Pfizer Australia Pty Ltd is hiring a Site Care Partner II

Pfizer Australia Pty Ltd is looking for a Site Care Partner II to be the key point of contact for investigative sites, ensuring quality and patient safety from study start-up through to close-out. You will play a critical role in optimizing site selection, building strong relationships, and providing operational support to drive successful study delivery in a patient-centric environment guided by courage, joy, equity, and excellence.

What You'll Do

• Account for site start-up and activation, including qualifying and activating assigned sites and deploying site strategies.
• Optimize country and site selection by reviewing potential site lists and providing country-level input to feasibility and protocol design.
• Conduct site-level start-up activities, including Pre-Trial Assessment (PTA), finalizing Informed Consent Documents (ICD), and managing the Site Initiation Visit (SIV).
• Ensure all site initiation activities and training are completed per the activation checklist to achieve site readiness.
• Partner with CRA/site monitors to ensure site monitoring readiness for the first subject first visit.
• Build and maintain effective relationships with Site Organizations and Strategic Partners.
• Be accountable for effective site recruitment planning and delivery, consistent with global and local targets.
• Provide study support on escalated site issues, coordinating communications and resolution efforts.
• Manage the strategy for investigational product and ancillary supplies throughout the study lifecycle.
• Account for study conduct and close-out, reviewing Site Reports and updating Site Management Organization Assessments.
• Inform and educate investigator sites on relevant Pfizer pipeline opportunities.
• Support the development and delivery of decentralized capabilities at sites, such as home health and ePRO.
• Demonstrate leadership within the local clinical development environment and act as a Subject Matter Expert on systems and processes.
• Proactively provide local intelligence for country strategy and site recommendations.

What We're Looking For

• Bachelor’s degree, RN in a related field, or equivalent combination of education, training, and experience.
• 7+ years of relevant experience with demonstrated site management expertise and prior experience as a CRA/site monitor.
• Proven experience in start-up activities through to site activation, as well as in study conduct and close-out activities.
• Demonstrated knowledge of quality and regulatory requirements in applicable countries, including Good Clinical Practice/ICH Guidelines.
• Excellent communication, presentation, interpersonal, and networking skills.
• Ability to manage required travel, build cross-functional relationships, and communicate effectively with internal and external stakeholders.
• Strong computer skills with the ability to adapt to new technologies and processes.
• Knowledge of country-specific GCP requirements that may differ from Pfizer procedures.
• Fluency in Greek and English.

Team & Environment

You will coordinate with other roles and functions that interface with study sites, such as CRA/Site Monitors, Investigator Contracts Leads, Site Activation Partners, and Clinicians, reporting to a Study Operations Manager or Global Study Manager.

Work Mode

This is a remote position.

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