- Catalent Pharma Solutions (Burlington, MA)
- ** Account Director , Biologics Drug Substance** Catalent Biologics is a fast-growing business within Catalent Pharma Solutions focused on providing ... facility in Madison, WI. This position has responsibility for establishing new biologics drug substance partnerships in the target territory. Success will… more
- Merck (Boston, MA)
- …molecules, biologics and non-traditional therapeutics like peptides, novel biological The Director is a skilled quantitative drug developer, with a strong, ... integrated understanding of the strategic elements of drug discovery and development. The Director should...of biopharmaceutical and ADME properties of small molecules and/or biologics Your role at our company is integral to… more
- Editas Medicine (Cambridge, MA)
- …agency briefing packages and response to regulatory authority queries. The Director will incorporate regulatory strategy and well positioned content into high ... execution of these submissions. Key Responsibilities: + As the Director , Regulatory CMC, you will be responsible for: +...delivery of all CMC regulatory milestones, including global investigational drug filings (eg, IND / CTA / IMPD /… more
- Merck (Boston, MA)
- …The Quantitative Pharmacology and Pharmacometrics (QP2) department drives model-informed drug discovery and development (MIDD) to routinely enable efficient ... drug discovery/development and/or regulatory decisions. The Pharmacometrics group within...company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas. This… more
- Merck (Boston, MA)
- …strategic elements of drug development. As a subject matter expert, the Director within the QP2-IO Group will work closely with teams of highly collaborative, ... and** **Pharmacometrics -** **Immune/Oncology** **(QP2-IO)** team in the role of Director . QP2-IO team is part of the Global Clinical Development organization… more
- Merck (Boston, MA)
- …for someone with a growth mindset. **Position Description:** The Senior Director , Global Regulatory Lead, is responsible for development and implementation of ... requirements for one or more company investigational and marketed drugs/ Biologics . Programs may be complex with more than one...but are not limited to:** + Reports to Executive Director or Associate Vice President, General Medicine + Develops… more
- Editas Medicine (Cambridge, MA)
- …tissues at least through IND, with more than one modality including biologics , small molecules, nucleic acid-based, or gene therapy products; and possess a ... timelines while maintaining high quality performance. Key Responsibilities: As the Senior Director , In Vivo Gene Editing Therapeutics, you will be responsible for: +… more