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

In this role, you will:

• Contribute to moderately complex projects, managing time effectively and developing work plans within a team.
• Oversee and conduct real-time study activities and data collection, including those involving mobile medical units.
• Develop protocols based on synopses from the Network Information Server Lead in consultation with the PMS Safety Officer.
• Support medical functions in study management, representing the NHCRU clinic as a Subject Matter Expert for special projects.
• Lead comprehensive reviews, providing expert clinical input on draft study protocols and Informed Consent documents.
• Offer study-specific protocol expertise and input on project planning, timelines, execution, and implementation, including acquiring specialty equipment.
• Ensure clinical oversight, subject safety, and regulatory compliance during shift operations, including weekends and off-shift hours, and provide technical expertise in managing the biometric Subject Verification System.

Here Is What You Need (Minimum Requirements)

• BA/BS with 2+ years of experience or MBA/MS with any years of experience
• Proficiency in public speaking and delivering scientific, medical, and nursing educational presentations
• Proven audit experience, including preparation, development, follow-up, and remediation plans
• Expertise in using the Subject Verification System and various clinical skills
• A solid understanding of the clinical research process
• Good organizational skills and the ability to prioritize tasks
• Fluency in English language

Bonus Points If You Have (Preferred Requirements)

• Master's degree
• Relevant pharmaceutical industry experience
• Work experience in clinical research trials in roles like clinical research nurse, data collector, clinical research technician, study coordinator, or Data Manager
• Experience with Electronic Data Capturing Management System platform
• Strong analytical and problem-solving skills
• Ability to work independently and as part of a team
• Attention to detail and accuracy

  
Work Location Assignment: Hybrid

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

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