Principal Scientist, Nonclinical PK

  • Location

    United Kingdom
  • Salary

  • Job Type

  • Functions

    Scientific and Preclinical

About – This position will be responsible for ADME and PK studies for ADCs in an innovative and growing biotech.


  • Help design PK phase of non-GLP and GLP PK and toxicology studies for ADCs.
  • Be responsible for the toxicokinetics for non-GLP PK and toxicology studies, as well as all GLP toxicology studies.
  • Monitor studies from protocol development to data interpretation for CRO-based nonclinical ADME studies.
  • In charge of nonclinical PK sections of regulatory documentation, such as IND and BLA.
  • Present and provide PK data summaries for cross functional internal meetings.


  • PhD in Pharmacology (or other relevant subject area) followed by over 4 years in industry.
  • Extensive experience with small molecule ADME studies and PK/PD and TK modelling.
  • Experience with ADCs is highly desirable.
  • Proficiency in relevant computer systems for PK/PD studies.
  • Previous experience writing the nonclinical PK sections of regulatory documentation.
  • Excellent communication, both verbal and written.

Why apply?

The role is a great opportunity to join a growing biotech and make a difference as part of a committed team developing ADC therapies for cancer patients.

Please submit your CV to us for a private and confidential discussion about the opportunity.

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