Associate Director, Hematology

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.The Associate Director in Translational Research Hematology is responsible for the design, execution, and oversight of translational and non-interventional biomarker studies, with a focus on understanding disease mechanisms, target validation, and biomarker discovery. This role plays a pivotal part in bridging preclinical research and clinical development by applying scientific expertise to support therapeutic area (TA) strategies,. The position includes scientific leadership, cross-functional collaboration, especially with Pre-clinical Pharmacology, Clinical Pharmacology, Data Science and Early Clinical Development functions, and strategic input into global research and development initiatives.Main ResponsibilitiesDesign, implement, and oversee translational and non-interventional biomarker studies, including protocol development in the fields of Hematology including data analysis, and quality assuranceContribute to biomarker strategies for toxicology and early clinical studies, by fully leveraging all elements for generation of Integrated Translational Evidence, i.e systematic literature reviews, integration of real-world data/evidence, insights gained from post-hoc studies and from prospective, non-interventional research studies (NIRS)Lead and support mechanism of action studies, biomarker discovery and development, and target validation using in vitro, ex vivo, and in vivo models, working closely with the internal Pharmacology Unit or external partners/vendors to access lab capabilities (e.g., academic institutions, biotech companies)Provide scientific and operational guidance to R&D projects across preclinical and clinical phasesRepresent TR in TA Research core teams and RPTs; closely liaise with RTALs to support research strategiesRepresent Translational Research in global cross-functional teams, such as PSTs, NCETs and BETs, working closely with pre-clinical Pharmacology, Clinical Bioanalytics and Biomarkers, Clinical Pharmacology, Data Science and Early Clinical Development functionsContribute to regulatory submissions, investigator brochures, and scientific publicationsSupervise and mentor research scientists (e.g. from internal Pharmacology Units ), ensuring delivery of TA-aligned research packagesMaintain state-of-the-art knowledge through literature review and participation in scientific meetingsSupport contract negotiations and patent filings in collaboration with legal teamsEnsure compliance with quality standards and contribute to the maintenance of the QM systemProvide input into strategic planning and due diligence processes for early-phase projectsQualifications and Experience RequirementsPhD, MD-PhD or equivalent in a relevant discipline (e.g., Biochemistry, Cell Biology, Immunology, Molecular Biology, Epidemiology), specific expertise in diseases relevant to CSL’s TA Strategies is a prerequisiteMinimum of 8–10 years of relevant experience in industry and/or academia, with a strong track record in translational researchProven expertise in biomarker discovery, non-interventional study design, and translational biologyExperience in integrating clinical and scientific data to inform hypothesis generation and clinical developmentStrong knowledge of epidemiological and statistical methods applied to translational and observational studiesDemonstrated leadership and people management skills in a matrixed, cross-functional environmentExcellent communication, analytical, and strategic thinking skillsExperience in regulatory documentation, scientific writing, and external collaborationsAbility to work effectively in multicultural and international teamsAre you interested? We are looking forward to receiving your online application.About CSL PlasmaCSL Plasma operates one of the world’s largest and most sophisticated plasma collection networks, with over 350 plasma collection centers in the U.S., Europe and China. Headquartered in Boca Raton, Florida, CSL Plasma is a subsidiary of CSL Behring, a global biotherapeutics business and a member of CSL. Plasma collected at CSL Plasma facilities is used by CSL Behring for the sole purpose of manufacturing lifesaving plasma-derived therapies for people in more than 100 countries. The parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people.Learn more about CSL Plasma here and CSL, CSL Behring, CSL Seqirus and CSL Vifor here Learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor here at and CSL Plasma atOur BenefitsFor more information on CSL Plasma benefits visitYou Belong at CSLAt CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.To learn more visit Equal Opportunity EmployerCSL 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