Use Your Power for Purpose

Our mission is straightforward: empower healthcare decisions regarding the safe and appropriate use of medicines for patients. Whether you are developing the framework to ensure our evidence is scientifically robust, providing unbiased and medically essential expertise, or exploring ways to bridge data gaps, your role is vital. By ensuring our evidence is sound and offering necessary medical insights, we strive to improve patient care and treatment efficacy.

What You Will Achieve

• Develop and lead complex projects, managing plans to achieve objectives and ensuring alignment with business unit goals.
• Manage clinical studies, utilizing project management skills to plan, direct, and communicate timelines, ensuring studies are within time, budget, and scope.
• Develop and manage plans to achieve objectives, interpreting business challenges, and recommending best practices for improvements.
• Anticipate and troubleshoot roadblocks in complex project environments, influencing teams to achieve division targets.
• Oversee Study Startup, Study Monitoring, protocol recruitment plans, and resolve escalated issues in collaboration with the Study Manager.
• Manage Operational Study Management, Clinical Trial Budget, and drug supply, working with CROs and data management teams to ensure timely data flow and delivery, and participating in global initiatives to enhance operational efficiencies.

Here Is What You Need (Minimum Requirements)

• BA/BS with 6+ years of experience or MBA/MS with 5+ years of experience or PhD/JD with 1+ year of experience or MD/DVM with any years of relevant experience
• Proven project management and leadership experience, including oversight of CROs
• Working knowledge of Good Clinical Practices, monitoring, and clinical and regulatory operations
• Ability to evaluate, interpret, and present complex issues and data to support risk
• Excellent communication skills, both written and verbal, with fluency in English
• Effective decision-making, analytical, and solution-oriented skills
• Proficiency in the Microsoft Office Suite

Bonus Points If You Have (Preferred Requirements)

• A Master's degree with broad-based experience in clinical research
• Demonstrated ability to lead cross-functional teams
• Excellent organizational and time management skills
• Ability to influence and collaborate with diverse stakeholders
• Strong interpersonal skills and the ability to work effectively in a team environment

  
Work Location Assignment: Remote

At Pfizer we care about our colleagues’ wellbeing and offer a range of great benefits for them, including:

• Paid parental leave

• Access to Health & Wellness apps

• Career Growth Experiences program

• Recognition & rewards program

• Paid volunteer days

• Life Insurance Benefits

• Pfizer Learning Academy access to top content providers

• Access to flu vaccines & skin checks

• Options to purchase additional leave

• Salary packaging & novated lease options

*Benefits listed may vary depending on your position and location and may be subject to change.

Pfizer Australia and New Zealand’s diverse workforce represents the patients we serve and the communities in which we operate. With a focus on Diversity, Equity & Inclusion (DE&I), Pfizer ANZ ensures our people are heard and cared for. We offer engagement opportunities in both Colleagues Resource Groups (CRGs) and workstreams across: Culture and Tradition, Reconciliation @ Pfizer (RAP), Gender Equity (GEN), Disability and through the Out Pfizer Employee Network (OPEN) for our LGBT + colleagues and allies.

If you require reasonable adjustment during your application, please reach out to the Talent Acquisition Manager.

Medical

#LI-Remote #LI-PFE