
10,000+ employees
Founded 1849
💰 Post-IPO Debt on 2023-05
We’re celebrating 175 years of daring scientific innovation—and we’re not done yet. Every day, we’re channeling our passion and resources into delivering innovative therapies that change the face of healthcare. Let’s outdo yesterday.
🔥 0 minutes ago
🐊 Florida – Remote
💵 $230.9k - $384.8k / year
⏰ Full Time
🔴 Lead
👨⚕️ Medical Director
🦅 H1B Visa Sponsor
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10,000+ employees
Founded 1849
💰 Post-IPO Debt on 2023-05
We’re celebrating 175 years of daring scientific innovation—and we’re not done yet. Every day, we’re channeling our passion and resources into delivering innovative therapies that change the face of healthcare. Let’s outdo yesterday.
• Provide pediatric medical and clinical expertise to support site‑facing discussions related to protocol design, eligibility criteria, safety considerations, and feasibility. • Partner with study clinicians and Global Development Leads to support resolution of complex pediatric clinical questions arising at investigational sites. • Serve as a pediatric medical point of contact for investigator inquiries related to clinical aspects of study conduct, in alignment with protocol and governance. • Partner with the Global Development Leads, Clinical Development Scientist Lead, and study clinicians to execute study‑specific pediatric clinical site engagement activities for IM pediatric programs, with initial focus on the pediatric rimegepant portfolio. • Proactively identify and evaluate pediatric clinical sites (e.g., children’s hospitals and pediatric research networks) to support study feasibility and enrollment needs. • Drive U.S.‑based pediatric site engagement (virtual and face‑to‑face) to improve site readiness and performance. • Accelerate site startup by working directly with sites and internal startup teams to resolve feasibility, documentation, and activation barriers. • Optimize recruitment at activated sites through hands‑on performance support and targeted intervention for underperforming sites. • Provide rapid, field‑informed issue resolution for site problems that threaten screening or randomization momentum, escalating to appropriate operational owners as needed. • Maintain productive working relationships with pediatric investigators and institutions to support site engagement and enrollment delivery. • Serve as a pediatric clinical development partner to study teams, providing site‑facing pediatric medical expertise to support protocol interpretation and practical implementation. • Facilitate bidirectional communication of actionable site insights (e.g., barriers, opportunities, operational pain points) to inform study execution and risk mitigation. • Represent Internal Medicine Clinical Development in the pediatric site community through credible scientific and medical exchange in support of study delivery.
• Medical degree (MD or DO) with 4 years+ relevant experience • Completion of pediatric residency training and/or subspecialty training relevant to pediatric populations • Active or prior medical licensure preferred. • Clinical experience caring for pediatric patients in academic or hospital-based settings. • Experience serving as an investigator, sub-investigator, or medical monitor in pediatric clinical trials. • Extensive experience supporting pediatric clinical research, which may include a combination of biopharmaceutical industry experience, pediatric clinical practice, and/or direct involvement in pediatric clinical trials. • Pediatric subject matter expertise, including experience working with children’s hospitals, pediatric investigators, and pediatric research networks. • Experience supporting pediatric trial feasibility, site identification, site startup, and recruitment execution, with a strong understanding of the unique operational, ethical, and practical considerations of conducting clinical trials in children and adolescents. • Working knowledge of pediatric regulatory frameworks and expectations (e.g., PREA, PWR, PIP) and their implications for study design, execution, and delivery timelines. • Ability to engage credibly as a peer clinical partner with pediatric investigators and site clinicians through scientific and medical exchange. • Ability to operate independently with sound clinical and operational judgment across complex, matrixed development environments. • Success in a field-based or highly autonomous role not anchored to a corporate office, requiring independent prioritization across multiple pediatric studies, travel planning, and execution across geographically distributed clinic in the pediatric site community and operating independently in a field-based environment.
• 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
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