, CRF, informed consent form, operations and other documentation required for conduct of a clinical trial. The CPM may also prepare required regulatory documents, such as annual reports, updating of the IB, and final study reports for assigned protocols
  • Undergraduate degree in Life Sciences (e.g., Biology, Chemistry, Pharmaceuticals)
  • Strong experience in clinical research in CRO (preferable), Pharmaceutical and/or Biotechnology industry, as a Project Manager
Proven track record of having successfully led complex global clinical trials, with experience across all functional capabilities involved in CRO-directed clinical research (project management, medical & scientific affairs, safety/pharmacovigilance, quality assurance, data management, site-related activities

About You: 
  • Self-motivated leader, high energy and empathy, influence capabilities and interpersonal savvy across all levels of the organisation
  • Ability to think strategically and tactically about CRO development including short- and long-term impact on business and purpose
  • Demonstrated ability to handle and oversee multiple tasks simultaneously and to prioritize in a meaningful way
Please just get in touch to start the next chapter of your career!