Associate Director, Clinical Pharmacology
Denali Therapeutics Inc., South San Francisco, California, us, 94083
Associate Director, Clinical Pharmacology page is loaded## Associate Director, Clinical Pharmacologylocations:
South San Franciscotime type:
Full timeposted on:
Posted 4 Days Agojob requisition id:
R-1463Neurodegenerative diseases are one of the largest medical challenges of our time. Denali Therapeutics is a biotechnology company dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles of translational medicine. Denali is founded on the collaboration of leading scientists, industry experts, and investors who share the vision that scientific discovery energetically applied to translational medicine is the key to delivering effective therapies to patients.We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients.The Associate Director in Clinical Pharmacology will develop and lead clinical pharmacology and modeling and simulation (M&S) strategies for biotherapeutic and small molecule programs, and guide project teams from early development through late-stage clinical trials and regulatory submissions. This role involves designing and executing clinical studies, analyzing pharmacokinetic (PK)/pharmacodynamic (PD) data, and leading and collaborating with cross-functional teams to advance therapies for neurodegenerative diseases. This role is within the Quantitative and Clinical Pharmacology (QCP) team in the Development Sciences function.**Key Accountabilities/Core Job Responsibilities:*** Independently develop and lead Clinical Pharmacology and M&S strategies for multiple biotherapeutics and small molecule programs from pre-IND through late-stage clinical studies, including pivotal Phase 2/3 trials and NDA/MAA/BLA submissions.* Develop and review clinical study designs and write study protocols, amendments, and reports that meet regulatory standards and project timelines.* Lead and conduct hands-on advanced pharmacokinetic (PK) and pharmacodynamic (PD) data analysis using advanced tools and methodologies to support clinical decision-making.* Analyze, interpret, and communicate PK/PD data to project teams, senior leadership and management, regulatory authorities, and external conferences.* Author and review sections of regulatory submissions, including IND/CTA and NDA/MAA/BLA filings.* Mentor and/or manage junior team members fostering their professional development and contributing to team growth.* Lead direct report(s), where applicable, through annual goal setting, growth planning,adherence to company policies, maintain training compliance and provide ongoing feedback on growth, development and areas of improvement.* May manage external vendors as needed.**Qualifications/Skills:*** PhD or PharmD, or other advanced degree, in Pharmaceutical Sciences, Pharmacology, Pharmacokinetics, or a related scientific discipline.* At or near 7 years of relevant work experience inclusive of postdoctoral work; or MS with 10+ years of relevant work experience.* Strong understanding of PK/PD principles and regulatory expectations across all phases of development.* Hands-on experience with quantitative analysis tools such as Phoenix WinNonlin, NONMEM, or similar software.* Demonstrated success leading clinical pharmacology components of global development programs.* Excellent written and verbal communication skills, with ability to present complex data to technical and non-technical audiences.* Proven track record of collaboration within cross-functional drug development teams.* Experience in neuroscience, rare disease, or biotherapeutics development preferred.Salary Range: $188,000.00 to $283,000.00 .
Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Denali offers a competitive total rewards package, which includes a 401k, healthcare coverage, ESPP and a broad range of other benefits. Learn more at https://www.denalitherapeutics.com/careersThis compensation and benefits information is based on Denali’s good faith estimate as of the date of publication and may be modified in the future.This compensation and benefits information is based on Denali’s good faith estimate as of the date of publication and may be modified in the future.Denali is committed to its core company value of unity by creating a diverse and inclusive environment. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state, or local protected class.“Life at Denali” is a living reflection of our values: trust, unity, grit and growth. These are not just words we share—they shape how we show up, collaborate and push boundaries together. From the lab to the community, across functions and milestones, our culture thrives on shared purpose and relentless pursuit. #J-18808-Ljbffr
South San Franciscotime type:
Full timeposted on:
Posted 4 Days Agojob requisition id:
R-1463Neurodegenerative diseases are one of the largest medical challenges of our time. Denali Therapeutics is a biotechnology company dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles of translational medicine. Denali is founded on the collaboration of leading scientists, industry experts, and investors who share the vision that scientific discovery energetically applied to translational medicine is the key to delivering effective therapies to patients.We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients.The Associate Director in Clinical Pharmacology will develop and lead clinical pharmacology and modeling and simulation (M&S) strategies for biotherapeutic and small molecule programs, and guide project teams from early development through late-stage clinical trials and regulatory submissions. This role involves designing and executing clinical studies, analyzing pharmacokinetic (PK)/pharmacodynamic (PD) data, and leading and collaborating with cross-functional teams to advance therapies for neurodegenerative diseases. This role is within the Quantitative and Clinical Pharmacology (QCP) team in the Development Sciences function.**Key Accountabilities/Core Job Responsibilities:*** Independently develop and lead Clinical Pharmacology and M&S strategies for multiple biotherapeutics and small molecule programs from pre-IND through late-stage clinical studies, including pivotal Phase 2/3 trials and NDA/MAA/BLA submissions.* Develop and review clinical study designs and write study protocols, amendments, and reports that meet regulatory standards and project timelines.* Lead and conduct hands-on advanced pharmacokinetic (PK) and pharmacodynamic (PD) data analysis using advanced tools and methodologies to support clinical decision-making.* Analyze, interpret, and communicate PK/PD data to project teams, senior leadership and management, regulatory authorities, and external conferences.* Author and review sections of regulatory submissions, including IND/CTA and NDA/MAA/BLA filings.* Mentor and/or manage junior team members fostering their professional development and contributing to team growth.* Lead direct report(s), where applicable, through annual goal setting, growth planning,adherence to company policies, maintain training compliance and provide ongoing feedback on growth, development and areas of improvement.* May manage external vendors as needed.**Qualifications/Skills:*** PhD or PharmD, or other advanced degree, in Pharmaceutical Sciences, Pharmacology, Pharmacokinetics, or a related scientific discipline.* At or near 7 years of relevant work experience inclusive of postdoctoral work; or MS with 10+ years of relevant work experience.* Strong understanding of PK/PD principles and regulatory expectations across all phases of development.* Hands-on experience with quantitative analysis tools such as Phoenix WinNonlin, NONMEM, or similar software.* Demonstrated success leading clinical pharmacology components of global development programs.* Excellent written and verbal communication skills, with ability to present complex data to technical and non-technical audiences.* Proven track record of collaboration within cross-functional drug development teams.* Experience in neuroscience, rare disease, or biotherapeutics development preferred.Salary Range: $188,000.00 to $283,000.00 .
Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Denali offers a competitive total rewards package, which includes a 401k, healthcare coverage, ESPP and a broad range of other benefits. Learn more at https://www.denalitherapeutics.com/careersThis compensation and benefits information is based on Denali’s good faith estimate as of the date of publication and may be modified in the future.This compensation and benefits information is based on Denali’s good faith estimate as of the date of publication and may be modified in the future.Denali is committed to its core company value of unity by creating a diverse and inclusive environment. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state, or local protected class.“Life at Denali” is a living reflection of our values: trust, unity, grit and growth. These are not just words we share—they shape how we show up, collaborate and push boundaries together. From the lab to the community, across functions and milestones, our culture thrives on shared purpose and relentless pursuit. #J-18808-Ljbffr