Tammy Ice

About Tammy Ice

With more than two decades of experience in patient engagement, I bring unique subject matter expertise not only in patient recruitment and retention, but also in the complex clinical research and pharmaceutical management spaces. I advocate for patient-focused programs that make a space at the table for patients and their caregivers to contribute their valuable experiences, insights, and priorities—all with the goal of improving the way we do R&D. When the trials are complete and the drug is ready, I bridge the gap between clinical learnings and marketing strategy to help pharma companies to package and position newly-approved medications to compete in the marketplace. The bottom-line impact of my work: reduced enrollment times, accelerated time to delivery, lower operating costs, and—most importantly—better patient outcomes.My Strengths: TEAM LEADERSHIP: As a leader, my proudest achievements are not actually my own. By focusing on my team’s accomplishments before my own and coaching each person individually, I empower and celebrate the success of the next generation of executive professionals. BUILDING BRIDGES: My global understanding of drug development dependencies and vast network of professional relationships in the CRO ecosystem allows me to understand executive decision-makers’ priorities and add significant value to every conversation. CHANGE AND INNOVATION: Like the therapeutics we work to green-light, our systems and tools are also evolving at an incredible pace. I have a strong record of implementing new technologies, engagement platforms, and analytics techniques that add value on multiple levels.

Experience

1. Vice President, Patient Experience

   AMR Clinical

   Jan 2025 — Present · US

   Establish a comprehensive patient experience strategy accelerating clinical trial delivery•Collaborate cross-functionally with clinical operations to embed patient-centric practices into study design and execution, improving trial outcomes and participant retention.•Design and implement systems for collecting and analyzing patient feedback, driving continuous improvement through data-informed decision-making.•Develop educational resources and communication strategies to address patient concerns, fostering trust and transparency throughout the clinical trial journey.•Utilize data analytics to monitor patient experience metrics, identify trends, and implement targeted improvements aligned with trial objectives.•Ensured compliance with ethical standards and regulatory requirements, including GCP, while safeguarding patient rights and confidentiality.•Present strategic reports and insights to executive leadership, translating patient experience data into actionable recommendations.

Education

• Lenoir-Rhyne University

  Bachelor of Arts - BA, Communication

Skills

• Project Management
• Good Clinical Practice (Gcp)
• CRO Management
• Regulatory Submissions
• Oncology
• Protocol
• Pharmaceutical Industry
• Sop
• Clinical Monitoring
• Clinical Trial Management System (Ctms)
• Clinical Research
• Gcp
• Therapeutic Areas
• Ctms
• Clinical Trial Management
• Ich-Gcp
• Patient Recruitment
• Clinical Trials
• Pharmaceuticals
• Biotechnology
• CRO
• Regulatory Affairs
• Media Planning
• Advertising
• Infectious Diseases
• Clinical Development