Protagonist Therapeutics, Inc.

Senior Director/Executive Director, Clinical Pharmacology

Protagonist Therapeutics, Inc.$275K — $310K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Advanced degree (PhD, MD, PharmD) in pharmaceutical or pharmacology-related discipline
  • Minimum of 10 years in clinical development or quantitative sciences
  • Extensive experience in clinical pharmacology including PK/PD and trial analysis
  • Proven record in developing clinical pharmacology programs for early and late-stage development
  • Strong ability to manage multiple priorities in a fast-paced environment
  • Published scientific work and experience in regulatory interactions
  • Knowledge of regulatory guidance related to clinical pharmacology

Responsibilities

  • Lead the development and execution of clinical pharmacology and pharmacometrics activities
  • Provide strategic leadership for population PK/PD modeling and dose selection
  • Collaborate with cross-functional teams to implement clinical pharmacology plans
  • Guide the progression of drug development candidates through clinical stages
  • Execute quantitative plans for clinical pipeline projects
  • Contribute to regulatory submissions for clinical studies
  • Mentor and develop junior clinical pharmacology scientists

Benefits

  • 100% coverage of medical, dental, and vision premiums for employees and dependents
  • Flexible Spending Accounts for healthcare and dependent care
  • 401(k) plan available
  • Flexible vacation policy
  • Comprehensive life insurance options
  • Short and long-term disability coverage
  • Company-paid lunch and snacks
Full Job Description
Senior Director/Executive Director, Clinical Pharmacology

Position Summary

Protagonist Therapeutics, Inc is seeking an experienced professional to join the Clinical Pharmacology and Pharmacometrics department. The candidate will lead and execute clinical pharmacology and pharmacometrics efforts for a portfolio of clinical studies, spanning first-in-human through late-stage development. Working in close partnership with cross-functional partners, the candidate will develop and execute clinical pharmacology plans and serve as a functional representative on development teams and regulatory interactions. The candidate will contribute to and conduct PK/PD and quantitative analyses and interpretation of clinical pharmacology studies.

We are committed to a thriving in-office culture. This role requires being on-site at our office in Newark, CA 4 days a week.

Responsibilities
  • Lead the development and execution of integrated clinical pharmacology, pharmacometrics and model-informed drug development activities across all stages of development
  • Provide scientific and strategic leadership and execute population PK, PK/PD, exposure-response, and PBPK modeling to support dose selection, study design, regulatory interactions, and key development decisions
  • Work in partnership with members of cross-functional teams to lead, develop and execute clinical pharmacology plans
  • Provide scientific and operational leadership to progress development candidates from discovery through late-stage clinical development
  • Develop and execute quantitative plans to support clinical development of pipeline projects
  • Contribute to regulatory submissions
  • Mentor and develop clinical pharmacology scientists, fostering scientific excellence, collaboration, and professional growth within the department.


Required Skills & Qualifications
  • Advanced degree (PhD, MD, PharmD) in pharmaceutical or pharmacology-related discipline or quantitative sciences
  • A minimum of 10 years of industry experience with focus on clinical development or application of quantitative sciences
  • Significant experience with clinical pharmacology, including PK/PD, quantitative sciences, biomarkers and analyses of clinical trials
  • Demonstrated experience developing and executing clinical pharmacology programs supporting first-in-human and clinical development programs
  • Demonstrated ability to manage multiple priorities and be productive and successful working cross-functionally in a fast-paced, matrixed organization
  • Strong scientific background, demonstrated through peer-reviewed publications, regulatory interactions, and presentations.
  • Working knowledge of regulatory guidance related to clinical pharmacology and pharmacokinetics
  • Excellent written and oral communication, including ability to convey complex concepts, with the ability to build strong working relationships with colleagues, cross-functional teams, and external partners
  • Attention to detail with a consistent focus on quality
  • Ability to effectively present information to stakeholders

Pay Range

The base pay range for this position at commencement of employment is expected to be between $275,000 and $310,000/year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience.

Benefits

A top priority for Protagonist Therapeutics, Inc. is to provide a robust and comprehensive health and wellness program for our employees and their families. We offer a variety of high-quality coverage and benefit options.
  • Health Care benefits. Protagonist covers 100% of the premium cost for medical, dental, and vision coverage for all full-time employees and their dependents.
  • Flexible Spending Accounts - Healthcare FSA, Dependent Care FSA, Commuter Benefits
  • 401(k) Plan
  • Flexible Vacation Policy
  • Life Insurance (Basic, Voluntary & AD&D)
  • Short Term & Long Term Disability
  • Company paid lunch and snacks

About Protagonist Therapeutics, Inc.

Protagonist Therapeutics, Inc. is a clinical-stage biopharmaceutical company that discovers and develops peptide-based therapeutics to address significant unmet medical needs. The company's pipeline includes PTG-300, an injectable hepcidin mimetic for the treatment of iron overload-related rare diseases, including beta-thalassemia and polycythemia vera; and PN-943, an oral, gut-restricted alpha-4-beta-7 integrin antagonist peptide for the treatment of inflammatory bowel disease. Protagonist Therapeutics, Inc. was founded in 2006 and is headquartered in Newark, California.
Learn more about Protagonist Therapeutics, Inc.
Size
122 employees
Market Cap
$483 million
Industry
Net Income
-$66.1 million
Founded
2001
Revenue
$28.6 million
NASDAQ

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