CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Could you be our next Head of Pharmacovigilance Operations? The job is in our King of Prussia, PA, Waltham, MA or Zurich Switzerland office. This is a hybrid position and is onsite three days a week. You will report to The Director Clinical Scientist Lead for Hematology and Transplant. You will be responsible for scientific input to clinical development strategies, acting as the primary liaison between the assigned therapeutic area and key stakeholders to ensure translation of the development plan into operational deliverables. Contribution to the scientific content of clinical program documents is a key deliverable and includes study synopses and protocols, investigator’s brochures, informed consent forms, clinical study reports, medical monitoring plans, conference abstracts, internal and external scientific meeting presentations, and peer-reviewed publications. Responsibilities: • Provides scientific and clinical development input for the safe, efficient and timely execution of assigned programs, ensuring the highest quality and full compliance of all outputs • Will contribute to the development of the scientific strategy of the clinical development plan, the design and development of trial related documents and the scientific oversight of clinical trials • Facilitates a team to define and deliver the clinical strategy within projects and programs • Defines scientific strategy for various program components • Can lead development of Clinical Development Program • Authors clinical study documents and assists with development/critical review of submission documents • Contributes to au...