Jobs in All Categories (7) Science & Education (7)
Responsible for writing relevant sections in IND and other related regulatory documents.
Responsible for non-clinical pharmacokinetic/toxicokinetic and related ADME studies on small molecules to advance early and late stage programs.
The Senior Manager/Associate Director of Clinical Operations will work closely with team members and be responsible for the planning and execution of assigned clinical studies.
Solve problems on diverse topics from impurity identification to API polymorph control and engineering of physical properties.
The Scientist/Senior Scientist will performmethod development and validation, oversee analytical investigationsandstability programs, andconductprocess and product characterization.
Responsible for budget management of assigned projects, including vendor/site selection, budget negotiations, and approval of invoices; attend scientific meetings to stay current on new developments within relevant areas.
Transfer processes and methods to selected external vendors for cGMP drug product manufacture.