Dear All,
I wanted to reach out to you today to discuss a few new open positions with
some of our top clients. Below is a brief description of each role.
If interested please schedule a time to speak with our Recruiter, Elizabeth
Busch at https://meet.yesware.com/me/elizabeth13/30min.
*Principal Scientist Clinical Pharmacology*
*Key Responsibilities*
Support the clinical development and translational sciences programs.
Build pharmacostatistical models for population PK/PD and exposure-response
analyses.
Conduct meta-analysis and provide scientific input for dosage selection and
study designs.
Contributes to clinical pharmacology strategy and prepares modeling reports
for regulatory submissions.
*Job Requirements*
Ph.D. in Clinical Pharmacology, Pharmaceutical Sciences, or related field.
3+ years of industry experience.
Experience using modeling software such as NONMEM, R, Python, etc.
Experience analyzing data using modeling and simulation expertise.
*Principal/Senior Scientist Clinical Pharmacology*
*Key Responsibilities*
Lead the development of quantitative clinical pharmacology and modeling
strategies for cutting-edge therapies.
Apply advanced modeling approaches, such as PK/PD, PBPK, and quantitative
systems pharmacology to ensure safe and effective dosing.
Utilize model-based drug development principles for optimal drug
development.
*Job Requirements*
Ph.D. in Pharmacokinetics, Pharmaceutical Sciences, or related field.
5+ years' experience in clinical pharmacology and modeling & simulation
needed.
Must excel in quantitative clinical pharmacology and have a strong track
record in model-based drug development.
Responsibilities include leading clinical studies and engaging with global
health authorities.
*Senior Principal Scientist/Associate Director Clinical Pharmacology,
Modeling & Simulation*
*Key Responsibilities*
Responsible for conducting and overseeing clinical pharmacology studies and
analyses to support project decisions and regulatory requirements.
Lead the design and execution of phase I clinical studies and provide
dosing recommendations to project teams.
Contribute to regulatory documents and address queries from regulatory
agencies.
*Job Requirements*
Ph.D. in Clinical Pharmacology, Pharmaceutical Sciences, or related field.
7-10+ years of industry experience.
Experience in clinical pharmacology management and quantitative drug
development, including PK modeling.
Proficient in designing and reporting studies for regulatory submissions.