Clinical Coordinator

Pfizer • New Haven, CT

3d • $79,400 - $132,400 • Onsite

About The Position

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.

Requirements

• BA/BS or MBA/MS with at least 2 years of experience in the Research Industry.
• At least 2 years of experience as a Clinical Research Coordinator or roles closely related as a Clinical Research Coordinator
• At least 2 years of experience in relevant pharmaceutical industry roles
• Proficiency in public speaking and delivering scientific, medical, and clinical educational presentations
• Proven audit experience, including preparation, development, follow-up, and remediation plans
• A solid understanding of the clinical research process
• Good organizational skills and the ability to prioritize tasks
• Fluency in English language
• Attention to detail and accuracy

Nice To Haves

• Master's degree
• Clinical Research Certification
• 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
• Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use

Responsibilities

• Contribute to 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.
• Contribute to protocol development within the NHCRU internal team
• 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, good clinical practice and regulatory compliance during shift operations, including weekends and off-shift hours, and provide technical expertise in managing the biometric Subject Verification System.

Benefits

• 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
• paid vacation, holiday and personal days
• paid caregiver/parental and medical leave
• health benefits to include medical, prescription drug, dental and vision coverage
• Relocation assistance may be available based on business needs and/or eligibility.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree