Sr. Director, Clinical Pharmacology & Pharmacometrics

Taiho Pharma Canada, Inc.; Pleasanton (CA); On-site; USD 263,500 - 310,000; Full time

Benefits offered by this job

401(k) eligibility

Paid time off benefits

Job summary

Taiho Pharma Canada, Inc. is seeking a Senior Director for Clinical Pharmacology & Pharmacometrics in Pleasanton, CA. This role is pivotal in overseeing pharmacometric activities and collaborating with various departments to enhance drug development processes for oncology compounds.

The ideal candidate will have over 12 years of relevant experience and an advanced degree in a related field, demonstrating strong leadership and communication skills. The compensation ranges between $263,500 and $310,000 annually, along with comprehensive benefits.

Qualifications

• Minimum of 12 years of industry experience focused on clinical development.
• Experience in PK, PK/PD modeling, and oncology clinical trials.
• Ability to analyze and interpret professional journals and data.

Responsibilities

• Develop overall CP strategy for oncology compounds in clinical trials.
• Integrate datasets to optimize dose selection and study designs.
• Collaborate with cross-functional teams to implement modeling solutions.

Skills

Industry experience in oncology

PK/PD modeling knowledge

Leadership experience

Regulatory submissions experience

Education

Doctoral or Ph.D. in pharmacology-related discipline

Tools

Data Management software

MS Office products

Job description

Sr. Director, Clinical Pharmacology & Pharmacometrics

Pleasanton, CA, USA

Position Summary

The Senior Director, Clinical Pharmacology & Pharmacometrics, Modeling and Simulation will be in charge of the clinical pharmacology (CP), pharmacometrics and Modeling & Simulation activities related to oncology compound development for Taiho Oncology, Inc. (TOI).

Performance Objectives

• Develop the overall CP strategy and reporting plans for oncology compounds developed in TOI-sponsored clinical trials by:
  • Writing or overseeing the writing of all CP/PK sections of Phase I–III trials.
  • Reviewing the finalization of all CP/PK-related sections of Statistical Analysis Plans.
  • Develop and execute computational modeling strategies for pharmacometric analyses, including PK/PD modeling, exposure–response modeling, and quantitative systems pharmacology (QSP).
  • Collaborating with Clinical Development, Biostatistics, Clinical Operations and Regulatory to incorporate PK and CP components and activities into the final protocols, clinical study reports and regulatory submission documents.
  • Support regulatory submissions by writing or reviewing clinical pharmacology components of regulatory documents.
• Integrate diverse datasets (clinical trial data, real‑world data, patient characteristics, disease biology) to optimize dose selection, dosing regimens, and study designs.
  • Curate, visualize, and manage large, complex datasets from multiple sources.
  • Integrate pharmacometric workflows using modern data architecture, data science engineering, and advanced computing.
  • Collaborate with cross‑functional teams (clinical pharmacology, pharmacometrics, regulatory, data science) to implement modeling solutions.
  • Academic publications, including scientific meeting abstracts and peer‑reviewed articles.
  • Mentor and lead junior scientists in quantitative modeling efforts to deliver on department and program objectives.
• CP representative for specific programs in Global Development Teams.
• Collaborate closely with related departments such as data management, biostatistics, clinical operations etc. to ensure full and effective integration of PK-related data within TOI activities.
• Collaboration with biomarker department and conduct PK/PD analysis (pharmacodynamic).
• Maintain collaboration with TPC (Taiho Pharmaceutical Japan) PK department.
• Manage a Team of talented individuals within CP department at TOI and provide supervision/mentorship as needed.

Education/Certification Requirements

• Advanced degree (Doctoral or Ph.D. is preferable) in pharmacology‑related discipline or quantitative sciences. If a candidate has a master’s degree, additional industry experience will be required.

Knowledge, Skills, and Abilities

• A minimum of 12 years of industry experience with focus on clinical development including oncology.
• Significant experience of PK, PK/PD, Modeling & Simulation including PopPK, ER and QSP analyses in clinical trials and the design and execution of CP and PK studies in oncology.
• Operational experience in CP/PK part of oncology clinical development.
• A working knowledge of the ICH/FDA/EU guidelines for CP/PK.
• Prior experience working in an interdisciplinary team.
• Excellence in written and oral communication.
• Demonstrated experience successfully managing a team and willingness to put the organization and team’s needs first.
• Experience with prior regulatory interactions, NDA/BLA submissions highly desirable.
• Deep working knowledge of drug development process.
• Ability to multi‑task.
• Attention to detail with a consistent focus on quality.
• Ability to read, analyze, and interpret professional journals and technical manuscripts.
• Ability to write reports, and procedures.
• Ability to effectively present information and respond to questions from internal and external clients.
• Ability to appropriately analyze CP/PK related data including pop‑PK analysis and modeling.
• Ability to define problems, collect data, establish facts, and draw valid conclusions.
• Ability to interpret abstract and concrete concepts.
• Experience using Data Management software, Windows and MS Office products specifically Word, Excel, PowerPoint, and WinNonlin.
• The employee is required to understand documents in English.

The pay range for this position at commencement of employment is expected to be between $263,500–$310,000 annually. This pay range is based on the market range for positions of this type. However, base pay offered may vary depending on multiple individualized factors, including market location, job‑related knowledge, skills, and experience. The total compensation package for this position may also include other elements, including annual bonus/incentive comp plans, potential long‑term incentive plan, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if a candidate/employee receives an offer of employment.

If hired, employee will be in an “at‑will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.

Equal Opportunity Employer Information: Taiho Oncology is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, gender, sex, age, religion, creed, national origin, ancestry, citizenship, marital status, sexual orientation, physical or mental disability, medical condition, veteran status, gender identity, genetic information, or any other characteristic protected by federal, state, or local law. Any applicant who, because of a disability, needs an accommodation or assistance in completing an application or at any time during the application process, please email [e-mail]. Taiho Oncology also provides reasonable accommodations to employees with disabilities consistent with our obligations under the law. Pursuant to applicable state and municipal Fair Chance Laws and Ordinances, we will consider for employment qualified applicants with arrest and conviction records.

The incumbent in this position may be required to perform other duties, as assigned.