17 Oct
Pfizer
Haymarket
Pfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary expertise or investigating how to close gaps in data, our mission is simple. Empower healthcare decisions regarding the safe and appropriate use of medicines for patients. What You Will Achieve You will be part of Pfizer's medical team and manage the clinical studies. Your project management skills will be leveraged for planning, directing, creating and communicating timelines.
You will ensure that the clinical studies are within time, budget and scope. As a Site Care Partner, your advanced knowledge of the principles and concepts in the discipline and comprehensive knowledge of other disciplines will enable you to lead complex projects across the division. Your ability to develop and manage plans will facilitate in achieving objectives, interpreting internal and external business challenges and recommending best practices for improvements. While managing complex project environments, you will be able to anticipate and troubleshoot roadblocks and influence teams to achieve targets for the division. It is your problem solving ability and patience that will make Pfizer ready to achieve new milestones and help patients across the globe. How You Will Achieve It Develop ideas, lead/co-lead complex projects across business units and develop plans to achieve objectives. Approve the Study Startup, Study Monitoring and protocol recruitment plans.
Resolve escalated issues identified by the site activation subteam in partnership with the Study Manager. Work proactively with
Clinical Research Organizations (CRO ) and data management functions to ensure alignment on data flow and timely delivery. Manage Operational Study Management for one or more studies of limited complexity or a unique part of a larger study. Forecast and manage the Clinical Trial Budget for the program. Provide country and regional level input to country outreach surveys. Create awareness by working as a cross functional Team Leader to deliver site intelligence initiatives with a variety of stakeholders, both internal and external. Approve and oversee drug supply management, manage flow of drug supply to the sites. Participate in global initiatives to improve operational efficiencies.
Evaluate study progress reports and results for overall compliance and recommends corrective action or study termination for non-performance. Maintain regular communications with investigator sites to gather status updates, informal and formal performance metrics, and study-level feedback. Qualifications Must-Have Bachelor's Degree 7+ years' experience Applicable pharmaceutical industry experience Working knowledge of Good Clinical Practices, monitoring, clinical and regulatory operations Demonstrated project management / leadership experience Experience with CRO oversight Ability to evaluate, interpret and present complex issues and data to support risk Excellent communication skills,
both written and verbal; must be fluent in English Effective decision maker, analytical and solution-oriented Proficiency in Microsoft Office Suite Nice-to-Have Broad based experience in clinical research Strong knowledge of and interest in
Oncology Therapeutic Space
, subject matter expertise and international experience Why Patients Need You Pfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary expertise or investigating how to close gaps in data, our mission is simple.
Empower healthcare decisions regarding the safe and appropriate use of medicines for patients. What You Will Achieve You will be part of Pfizer's medical team and manage the clinical studies. Your project management skills will be leveraged for planning, directing, creating and communicating timelines. You will ensure that the clinical studies are within time, budget and scope. As a Site Care Partner, your advanced knowledge of the principles and concepts in the discipline and comprehensive knowledge of other disciplines will enable you to lead complex projects across the division. Your ability to develop and manage plans will facilitate in achieving objectives, interpreting internal and external business challenges and recommending best practices for improvements. While managing complex project environments,
you will be able to anticipate and troubleshoot roadblocks and influence teams to achieve targets for the division. It is your problem solving ability and patience that will make Pfizer ready to achieve new milestones and help patients across the globe. How You Will Achieve It Develop ideas, lead/co-lead complex projects across business units and develop plans to achieve objectives. Approve the Study Startup, Study Monitoring and protocol recruitment plans. Resolve escalated issues identified by the site activation subteam in partnership with the Study Manager. Work proactively with
Clinical Research Organizations (CRO ) and data management functions to ensure alignment on data flow and timely delivery.
Manage Operational Study Management for one or more studies of limited complexity or a unique part of a larger study. Forecast and manage the Clinical Trial Budget for the program. Provide country and regional level input to country outreach surveys. Create awareness by working as a cross functional Team Leader to deliver site intelligence initiatives with a variety of stakeholders, both internal and external. Approve and oversee drug supply management, manage flow of drug supply to the sites. Participate in global initiatives to improve operational efficiencies. Evaluate study progress reports and results for overall compliance and recommends corrective action or study termination for non-performance. Maintain regular communications with investigator sites to gather status updates,
informal and formal performance metrics, and study-level feedback. Qualifications Must-Have Bachelor's Degree 7+ years' experience Applicable pharmaceutical industry experience Working knowledge of Good Clinical Practices, monitoring, clinical and regulatory operations Demonstrated project management / leadership experience Experience with CRO oversight Ability to evaluate, interpret and present complex issues and data to support risk Excellent communication skills, both written and verbal; must be fluent in English Effective decision maker, analytical and solution-oriented Proficiency in Microsoft Office Suite Nice-to-Have Master's degree. Broad based experience in clinical research Strong knowledge of and interest in
Oncology Therapeutic Space
, subject matter expertise and international experience
Work Location
Assignment: Flexible 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-PFE
About Us
Pfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare, and potential to transform millions of lives. We’re looking for new talent to join our global community, to unearth new innovative therapies that make the world a healthier place.
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