In vitro ADME Senior/Principal Scientist – DMPK
Location: Exton, PA
Department: DMPK (Drug Metabolism & Pharmacokinetics)
Employment Type: Full-Time
Company
Frontage Laboratories Inc. is an award winning, publicly listed, full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada, and China, growing significant YoY growth. Our core competencies include pre-clinical, drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.
Position Summary
Frontage Laboratories is seeking an experienced and highly motivated Senior/Principal Scientist to join our In Vitro ADME group. This is a laboratory-based position responsible for the development, execution, interpretation, and reporting of a broad range of in vitro ADME studies supporting drug discovery and IND-enabling programs.
Roles & Responsibilities
- Design, perform, troubleshoot, and interpret a broad range of in vitro ADME studies including metabolic stability, CYP inhibition, time-dependent inhibition (TDI), CYP induction, reaction phenotyping, enzyme kinetics, plasma protein binding, blood-to-plasma partitioning, tissue binding, using LC-MS/MS-based analytical methods.
- Independently conduct routine and complex ADME assays while ensuring high-quality data generation and timely project completion.
- Perform sample preparation, LC-MS/MS analysis, data processing, and result interpretation.
- Prepare study protocols, technical reports, and scientific summaries.
- Troubleshoot experimental and analytical challenges and implement appropriate solutions.
- Maintain laboratory instruments and ensure compliance with SOPs, quality standards, and laboratory safety requirements.
- Support client discussions by providing scientific expertise in study design and data interpretation.
Education & Requirements
- Ph.D. or MS degree in Pharmaceutical Sciences, Analytical Chemistry, Biochemistry, Pharmacology, or related discipline with more than 5 years of relevant industry experience,
- Strong hands-on experience with multiple in vitro ADME assays.
- Extensive experience with LC-MS/MS-based quantitative bioanalysis is preferred.
- Strong troubleshooting and laboratory problem-solving skills.
- Good written and verbal communication skills.
- Ability to manage multiple studies in a fast-paced CRO environment.
Salary and Benefits:
Frontage Laboratories offers a competitive compensation and generous benefits package including health and dental insurance, a 401(k) plan, health insurance, short and long-term disability insurance, life insurance etc.
Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.
Skills Required
- Ph.D. or MS degree in Pharmaceutical Sciences, Analytical Chemistry, Biochemistry, Pharmacology, or related discipline with more than 5 years of relevant industry experience
- Strong hands-on experience with multiple in vitro ADME assays (metabolic stability, CYP inhibition, TDI, CYP induction, reaction phenotyping, enzyme kinetics, plasma protein binding, blood-to-plasma partitioning)
- Extensive experience with LC-MS/MS-based quantitative bioanalysis
- Strong troubleshooting and laboratory problem-solving skills
- Good written and verbal communication skills
- Ability to manage multiple studies in a fast-paced CRO environment
What We Do
Frontage Laboratories, Inc. is a CRO that provides integrated, science-driven, product development services throughout the drug discovery and development process to enable pharmaceutical and biotechnology companies to achieve their development goals. Comprehensive services include drug metabolism and pharmacokinetics, analytical testing and formulation development, preclinical and clinical trial material manufacturing, bioanalysis, preclinical safety and toxicology assessment and early phase clinical studies. Frontage has enabled many biotechnology companies and leading pharmaceutical companies of varying sizes to advance a myriad of molecules through development and file regulatory submissions in the United States, China and other countries.
