# Director, Global Clinical Program Lead at CSL

CSL is hiring a Director, Global Clinical Program Lead. Level rates it Little AI ●○○○; you can [apply on CSL](https://jobsbylevel.com/go/44467842-e1f6-4d4f-b83c-dabd20baeb8f?utm_medium=ai-agent).

AI Level 1, AI centrality 0 out of 100. EMEA, CH, Glattbrugg, CSL Behring.

## Details

- Company: [CSL](https://jobsbylevel.com/companies/csl)
- AI level: AI Level 1 (score 0 out of 100)
- Location: EMEA, CH, Glattbrugg, CSL Behring
- Posted: November 3, 2026
- Apply: https://jobsbylevel.com/go/44467842-e1f6-4d4f-b83c-dabd20baeb8f?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=director-global-clinical-program-lead-at-csl-8dd03f

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## Description

The Global Clinical Program Leader (GCPL) is a critical role within Clinical Development. The GCPL is accountable for the design and execution of the clinical strategy to support the development of a medicine, aligned with the Project Strategy Document (PSD) and the Target Product Profile (TPP). The GCPL is accountable for the strategic leadership of the Clinical Development Team (CDT) in a matrix environment and is responsible for: the timely development and execution of the Clinical Development Plan (CDP). managing the day-to-day operations of the CDT including but not limited to meeting coordination and documentation, decision making, and stakeholder management. ensuring that the program is conducted in alignment with CSL Behring processes and abiding by GCP and ICH regulations. This position is accountable for the clinical & scientific oversight of the assigned program(s) and: ensures high quality clinical & scientific standards are met during all aspects of the program providing clinical oversight and expertise during development of clinical studies serves as medical monitor for assigned clinical trials or provides oversight to an assigned medical monitor serves as the Clinical Development representative on the Project Strategy Team (PST) serves as the Clinical Development representative, or provides oversight to an assigned representative to cross-functional delivery teams (eg, Study Execution Team, etc.) undefinedThis position is a “Lead Author” or “Contributing Author” for:key study documents, including but not limited to the Clinical Development Plan (CDP), the Project Strategy Document (PSD), Investigator Brochures (IB), Clinical Study Protocols (CSP), Informed Consent Forms (ICF), Medical Monitoring Plans (MMP), Clinical Study Reports (CSR).the clinical sections of relevant regulatory packages (e.g. IND, NDA, annual reports) and support regulatory RFIs as needed.the development of abstracts, presentations, and manuscripts as appropriate. The incumbent may also be assigned as a Business Development (BD) Contributor, or a Clinical Study Lead as appropriate for projects as assigned per business need. Main Responsibilities and Accountabilities: 1. Clinical Development Team (CDT) Leadership: Provides leadership and guidance to all members of the cross-functional CDT acting as the lead scientific expert for the clinical program, while ensuring appropriate functional representation in team discussions. Is accountable for the timely development and maintenance of the Clinical Development Plan (CDP) in alignment with the Program Strategy Team (PST) and Therapeutic Area Leadership Team (TALT). Leads the integration of internal and external expert contributions to strategy and design of the assigned clinical program(s). Responsible for maintaining alignment across critical stakeholders prior to key decision making forums (e.g. Strategic Development Committee (SDC) or Scientific and Technical Review Committee (STRC) for study outline approval). Ensures that the program is conducted in alignment with CSL Behring processes and abiding by GCP and ICH regulations. Responsible for driving and documenting decision making within the CDT, facilitating issue resolution and escalation, as well as contingency planning. 2. Clinical & Scientific Oversight: Accountable for the clinical content for all CDT deliverables to ensure safe, efficient, timely and quality execution of assigned clinical programs. Ensures high quality clinical and scientific standards are met throughout all aspects of the program. Serves as the clinical development representative on the required cross-functional teams, including but not limited to the Study Execution Team (SET), Safety Management Team (SMT), the Benefit-Risk Assessment Team (BRAT), the Biomarker Expert Team (BET), and the Evidence and Access Strategy Team (EAST) for assigned programs. Develops and executes the Medical Monitoring Plan (MMP) strategy. Typically serves as the medical monitor for clinical

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