Scientist II, Discovery DMPK
Listed on 2026-09-12
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Research/Development
Pharmaceutical Science/ Research, Research Scientist, Clinical Research, Drug Discovery
About Pharmaron
Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services.
Position:
Scientist II, Discovery DMPK
Location:
Exton, PA (onsite)
Salary Range: $55,000-$65,000
About PharmaronPharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services. We're proud of the impact we make and just last year, we supported over 780 discovery projects, 1,000+ CMC programs, and 1,000+ clinical trials across all phases.
Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,000 global customers. To learn more, visit
Are you passionate about advancing drug discovery through innovative bioanalytical science? We're seeking a Scientist I/II to join our growing Discovery DMPK team. In this role, you'll contribute to critical in vivo pharmacokinetic (PK) and in vitro ADME studies, supporting pharmaceutical and biotechnology clients as they develop the next generation of therapeutics. This is an excellent opportunity for an analytical scientist with LC-MS/MS expertise who enjoys working in a collaborative, fast-paced contract research environment where scientific excellence and client service go hand in hand.
Key Responsibilities- Design scientifically sound studies that support sponsor and internal research objectives.
- Perform sample analysis for Discovery DMPK studies, including in vivo PK and in vitro ADME programs.
- Execute and optimize LC-MS/MS assays following established development guidelines.
- Review and execute study protocols while ensuring data integrity and scientific quality.
- Author protocols, technical reports, and study summaries.
- Process, analyze, interpret, and review scientific data.
- Troubleshoot analytical methods and resolve technical challenges.
- Collaborate with scientists, project managers, laboratory personnel, vendors, and commercial teams to ensure successful project execution.
- Serve as a Principal Investigator (PI) or Study Director (SD) within areas of expertise, as appropriate.
- Bachelor's degree in Pharmacokinetics, Chemistry, Biochemistry, or a related scientific discipline.
- Minimum 2 years of laboratory experience within a CRO, biotechnology, or pharmaceutical environment.
- Minimum 2 years of hands-on LC-MS/MS (Mass Spectrometry) experience.
- Experience supporting bioanalysis across diverse molecule types.
- Knowledge of in vivo pharmacokinetic studies.
- Strong scientific writing, communication, organizational, and analytical skills.
- Ability to manage multiple priorities while maintaining exceptional quality and attention to detail.
- Detail-oriented with exceptional scientific integrity.
- Self-motivated and adaptable in a collaborative environment.
- Comfortable working independently while contributing to cross-functional teams.
- Committed to quality, compliance, and continuous improvement.
- Full-time, 100% on-site laboratory position.
- Work in both laboratory and office settings.
- Ability to stand or sit for extended periods.
- Lift up to 15 pounds as needed.
- Use standard laboratory equipment while wearing required personal protective equipment (PPE), including laboratory coats, gloves, and safety eyewear.
Pharmaron…
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