Associate Director, Quantitative Pharmacology, Clinical Pharmacology

Otsuka Pharmaceutical Companies (U.S.); Princeton (NJ); On-site; USD 169,000 - 253,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) match

Paid holidays

Tuition reimbursement

Job summary

Otsuka Pharmaceutical Companies (U.S.) in New Jersey is seeking a senior clinical pharmacology leader to drive PK/PD analyses, pharmacometrics, and regulatory submissions for IND/NDAs. You will partner with non-clinical, bioanalytical, formulation and early development teams to shape development strategies and pediatric plans.

The role requires advanced degree and 5+ years in clinical pharmacology with strong leadership, communication and cross-functional collaboration.

Qualifications

• In-depth knowledge of clinical pharmacology, PK/PD and bioanalytical chemistry.
• Experience in phase I operations, multi-region regulatory requirements, PK/PD analysis.
• Leadership in clinical pharmacology and strong communication skills.

Responsibilities

• Conduct PK and PK/PD analysis.
• Author regulatory submission sections including IND/NDA documentation.
• Lead pharmacometrics and modeling plans; provide input on modeling strategies.

Skills

Clinical pharmacology

PK/PD analysis

Biopharmaceutics

Bioanalytical chemistry

Leadership experience

Communication skills

Education

PhD/PharmD/MS in Clinical Pharmacology

Tools

Phoenix NLME

Job description

Job Summary

Supports all

Job Description

Job Summary

Supports all clinical pharmacology activities related to pre-IND, IND, phase1-3, PK, PK/PD and regulatory submissions. Supports study design, execution and reporting of clinical pharmacology and studies. Provides input into all phases of drug development including, but not limited to dose finding, dose optimization, exposure-response and pediatric development. Closely interacts with non-clinical and bioanalytical team members for design and execution of first-in-human, mass balance and drug interaction studies. Author of clinical pharmacology submission documents and representative of the department at different product development team meetings. participates in pharmacometrics and simulation and modeling plans and provide input on modeling and simulation activities. Interacts with early development and business development team members as well as external collaborators to assess/lead development and selection of pre-IND and early phase assets.

• Supports clinical pharmacology activities related to study design, protocol development, study execution, reporting and interpretation of data.
• Conduct PK and PK/PD analysis.
• Work closely with pharmacometrics team members and provides input related to analysis and reporting of PK and PK/PD.
• Authors development of clinical pharmacology sections for regulatory filings including annual reports, investigator’s brochure, IND/NDA applications and pediatrics development plans.
• Work with bioanalytical team members on activities related to assay development, sample management, pharmacogenomics and biomarker development.
• Work with formulation development groups and provide support for activities related to formulation development, dissolution testing, in vivo-in vitro correlations and biowaivers for pre- and post-approval formulations.
• Manage clinical pharmacology activities related to project budgets, outsourcing of PK and PK/PD analyses, contract requisition, SOW and approval of invoices.
• Training and mentoring of staff related to clinical pharmacology
• Serve as clinical pharmacology lead and pharmacometrics representative on multiple project teams and support model-based drug development strategies for ongoing projects.

Qualifications/ Required

Knowledge/ Experience and Skills:

Knowledge and Competencies

• In-depth knowledge of clinical pharmacology, PK, PD, drug metabolism, biopharmaceutics, and bioanalytical chemistry, Hands PK and PK/PD analysis and, Phoenix NLME, etc.
• Excellent working knowledge of phase I clinical operations, drug development, multi-region regulatory requirements and PK/PD analysis.
• Great working knowledge of formulation development, drug development and clinical development.
• Current awareness of the latest developments in clinical pharmacology, pharmacometrics and guidance documents.

Skills

• Must be able to apply scientific knowledge (in the areas specified above) to further the company’s products, anticipate and identify core problems, apply insightful analysis, and solve problems effectively.
• Strong leadership experience related to clinical pharmacology.
• Strong organization skills.
• Strong communication skills.
• Flexibility to react rapidly to changing situations/environment.

Travel 20%

Educational Qualifications

PhD, PharmD, MS in Clinical Pharmacology (or a related area such as pharmacokinetics, pharmacology, pharmaceutics) with a minimum of 5 years of experience in these areas. Experience in population PK and PK/PD modeling and statistical models a plus.

Competencies

Accountability for Results - Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change.

Strategic Thinking & Problem Solving - Make decisions considering the long-term impact to customers, patients, employees, and the business.

Patient & Customer Centricity - Maintain an ongoing focus on the needs of our customers and/or key stakeholders.

Impactful Communication - Communicate with logic, clarity, and respect. Influence at all levels to achieve the best results for Otsuka.

Respectful Collaboration - Seek and value others’ perspectives and strive for diverse partnerships to enhance work toward common goals.

Empowered Development - Play an active role in professional development as a business imperative.

Minimum $169,222.00 - Maximum $253,000.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States. Other elements may be used to determine actual pay such as the candidate’s job experience, specific skills, and comparison to internal incumbents currently in role. Typically, actual pay will be positioned within the established range, rather than at its minimum or maximum. This information is provided to applicants in accordance with states and local laws.

Application Deadline

This will be posted for a minimum of 5 business days.

Company benefits

Comprehensive medical, dental, vision, prescription drug coverage, company provided basic life, accidental death & dismemberment, short-term and long-term disability insurance, tuition reimbursement, student loan assistance, a generous 401(k) match, flexible time off, paid holidays, and paid leave programs as well as other company provided benefits.

Come discover more about Otsuka and our benefit offerings; https://ah-prod.com/multi/videoplayer/player.html?v=6385356920112.

Disclaimer

This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.

Otsuka is an equal opportunity employer. All qualified applicants are encouraged to apply and will be given consideration for employment without regard to race, color, sex, gender identity or gender expression, sexual orientation, age, disability, religion, national origin, veteran status, marital status, or any other legally protected characteristic.

If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation, if you are unable or limited in your ability to apply to this job opening as a result of your disability. You can request reasonable accommodations by contacting [e-mail].