Associate Director, Digital Health MedTech Clinical

The Associate Director, Digital Health Studies provides senior leadership for the delivery of digital health clinical research programs, including decentralized and hybrid clinical trials, connected devices, digital therapeutics, AI-enabled healthcare technologies, wearable solutions, and other technology-enabled study models.

This role serves as a sponsor-facing leader responsible for clinical oversight, operational excellence, and cross-functional collaboration across the study lifecycle. The Associate Director will play a key role in growing and scaling IQVIA's Digital Health practice by ensuring high-quality execution, supporting business development efforts, and developing organizational capabilities in this rapidly evolving area. 

• Provide leadership and oversight for digital health clinical studies from study start-up through closeout.
• Ensure studies are executed in compliance with ICH-GCP, regulatory requirements, and company quality standards.
• Serve as the escalation point for clinical, operational, quality, and technology-related issues.
• Drive consistency and best practices across digital health study delivery.

• Serve as a primary point of contact for sponsors and senior stakeholders.
• Lead governance meetings, study reviews, and executive-level communications.
• Build and maintain strong relationships with sponsors, investigators, vendors, and cross-functional teams.

• Support proposals, bid defenses, and client presentations.
• Provide subject-matter expertise across digital health, decentralized clinical trials, connected devices, and emerging healthcare technologies.
• Contribute to the development of scalable delivery models and service offerings.

• Mentor and develop project managers, clinical staff, and study teams.
• Support hiring, onboarding, and professional development initiatives.
• Foster a culture of accountability, collaboration, and continuous improvement. 

• Bachelor's degree in Life Sciences, Healthcare, Public Health, Nursing, Technology, or a related field. Advanced scientific, clinical, public health, or related healthcare discipline strongly preferred.
• 7+ years of clinical research experience, including experience supporting digital health, medical device, or technology-enabled clinical studies.
• Experience leading complex, multi-study clinical research programs.
• Strong understanding of ICH-GCP, clinical trial operations, and regulatory requirements.

• Experience with decentralized and hybrid clinical trial models.
• Experience supporting one or more of the following:
  • Digital Therapeutics (DTx)
  • Connected Medical Devices
  • Software as a Medical Device (SaMD)
  • AI-Enabled Healthcare Solutions
  • Wearable Technologies
  • Remote Patient Monitoring
  • Radiology or Imaging Technologies
• Familiarity with EDC, CTMS, ePRO, and other clinical technology platforms.

• Strong leadership and client management skills.
• Excellent communication and presentation abilities.
• Ability to manage multiple priorities in a fast-paced environment.
• Strong problem-solving and decision-making capabilities.
• Advanced proficiency with Microsoft Office applications

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.