Sr. Director, Global Clinical Research – ITP

About This Opportunity

We are representing a confidential global medical technology organization in their search for a Senior Director, Global Clinical Research focused on infusion therapies and pharmaceutical technologies. This is a senior scientific leadership role responsible for designing and overseeing evidence-generation strategies across a portfolio that includes pharmaceuticals, nutrition therapies, infusion systems, and medication delivery solutions.

Our talent team is seeking a scientifically rigorous leader who can transform medical priorities into executable research programs that generate meaningful clinical, economic, and operational evidence supporting innovation, regulatory submissions, and value-based healthcare initiatives.

Responsibilities

• Partner with Medical Affairs to convert medical evidence priorities into integrated clinical research strategies that address unmet clinical and healthcare system needs
• Design evidence-generation programs using appropriate study methodologies including epidemiology, biostatistics, implementation science, and health-services research
• Develop fit-for-purpose study designs that generate evidence relevant to clinicians, regulators, payers, and healthcare systems
• Serve as the organization's leading expert in clinical research methodology and scientific study design
• Provide scientific oversight for protocols, statistical analysis plans, clinical study reports, and evidence interpretation
• Lead the Clinical Operations team to optimize study feasibility, execution quality, enrollment strategies, and delivery timelines
• Balance scientific rigor with operational feasibility and resource requirements across ongoing studies
• Generate evidence across multiple domains including clinical outcomes, safety, workflow efficiency, human factors, real-world evidence, and health economic outcomes
• Build trusted partnerships across Medical Affairs, Clinical Operations, Regulatory Affairs, R&D, HEOR, Commercial, and Quality functions
• Participate in governance and risk mitigation activities for ongoing studies

What We're Looking For

• Advanced scientific or clinical degree (MD, PharmD, PhD, DNP, or equivalent)
• Minimum 10 years of experience in clinical research, clinical development, medical affairs, or evidence generation
• Proven track record leading development and execution of clinical studies and evidence-generation programs
• Experience working within regulated healthcare environments with strong understanding of GCP and global regulatory expectations
• Expertise generating evidence across pharmaceuticals, medical devices, and healthcare technologies
• Deep understanding of clinical research methodology applied to complex scientific and business questions
• Demonstrated ability to align diverse stakeholders around a common research vision
• Experience building trusted cross-functional partnerships across medical, clinical, regulatory, and commercial teams
• Entrepreneurial mindset with comfort building new capabilities and processes
• Ability to operate effectively in ambiguity and rapidly changing business environments
• Bias toward action and execution while maintaining scientific rigor
• Strong business acumen and impeccable integrity
• Willingness to travel approximately 25% of the time

How We Work With You

Candidates apply directly through Get A Job.ai. Our recruiting team will conduct an initial screening to understand your background and qualifications. If there is a strong mutual fit, we will submit your profile to our client for consideration. Please do not contact the client organization directly—all communication should go through our team to ensure a coordinated and professional process.

Pay

Compensation details will be discussed during the screening process with our recruiting team.

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