Job Description
Primary purpose and function of this position:
Nonclinical DMPK Project Leader is responsible for nonclinical PK/ADME related programs and activities in frame of nonclinical DMPK department. For performance of PK and ADME studies for Global R&D projects and support of nonclinical and clinical PK/ADME and bioanalytical activities, as requested.
Major duties and responsibilities:
Plan, design, and lead non-clinical ADME and PK drug development plans, as well as bioanalytical plans, for projects in Global R&D in close collaboration with other departments.
Initiate, coordinate and lead the performance of bioanalytical, ADME, PK and PKPD, PBPK modeling activities in according to updated program and specific needs of individual project at CRO and in-house.
Calculates, analyze and predict PK properties and implications of innovative as well as generic drugs: low molecular weight and biologics.
Write DMPK sections of regulatory documents and company presentations
Support nonclinical toxicology and pharmacology drug development programs, as well as clinical pharmacology.
Report to relevant forums and managers on all above mentioned
Qualifications
Ph.D. in Life Science
Knowledge in pharmacokinetics
Experience in drug research and development
Good communication skills
Good spoken and excellent writing English
Excellent ability to work as a part of a team as well as independently
Creative mindset along with analytical skills
Experience in bioinformatics, knowledge in bioanalysis and experience in modeling- advantage
https://careers.teva/job/Netanya-1111/741299800/?locale=en_US