Future Tech Jobs
Future Tech Jobs
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...
This role involves driving adoption of respiratory biologics within secondary care settings by building strategic relationships with multi-disciplinary teams and key healthcare stakeholders. The Account Manager will lead formulary access, support homecare utilization, and execute account plans in a complex clinical environment. It requires strong commercial acumen, deep understanding of the NHS ecosystem, and the ability to navigate multi-stakeholder decision-making units.
This role involves leading CSL's presence in key innovation hubs across Northern Europe and the UK, building strategic partnerships, and driving business development. The Director will maintain relationships with universities, incubators, and venture capital firms, and actively participate in industry events to enhance CSL's external brand and deal flow.
This role involves leading CSL's presence in key innovation hubs across Northern Europe and the UK, building strategic relationships with biotech, academia, and investment networks. The Director will source and evaluate opportunities, lead deal teams, and represent CSL at industry events to enhance the company's reputation and deal flow.
The Director of Biostatistics leads the statistical aspects of clinical development programs, ensuring robust study design, data analysis, and regulatory submissions. They collaborate closely with cross-functional teams and regulatory authorities to drive the success of clinical trials and therapeutic programs.
The Director of Biostatistics leads the statistical aspects of clinical development programs, ensuring robust data analysis and regulatory compliance. They collaborate with cross-functional teams, manage external partners, and represent Biostatistics in regulatory interactions.
The Director of Biostatistics leads the statistical aspects of clinical development programs, ensuring robust study design, data analysis, and regulatory submissions. They collaborate closely with cross-functional teams and regulatory authorities to drive the success of clinical trials and ensure high-quality statistical insights.
This role involves leading cross-functional teams in reviewing safety data, mentoring junior staff, and ensuring compliance with GxP guidelines and international regulations. The position also focuses on managing pharmacovigilance procedures, conducting impact assessments of new legislation, and supporting regulatory inspections and audits.
This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic area opportunities, from Phase 2 through marketed drugs. Responsibilities include engaging with Key Opinion Leaders, driving due diligence, and shaping the portfolio through high-impact partnerships.
This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic assets, engaging with key opinion leaders, and integrating innovation priorities into portfolio planning. The position requires deep clinical expertise and a proven track record in business development and deal-making.
This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic assets, engaging with key opinion leaders, and integrating innovation into portfolio planning. The position requires deep clinical expertise, a proven track record in deal-making, and strong collaboration with cross-functional teams.
This role leads the establishment and maintenance of processes and standards across CSL's global Portfolio Development function, ensuring high-quality clinical trial planning, evaluation, and reporting. The Director will drive process improvement, SOP governance, training curriculum development, and cross-functional change initiatives within a dynamic biotech R&D environment. They will work closely with leadership and international teams to reduce complexity, improve quality and speed, and align procedural frameworks across clinical development, biomarkers, and commercial operations.
Lead global regulatory project planning and execution across CSL’s product portfolio, ensuring timely submissions and alignment with strategic initiatives. Oversee cross-functional teams, drive process improvements, and ensure compliance with global health authority requirements. Mentor junior staff and contribute to governance and standardization in regulatory operations.
Leads global regulatory project planning and execution across CSL’s product portfolio, overseeing submission coordination and cross-functional collaboration to meet health authority requirements. Drives process improvements and operational excellence within regulatory operations, aligning initiatives with strategic priorities. Mentors junior staff and supports standardization of regulatory processes across regions.
This role leads global regulatory project planning and execution across CSL’s biologics product portfolio, overseeing end-to-end regulatory submissions and cross-functional collaboration. The individual will manage project timelines, risk, and compliance while driving process improvements and mentoring junior staff. Work involves close coordination with regulatory, clinical, manufacturing, and policy teams to meet global health authority requirements.
