Principal Scientist, Nonclinical PK

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

Duties

• 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.

Experience

• 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.