Role
- Act as principal investigator and take full responsibility for assigned projects as well as supervision and training of the team
- Conduct preclinical and clinical pharmacokinetic (PK) non-compartmental analysis (NCA) independently using Pheonix WinNonlin®
- Analyze, and interpret preclinical and clinical PK studies (DMPK, ADME, BE/BA, TK, SAD, MAD, etc.) and data to optimize PK plan, sampling, and dosing
- Collaborate with 3rd Party CROs / consultants to prepare PK protocols, reports and supporting documents
- Support business development and marketing activities, foster client relationships and help onboard new clients
- Follow Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), and Study protocols
- Stay abreast of latest PK developments, regulatory guidance (FDA, ICH), and SOP benchmarks to improve the internal PK practices
Qualifications
- Ph.D. (2+ years) / M.S. (4+ years) in pharmacology, pharmacokinetics, pharmacometrics, biostatistics, or related areas
- Hands-on experience with pharmacokinetic (PK) studies, toxicokinetics (TK) studies, bioavailability & bioequivalence, biomarker testing, immunogenicity (ADA, NAb) testing
- Familiarity with bioanalysis using LC-MS/MS, ELISA, MSD, Luminex, Western Blot, and Thermofisher’s Watson LIMS is a huge plus
Benefits
- Competitive compensation
- Two weeks paid annual vacation
- 401k match and healthcare coverage to eligible employee
If interested, please e-mail your resume to careers@nebiolab.com.