Krista Zielinski

About Krista Zielinski

With over 15 years in the life sciences industry, I’m passionate about helping organizations achieve operational excellence through innovative, flexible solutions. I recently joined IQVIA as Associate Director, Data Sciences, Safety, and Regulatory FSP Sales, where I focus on delivering Functional Service Provider (FSP) models that empower clients to meet strategic goals.What we do: IQVIA’s FSP services provide specialized, scalable resources across Safety, Regulatory, and Data Sciences—including pharmacovigilance, global regulatory strategy, and advanced analytics to support clinical development and real-world evidence.Why it matters: In a rapidly evolving landscape, FSP solutions offer agility, efficiency, and quality—helping organizations manage complexity, reduce risk, and accelerate timelines.How we deliver: Through flexible partnerships, IQVIA combines deep expertise, global reach, and cutting-edge technology to integrate seamlessly with client teams and drive measurable outcomes.I welcome the opportunity to connect and discuss how IQVIA’s FSP-driven solutions can help your organization achieve greater flexibility, efficiency, and innovation.

Experience

1. Associate Director, Data Sciences, Safety, and Regulatory Fsp Sales

   IQVIA

   Nov 2025 — Present · US

   Associate Director for FSP Sales at IQVIA, specializing in Data Sciences, Safety, and Regulatory. I drive growth by building strategic partnerships, identifying client needs, and delivering tailored FSP solutions across Data Management, Biostatistics, Programming, Medical Writing, Lifecycle Safety, and Regulatory Affairs. Focused on helping life sciences organizations achieve agility, efficiency, and innovation through flexible service models.

Education

• University of Florida

  Bachelor of Arts (B.A.), English Language and Literature/Letters

  2004 — 2006

Skills

• Medical Affairs
• Medical Coding
• Pharmacovigilance
• Pharmaceutical Industry
• Drug Safety
• Data Management
• Ctms
• Quality Assurance
• Medical Information
• Clinical R
• Biotechnology
• Clinical Data Management
• Clinical Trials
• Epidemiology
• Clinical Project Management
• Regulatory Affairs
• Medical Writing
• Medical Directors
• Clinical Operations
• Biostatistics
• Clinical Research Organization
• Clinical Trial Management
• Contract Recruitment
• Medical Devices
• Clinical Research
• Clinical Documentation
• Recruiting
• Pharmaceuticals
• Strategy
• Cra