Drug Development Jobs
JGB BioPharma Consulting Inc. - , CA, United States
4+ years of experience with small-molecule drug synthesis and demonstrated skill in synthetic route optimization Experience in linker...
from: linkedin.com - 4 days ago
Exemplify Biopharma, Inc., a Symeres Company - , NJ, United States
Chemistry, Manufacturing and Controls (CMC) throughout the drug development and regulatory market application processes. Using a unique combination of program management, coupled with our New Jersey based R&D
from: linkedin.com - 5 days ago
Meet - , CA, United States
Meet’s innovative and fast-growing client has engaged us on an exciting new search for a talented Senior Scientist of Drug Product. You will be responsible for leading formulation development across
from: linkedin.com - 11 days ago
US Tech Solutions - , MD, United States
in early and late development • Proven track record of regulatory drug development including product approval/launch. • Experience in leading Major Health Authority interactions • Ability to think
from: linkedin.com - 11 days ago
SciPro - , CA, United States
An exciting SF-based biotech is hiring for a Senior Director of Drug Product Development (Late-Stage). In this role, you will have the opportunity to: - Lead formulation development strategy
from: linkedin.com - 10 days ago
Neurocentria, Inc. - Walnut Creek, CA, United States
The CMC Director of Drug Substance Development and Manufacturing is primarily responsible for the development and manufacturing of small molecule drug substances in support of clinical development
from: linkedin.com - 13 days ago
Proclinical Staffing - San Francisco, TX, United States (+9 locations)
clinical studies Sound knowledge of drug development and understanding of FDA and ICH GCP guidelines Proven problem solving and project management skills Excellent verbal and written communications skills
from: linkedin.com - 4 days ago
Corbus Pharmaceuticals - , MA, United States
proficiency in knowledge of the disease area(s), KOLs, indication(s), compound(s) under study (including MOA, PK/PD, biomarker & safety profile) A thorough understanding of the drug development process from pre
from: linkedin.com - 4 days ago
GQR - , CA, United States
knowledge of ICH, FDA, and EU GMP and GLP regulations with all phases of drug development. All onsite employees and contractors to be fully vaccinated prior to their first day.
from: linkedin.com - 4 days ago
Abilita Therapeutics, Inc. - , CA, United States
. Their mission is to unlock the therapeutic potential of membrane protein targets considered 'intractable' or 'undruggable,' by overcoming limitations that have hindered drug development in this area
from: linkedin.com - 4 days ago
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