Senior/Principal Pharmacokinetics Scientist

Freelance / Contract
USA
Posted 1 year ago
The job listing has expired. Unfortunately, the hiring company is no longer accepting new applications.

To see similar active jobs please follow this link: Remote Management jobs

ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative “one-team” culture. We are looking for a dynamic person to join our in-house team as a Senior/Principal Pharmacokinetics Scientist in the United States. The ideal candidate will possess a deep understanding of pharmacokinetics (PK) and pharmacodynamics (PD) theory and practice and will play a key role in the design, execution, and analysis of clinical pharmacology studies and other projects involving PK/PD. This position requires strong leadership in study concept development, protocol design, and the ability to work collaboratively with both internal teams and external clients.

Join our team: you can be part of making a difference in peoples' lives and experience a fulfilling and rewarding career!

Key Responsibilities:

  • Significant experience leading study concept and protocol design, authoring clinical pharmacology development plans, and creating modeling and simulation plans.

  • Conduct PK-PD, Pop PK-PD, and related analyses to support clinical trials, ensuring accurate data interpretation and integration into regulatory filings, clinical publications, and presentations.

  • Provide technical expertise and support in the use of standard PK and PD data analysis software, including Phoenix WinNonlin, NLME, R/R Studio, Monolix, NONMEM, and similar tools.

  • Collaborate closely with clients to understand project needs, provide expert guidance on clinical pharmacology, and deliver high-quality outcomes.

  • Prepare and review comprehensive PK/PD analysis reports, ensuring clear and precise communication of study results to clients and stakeholders.

  • Apply significant knowledge of pharmaceutical regulatory requirements related to clinical pharmacology to ensure compliance and support regulatory submissions.

  • Work effectively in cross-functional teams, including bioanalytical scientists, biostatisticians, and clinical operations, to ensure seamless project execution.

  • Provide mentorship and leadership to junior pharmacologists, contributing to the development and implementation of best practices within the team.

  • Stay current with advancements in clinical pharmacology, applying the latest knowledge to enhance project outcomes and client satisfaction.

Qualifications:

  • PhD in pharmaceutical sciences, pharmacology, life sciences, clinical pharmacology, pharmacokinetics, or a related discipline, with at least 3 years of relevant research or clinical experience in clinical pharmacology and pharmacokinetic-pharmacodynamic modeling within the pharmaceutical or biotechnology industry.

  • PharmD in a relevant discipline with a minimum of 5 years of experience in clinical pharmacology and PK/PD modeling and simulation.

  • Alternatively, a Master’s degree in a related field with at least 7 years of relevant experience in Clinical Pharmacology and Modeling & Simulation.

  • Robust knowledge of pharmacokinetics, pharmacodynamics, translational sciences, and PK/PD data analysis.

  • Hands-on experience and expertise with standard PK and PD data analysis software such as Phoenix WinNonlin, NLME, R/R Studio, Monolix, and NONMEM.

  • Strong communication and organizational skills, with the ability to present complex data to both scientific and non-scientific audiences.

  • Proven ability to manage multiple projects simultaneously and work effectively in a dynamic, client-oriented environment.

Preferred Qualifications:

  • Experience in working across a variety of therapeutic areas.

  • Prior experience working in a CRO setting is highly desirable.

  • Relevant certifications in clinical pharmacology or related disciplines are a plus.

#LI-TT1 #LI-Remote #Senior #Contract

 

About the Job
Freelance / Contract
USA
Posted 1 year ago
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Senior/Principal Pharmacokinetics Scientist

The job listing has expired. Unfortunately, the hiring company is no longer accepting new applications.

To see similar active jobs please follow this link: Remote Management jobs

ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative “one-team” culture. We are looking for a dynamic person to join our in-house team as a Senior/Principal Pharmacokinetics Scientist in the United States. The ideal candidate will possess a deep understanding of pharmacokinetics (PK) and pharmacodynamics (PD) theory and practice and will play a key role in the design, execution, and analysis of clinical pharmacology studies and other projects involving PK/PD. This position requires strong leadership in study concept development, protocol design, and the ability to work collaboratively with both internal teams and external clients.

Join our team: you can be part of making a difference in peoples' lives and experience a fulfilling and rewarding career!

Key Responsibilities:

  • Significant experience leading study concept and protocol design, authoring clinical pharmacology development plans, and creating modeling and simulation plans.

  • Conduct PK-PD, Pop PK-PD, and related analyses to support clinical trials, ensuring accurate data interpretation and integration into regulatory filings, clinical publications, and presentations.

  • Provide technical expertise and support in the use of standard PK and PD data analysis software, including Phoenix WinNonlin, NLME, R/R Studio, Monolix, NONMEM, and similar tools.

  • Collaborate closely with clients to understand project needs, provide expert guidance on clinical pharmacology, and deliver high-quality outcomes.

  • Prepare and review comprehensive PK/PD analysis reports, ensuring clear and precise communication of study results to clients and stakeholders.

  • Apply significant knowledge of pharmaceutical regulatory requirements related to clinical pharmacology to ensure compliance and support regulatory submissions.

  • Work effectively in cross-functional teams, including bioanalytical scientists, biostatisticians, and clinical operations, to ensure seamless project execution.

  • Provide mentorship and leadership to junior pharmacologists, contributing to the development and implementation of best practices within the team.

  • Stay current with advancements in clinical pharmacology, applying the latest knowledge to enhance project outcomes and client satisfaction.

Qualifications:

  • PhD in pharmaceutical sciences, pharmacology, life sciences, clinical pharmacology, pharmacokinetics, or a related discipline, with at least 3 years of relevant research or clinical experience in clinical pharmacology and pharmacokinetic-pharmacodynamic modeling within the pharmaceutical or biotechnology industry.

  • PharmD in a relevant discipline with a minimum of 5 years of experience in clinical pharmacology and PK/PD modeling and simulation.

  • Alternatively, a Master’s degree in a related field with at least 7 years of relevant experience in Clinical Pharmacology and Modeling & Simulation.

  • Robust knowledge of pharmacokinetics, pharmacodynamics, translational sciences, and PK/PD data analysis.

  • Hands-on experience and expertise with standard PK and PD data analysis software such as Phoenix WinNonlin, NLME, R/R Studio, Monolix, and NONMEM.

  • Strong communication and organizational skills, with the ability to present complex data to both scientific and non-scientific audiences.

  • Proven ability to manage multiple projects simultaneously and work effectively in a dynamic, client-oriented environment.

Preferred Qualifications:

  • Experience in working across a variety of therapeutic areas.

  • Prior experience working in a CRO setting is highly desirable.

  • Relevant certifications in clinical pharmacology or related disciplines are a plus.

#LI-TT1 #LI-Remote #Senior #Contract