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Global Clinical Program Lead, Immunology
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Healthcare Medical
💰 Salary 24,005 GBP–36,007 GBP/mo (288,059 GBP–432,088 GBP/yr)
📊 Market 16,667 GBP–29,167 GBP/mo (200,004 GBP–350,004 GBP/yr)
About the Company
AZ's vision is to grow and expand the indications and assets in immunology to become a major player in the field. With one of the broadest and deepest pipelines, we are determined to keep contributing and pushing forward.
About the Role
This Global Clinical Program Lead (GCPL) role in Late stage clinical development in Immunology is designed to help deliver on that ambition. As GCPL in Gastroenterology, you will provide medical and scientific input into programs of small molecules, biologics or cell therapy for clinical stage assets and provide program leadership that is passionate about gastroenterology and clinical immunology.
Responsibilities
- ● You will take responsibility for clinical development in cross-functional teams to support early to late phase clinical development activities.
- ● You will be responsible for study design concept delivery.
- ● You will drive clinical and scientific decisions within Global Study Team remits together with other team members.
- ● You will be accountable for clinical, scientific, and ethical components of studies including patient safety on a study and/or program level in compliance with Good Clinical Practice.
- ● You will be accountable for scientific medical input to all relevant study documents to ensure consistency within clinical program and alignment with scientific rationale.
- ● You will be accountable for scientific medical content at international investigator meetings, and support to local Marketing Companies for country level activities.
- ● You will be accountable for safety surveillance on a study level and/or program level including the process for Adverse Events reporting.
- ● You will review the Clinical Study Report and play a key role in preparation and production of relevant sections.
- ● You will be accountable for induction and education of new Global Study Team members.
- ● You will work with GCH and TA leadership for identifying risks and proposing mitigation strategies to deliver successful phase IIb, III, IV or Life Cycle Management studies.
- ● You will deliver clinical, scientific, and medical information/query responses to Regulatory Agencies, Ethic Committees, Marketing Companies, and investigators/sites, and provide clarifications as well as solve clinical, scientific, and medical issues in the Global Study Team.
Application Notes
Make a more meaningful contribution. Impact patients' lives every day. Join a place with the commitment, knowledge and backing from the business to continue expanding our pipeline. When we get it right there's nothing more motivating.
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