Pediatric Clinical Development Director Lead (Non-MD)

Pfizer • USA - FL - Remote, FL

1d • $214,900 - $358,100 • Remote

About The Position

The Pediatric Clinical Development Director Lead (Internal Medicine, Field‑Based) is a Senior Director–level, field‑based clinical development leadership role within Internal Medicine, operating independently of any Pfizer office location. The position is designed to support pediatric clinical programs through direct engagement with pediatric investigators, children’s hospitals, and research institutions across the United States, with geographic placement determined by field coverage needs rather than office proximity. The role is accountable for both hands‑on pediatric clinical site engagement and leadership of a small team of Pediatric Clinical Development Directors to enable timely and successful delivery of Internal Medicine pediatric clinical programs, with initial emphasis on the pediatric rimegepant portfolio. The role functions as a working Pediatric Clinical Development Director, personally engaging with pediatric investigators, children’s hospitals, and study teams to accelerate site activation, optimize recruitment performance, and resolve site‑level issues that threaten enrollment timelines. In parallel, the role provides senior leadership and accountability for the pediatric site engagement capability within Internal Medicine, including prioritization across studies, performance oversight, coaching and development of team members, and escalation of delivery risks to IM Clinical Development leadership. As a Senior Director and pediatric SME, the Pediatric Clinical Development Director Lead partners closely with the Global Development Leads, Clinical Development Scientist Lead, study clinicians, and Clinical Operations to translate field‑based pediatric insights into actionable execution strategies, risk mitigation plans, and continuous improvement of pediatric site engagement practices.

Requirements

• Doctoral-level degree in a scientific or pharmaceutical discipline (e.g., PhD, PharmD), with demonstrated pediatric clinical trial experience.

Nice To Haves

• ≥10 years of biopharmaceutical industry experience, including pediatric clinical trials, with demonstrated success in direct clinical execution and providing senior leadership, organizational navigation, and influence across cross‑functional development teams.
• Pediatric subject matter expertise, including experience working directly with children’s hospitals, pediatric investigators, and pediatric research networks.
• Experience functioning as a player‑coach, balancing hands‑on individual contributor responsibilities with leadership of a small, specialized team.
• Strong working knowledge of pediatric regulatory frameworks and expectations (e.g., PREA, PWR, PIP) and their implications for trial execution.
• Ability to thrive in a field‑based environment and operate with a high degree of autonomy.
• Experience managing and developing small, highly specialized teams, including goal setting, coaching, and performance management input in a matrixed environment.
• Success in a field‑based or highly autonomous role not anchored to a corporate office, requiring independent prioritization, travel planning, and execution across geographically distributed clinical sites.
• Experience leading, developing, and evolving a specialized clinical development capability or team within a matrixed biopharmaceutical organization.

Responsibilities

• Serve as a hands‑on Pediatric Clinical Development Director for assigned IM pediatric studies, providing direct site‑facing pediatric expertise to investigators and site teams.
• Personally lead pediatric site engagement activities (virtual and face‑to‑face), including site identification, feasibility discussions, start‑up acceleration, and recruitment optimization.
• Work directly with pediatric sites to identify and resolve operational and recruitment barriers (e.g., workflow constraints, competing trials, referral pathway challenges), escalating issues through appropriate operational channels as needed.
• Provide real‑time, field‑based intelligence (e.g., site performance, barriers, competitive dynamics) to study teams to inform execution decisions and risk mitigation strategies.
• Support protocol interpretation and practical implementation at the site level, in partnership with study clinicians and clinical development colleagues, without displacing formal clinical accountability.
• Maintain productive working relationships with pediatric investigators and institutions to support site engagement and enrollment delivery.
• Provide senior leadership and accountability for a small team of Pediatric Clinical Development Directors functioning as a player‑coach.
• Set priorities and guide deployment of pediatric site engagement resources across IM pediatric studies based on dynamic prioritization of delivery risk, enrollment needs, and program timelines.
• Provide performance management input, coaching, and development for Pediatric Clinical Development Directors, fostering consistent execution, professional growth, and pediatric SME excellence.
• Ensure consistency of approach and best practices across pediatric site engagement activities, including site qualification criteria, engagement tactics, escalation pathways, and documentation of lessons learned.
• Provide cross‑study oversight of pediatric site performance, identifying systemic risks and opportunities across IM pediatric programs and driving corrective actions in partnership with Clinical Operations and Global Development Leads.
• Monitor and review performance metrics (e.g., time‑to‑activation, enrollment acceleration, issue resolution cycle time) and synthesize insights for IM Clinical Development leadership.
• Escalate material delivery risks related to pediatric site performance and recruitment to appropriate IM Clinical Development leadership forums, with clear recommendations.
• Partner closely with the Global Development Leads, Clinical Development Scientist Lead, and study clinicians to align pediatric site engagement strategy with overall study delivery plans.
• Contribute to continuous improvement of pediatric site engagement models, tools, and playbooks to support scalability across future IM pediatric programs.
• Support internal decision‑making regarding resourcing, prioritization, and potential expansion of pediatric site engagement capabilities based on evidence and outcomes.
• Operate as a fully field‑based clinical development role, with primary work conducted through direct engagement with pediatric investigators and clinical trial sites.
• Manage travel, scheduling, and prioritization autonomously to align with pediatric site and program demands.

Benefits

• 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
• Relocation assistance may be available based on business needs and/or eligibility.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Ph.D. or professional degree