Executive Medical Director leading clinical development strategies for food allergy assets at GSK. Collaborating with cross-functional teams to enhance health outcomes and ensure successful drug delivery.
Responsibilities
Work with medicine teams to plan and assure delivery of clinical research and development activities
Work with early development teams to plan clinical development programs and establish efficient collaboration enabling seamless transition from early to late phase of development
Lead the end-to-end clinical development strategy for a drug or program.
Manage specific clinical development plans for product(s) and/or indication(s) in specific therapy/disease areas
Contribute to the strategic management of the Integrated Evidence Plan (IEP), including oversight of the Clinical Development Plan (CDP) and its component clinical trials for an asset in development.
Be accountable for the clinical components of the Target Medicine Profile (TMP)
Provide strategic leadership, for example in assuring that the clinical study designs are aligned with the IEP and CDP, and consider the scientific rationale, regulatory requirements, product development plan and commercial goals
Establish and deliver to clinical development timelines, enabling key decision points and Go/No Go criteria for the CDP
Develop and maintain relationships with program counterparts in Commercial, Research, Regulatory, Clinical Operations and Statistics
Serve as a clinical point of contact for senior management and senior level matrix teams
Contribute to the strategic and organizational initiatives in Clinical Development
Contribute to Business Development activities, including due diligence projects
Support technical and leadership development of Clinical Sciences staff via direct line management, mentoring and coaching
Interface with and influence a range of scientific external experts (e.g., regulators, payors, CROs, subject matter consultants, investigators) to deliver clinical programs that align to our business strategy and address patient needs
Lead and be accountable for the evaluation of the probability of technical success (PTS) of clinical studies/programs
Identify and highlight transformational opportunities where projects can offer highly significant benefit to patients
Assess benefit/risk at the study and/or project level. Take action to mitigate risk where appropriate
Make substantial contributions to global regulatory interactions and files, including briefing documents, presentations, submission documents, and responses to questions
Champion implementation of innovative methods and processes within clinical development and gains stakeholder support; encourages others to think differently and produce business solutions
Requirements
Medical Degree with specialist training or board qualification/eligibility in Allergy and Immunology.
Experience in (bio-)pharmaceutical industry experience in food allergy clinical drug development
Experience with planning clinical development for an asset and/or indication. Proven record of delivery of clinical trials and projects
Experience of clinical research methodology and principles of biostatistics to facilitate innovative and efficient designs of clinical trials and clinical development plans with clear data-driven decision rules
Line/matrix management experience
Benefits
health care and other insurance benefits (for employee and family)
retirement benefits
paid holidays
vacation
paid caregiver/parental and medical leave
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