The company is a fast-growing organisation, on a mission to improve world health by expertly managing clinical trials that accelerate medical research.
With state-of-the-art equipment and facilities, the organisation is committed to becoming one of the best early-phase clinical trial service providers in the country.
They are now seeking an Associate Clinical Project Manager/Clinical Project Manager (depending on experience) to join their team.
The aim of the position is to manage the end-to-end delivery of a portfolio of early-phase clinical studies while mentoring a study team that provides operational and administrative support.
You will have to ensure that all studies are being conducted in accordance with the right standards, SOPs, guidelines and regulations - i.e. in line with sponsors' expectations.
This role will suit someone who is driven and who can thrive in a fast-paced environment. You will need to demonstrate a solid entrepreneurial spirit in order to help grow an organisation that is still in its infancy stages.
Responsibilities
* Manage several concurrent trials, ensuring compliance with protocols, reporting requirements and ethical guidelines
* Be a leader and mentor a passionate and dynamic team of clinical trial coordinators, research and data entry assistants
* Oversee the scheduling, recruitment and financial management of clinical trials
* Maintenance of Project Management software/tools to ensure effective milestone tracking and project oversight
* Ensure risk management strategies are implemented
* Ensure continuous stakeholder management
* Exceed sponsor/CRO expectations by ensuring accurate and timely source documentation and data entry, and the maintenance of essential documents that validate integrity in the conduct of the clinical trial.
* Liaise with Principal Investigators, multidisciplinary team members and trial Monitors
Skills and experience
* Tertiary Qualifications in Sciences and/or other related field
* Extensive Clinical Research Project Coordination/Management experience
* Practical working knowledge of clinical trials regulations and guidelines
* Phase I/FIH experience – preferred but not essential
* High attention to detail with the ability to be proactive and take initiative
* Must be a citizen/PR of Australia/New Zealand
* Competitive salary package
* A collaborative, purpose-driven culture that lives by values like Trust, Fulfillment, and Innovation
For more details, please contact Chris on chris.danchald@tardis-group.com
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