Senior Clinical Scientist

Position Overview The Senior Clinical Scientist will be a key member of a clinical development team supporting protocol development and study delivery. The position holder works closely with the CDT Lead and other Clinical Representatives in performing delegated tasks in support of the clinical development program as dictated by therapeutic area/ project needs. Relocation assistance and visa sponsorship are not provided

Key Responsibilities
Under general direction, contributes to the scientific development of individual clinical studies in alignment with the approved clinical development plan Provides scientific input for the safe, efficient, and timely execution of assigned programs, ensuring the highest quality and full compliance of all outputs Contributes to the development of program and core clinical development documents and training materials aligned with the scientific strategy (e.g. clinical development plan, IB, protocols, eCRF, ICF, study reference manuals, investigator trainings) Reviews clinical data with some assistance and assists with interpreting data from clinical studies, and writing/editing or reviewing results in study reports, regulatory submissions, abstracts, posters, presentations, peer reviewed manuscripts, and other documents Supports medical monitoring and oversight of individual clinical studies to ensure the highest level of patient safety and data integrity Steering committee, independent data monitoring committee, adjudication committee) Minimum Qualifications Bachelor’s degree, or equivalent, in a Life Sciences discipline is required An advanced degree (MS, PhD) in a Life Sciences discipline is highly preferred PhD with 3+ years/ MS with 4+ years or BS with 5+ years of clinical research/clinical development experience in the biotechnology or pharmaceutical industry The successful candidate will have a strong scientific framework, coupled with ability to work towards tangible outcomes, meeting timelines and ensuring study delivery Experience with contributing to multidisciplinary working groups to support continuous process improvement as requested Builds bridges and helps teams develop collaboration Ignites agility and instills personal flexibility in self and teams In addition to base salary, total compensation for this role may also include incentive compensation and equity. #Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. Our Benefits For more information on CSL benefits visit How CSL Supports Your Well-being | CSL. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. To learn more about inclusion and belonging visit If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit CSL is an Equal Opportunity Employer. If you are an individual with a disability and need any reasonable accommodation for any part of the application process click here…