Portfolio Director

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives 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 Director, Portfolio Development Process & Standards Lead? This position is located in our King of Prussia, PA; Waltham, MA; or Maidenhead, UK office. It is a hybrid role, three days onsite. You will report to the Head, Portfolio Development Excellence, Process & Compliance. Responsibilities Establish and maintain a framework that allows the Global Portfolio Development group, in collaboration with partner functions, to plan, evaluate, and report clinical trials and programs under the highest quality standards. Manage all Portfolio Development (CD/BM/CO) owned SOP updates in collaboration with critical partner SMEs and ensure they are updated to reflect current processes and structure. Drive development of a fit-for-purpose technical training curriculum across Portfolio Development, supporting the achievement of quality program goals and standards. Provide guidance on process and procedural expectations and stakeholder management. Track and manage all Portfolio Development sponsored process development and improvement initiatives, collaborating with delegates, surfacing to the Portfolio Development Chief of Staff, and identifying cross‑functional initiatives to incorporate technology. May sponsor or lead cross‑functional initiatives supporting design and execution excellence. Track and manage all procedural document update requirements to ensure compliance across the department in collaboration with the Portfolio Development Leadership Team and appropriate delegates. Provide innovative solutions to increase the excellence of Portfolio Development; aim to reduce complexity, increase quality and speed, and reduce decision‑making churn. Represent Portfolio Development for applicable cross‑functional R&D initiatives and forums. Act as core reviewer on all Portfolio Development SOP updates to ensure changes work systematically across procedural documents. Qualifications Bachelor’s degree or equivalent in life sciences, nursing, pharmacy, medical laboratory technology, or another health/medical related area preferred; other degrees and certifications are considered if commensurate with related clinical research experience. 12+ years of experience in the biotechnology or pharmaceutical industry, or a biomedical research organization. In‑depth knowledge of drug development and GCP environment. 5+ years of experience managing projects in Clinical Research and Development, with first‑hand experience in the execution of clinical trials required. 3+ years of experience managing process improvement initiatives and influencing change in an organization. Proven experience leading cross‑functional, multicultural, and international product development teams. Benefits The expected base salary range for this position at hiring is $230,000 – $270,000. In addition to base salary, total compensation may also include incentive compensation and equity. Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit #J-18808-Ljbffr