Medical Director, Clinical Development, Immunology

GSK

Medical Director for clinical development in food allergy at GSK. Supporting late-stage clinical studies and leading cross-functional teams to deliver high-priority programs.

Posted 7/22/2026full-timeMassachusetts, Pennsylvania • 🇺🇸 United StatesLead💰 $222,750 - $371,250 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical drug development and trial execution, with a strong focus on clinical research methodology and regulatory compliance. Capable of effective medical oversight and protocol design, ensuring alignment with strategic goals and patient safety.

Highest-signal resume keywords

Medical DegreeClinical Drug DevelopmentClinical Research MethodologyICH GuidelinesFDA Requirements

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ExecutionInterventional Study DesignMedical MonitoringData ReviewProtocol DesignClinical Endpoint SelectionPatient Population StrategyBiostatistical PrinciplesEvidence GenerationRegulatory Interactions

Soft Skills

MentoringCollaborationInfluencingCommunicationLeadership

Certifications & Qualifications

Clinical Medical Specialty Training Board Qualification

Industry Keywords

Integrated Evidence PlanClinical Development PlanIgE Mediated DiseaseFood AllergyRegulatory CompliancePatient SafetyCommercial GoalsStudy DeliveryDecision PointsMatrix Team Collaboration

Tech Stack

Tools & technologies

About the role

Key responsibilities & impact

Supporting the strategic management of the Integrated Evidence Plan (IEP), including the Clinical Development Plan (CDP) for asset(s) in development
Ensuring alignment with and support of project strategic plans, regulatory requirements, and commercial goals, optimizing clinical study design aligned with IEP and CDP
Generating the data and evidence required to determine a medicine’s potential efficacy, safety profile, key areas of product differentiation, and value to patients.
Providing effective support and oversight of evidence generation activities to assure patient safety and study delivery.
Enabling robust protocol design, including selection of clinical endpoints, patient populations, and participant monitoring strategy
Working with Clinical Operations and Biostatics to deliver clinical development timelines, enabling key decision points and Go/No Go criteria for the CDP
Active medical monitoring activities and medical data review of ongoing studies, including: Lead, coordinate activities and present at IDMCs, adjudication committees, ongoing routine safety review
Interpretation and presentation of clinical data for clinical study reports and publications
Oversee and train study team on protocol-related activities in collaboration with matrix study team members
Developing and maintaining relationships with program counterparts, including Commercial, Research, Regulatory, Clinical Operations, and Statistics
Interfacing and influencing a diverse range of scientific external experts (e.g., regulators, payors, CROs, consultants, investigators) in order to deliver clinical programs, align to business strategy, and address patient needs.
Gathering and supporting the integration of inputs from across disciplines (scientific, clinical, commercial, regulatory) to contribute to clinical components of the Medicine Profile
Contributing to regulatory interactions including briefing documents, presentations, addressing questions and responses
Serving as a clinical representative for senior management and senior level matrix teams, both internally and externally for an asset in development
Contributing to the implementation and embedding of strategic initiatives and various organizational initiatives in RIIRU
Supporting technical and leadership development of RIIRU staff via mentoring and coaching for matrix team members
Support enterprise efforts to streamline and grow efficiencies for the business unit

Requirements

What you’ll need

Medical degree and clinical medical specialty training board qualification/registration in Internal Medicine or Primary Care/Family Medicine with specialized experience in IgE mediated disease and food allergy.
Experience in clinical drug development, with experience of clinical trial execution from concept to publication.
Clinical research experience in food allergy, including clinical development planning and interventional study design.
Experience with in‑stream medical oversight activities during trial conduct.
Experience with ICH guidelines, FDA requirements, and global regulatory expectations.
Experience in clinical research methodology and biostatistical principles to support innovative and efficient clinical trial design and data‑driven decision rules.

Benefits

Comp & perks

health care and other insurance benefits (for employee and family)
retirement benefits
paid holidays
vacation
paid caregiver/parental and medical leave