Join the team at Medivation [www.medivation.com] for an exciting opportunity to
take molecules from bench to bedside! In this role, you will evaluate the
preclinical and clinical PK, PK/PD, and metabolism properties of small molecule
drug candidates. You will collaborate with colleagues in Clinical,
Preclinical, Chemistry, Regulatory, and CMC in a team-oriented environment to
support programs in all phases of development. You will be responsible for
preclinical DMPK studies, preclinical PK/TK analyses, and clinical pharmacology
studies, including first-in-human studies. You will prepare nonclinical,
biopharmaceutical, and clinical pharmacology sections for regulatory
submissions. For consideration, submit your CV to Human Resources
([email protected]).
Experience:
· Position requires PhD and minimum of ten years of related experience
in Biotech/Pharmaceutical industry.
· Experience must include leadership role in the design and management
of human studies, authorship of relevant IND and NDA sections, and company
representation at FDA meetings.
· Hands-on experience with PK/PD modeling and simulation is required;
population PK modeling is a plus.
Joyce Mordenti, PhD | Vice President, Translational Medicine and DMPK
| Medivation, Inc., 201 Spear St., Third Floor, San Francisco, CA 94105
(P: 415.829.4125 | F: 415.543.3411 | * [email protected] |
http://www.medivation.com