Job DescriptionA unique chance to join a state of the art centre in Sydney has developed for a Clinical Trials Project Manager to lead a team of PMs and coordinators in their operations. A brief snapshot of the role is below, but please get in touch for more information and a more detailed job spec.
About the role:
Creation of project plans; tracking and communicating projects progress; and adapt project strategies as required.
Ensure appropriate tools and resources are available for tracking of all version-controlled documentation. Evaluating effectiveness of tools on an ongoing basis.
Oversight of risk assessment for each clinical trial; assist in the development and implementation of appropriate risk management plan; and ensure the plan is monitored throughout the life cycle of the project.
Develop strategies for high quality data entry for CRF completion within agreed timelines.
Be accountable for the management and filing of all essential documents in compliance with Good Documentation Practice, GCP, SCR and Sponsor requirements in a timely manner; remain inspection ready at all times.
Ensure that all studies are managed and conducted according to SCR SOPs, and policies, applicable regulations as well as ICH GCP E6R2 and NHMRC guidelines to meet the regulatory requirements for registration.
A leader in Clinical Trials with an Oncology trial background
At least 5 years managing clinical studies
Excellent attention to detail and ability to drive teams
If you feel you're right for the role, please just get in touch!