Director, Non-clinical Pharmacology CVR at CSL

, , Switzerland -

Full Time

Start Date

Immediate

Expiry Date

08 Feb, 26

Salary

0.0

Posted On

10 Nov, 25

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Pharmacology, Physiology, Biomedical Sciences, In Vivo Pharmacology, Disease Models, Translational Science, Regulatory Expectations, Project Management, Problem Solving, Communication, Interpersonal Skills, Cardiovascular Biology, Renal Biology, Scientific Leadership, Team Leadership, Data Analysis

Industry

Pharmaceutical Manufacturing

Description

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. We are seeking a Therapeutic Area (TA) Pharmacology Lead (Transplant & Immunology) to drive the design, execution, and interpretation of in vivo pharmacology studies that support drug discovery and development. This role is pivotal in characterising the pharmacological profile of novel therapeutic candidates through internal studies and external collaborations. Main Responsibilities Scientific Leadership Define and lead the nonclinical pharmacology strategy for discovery and development programs within the relevant therapeutic area (Cardiovascular and/or Renal) Design and oversee in vivo efficacy, pharmacodynamic (PD), and mechanism-of-action studies in relevant animal models. Guide the selection and validation of disease models that best represent human pathophysiology. Study Design & Execution Develop and implement study protocols for pharmacology, target engagement, and biomarker evaluation. Select external collaborators or CROs and collaborate with internal teams, academic collaborators or CROs to ensure high-quality and timely execution of pharmacology studies. Analyze and interpret complex data sets to inform compound progression and candidate selection. Cross-Functional Collaboration Act as Sr. Pharmacology lead on TA teams. Work closely with PK, Toxicology, Translational Science, to integrate pharmacology data into broader development plans. Participate in project teams and TA-teams and provide expert input on pharmacology-related issues. Provide expert input into due diligence for in-licensing or partnership opportunities. Documentation & Communication Prepare study reports, presentations, and regulatory documents (e.g., IND, CTA). Present findings to internal stakeholders and external collaborators as needed. Team Leadership: Lead and mentor a team of Principal and Sr. scientists, incl. in-vivo lab work. Foster a culture of scientific excellence, innovation, and continuous learning. Qualifications and Experience Requirements: Ph.D. in Pharmacology, Physiology, Biomedical Sciences, or a related field. 10+ years of experience in nonclinical pharmacology within the pharmaceutical or biotech industry or academic background with proven and deep understanding of pharmaceutical development Strong expertise in in vivo pharmacology, disease models, and translational science for the relevant TA (Cardiovascular and/or Renal Disease Biology). Familiarity with regulatory expectations for nonclinical pharmacology data. Proven ability to manage multiple projects and timelines. Strategic thinker with excellent problem-solving, communication, and interpersonal skills. Experience across multiple therapeutic areas and modalities is highly desirable Extensive knowledge in one of Cardiovascular or Renal Biology is essential; both would be viewed highly favorably. Are you interested? We are looking forward to receiving your online application. Our Benefits We encourage you to make your well-being a priority. It’s important and so are you. Learn more about how we care at CSL. About CSL Behring CSL Behring is a global biotherapeutics leader driven by our promise to save lives. 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. We want CSL to reflect the world around us 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. 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. Learn more Inclusion and Belonging | CSL. Do work that matters at CSL Behring! 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 click here. CSL Global Privacy Notice for Job Applicants and Candidates

Responsibilities

The role involves defining and leading the nonclinical pharmacology strategy for drug discovery and development programs, as well as designing and overseeing in vivo pharmacology studies. The position requires collaboration with cross-functional teams and external partners to ensure the successful execution of pharmacology studies.