- Merck (Boston, MA)
- **Job Description** The Director / Principal Scientist , Regulatory Affairs Liaison, is responsible for the development and implementation of worldwide ... regulatory strategy for their assigned projects in the General...external to GRACS. **Key functions:** + Reports to Senior Principal Scientist (Senior Director ) and/or… more
- Merck (Boston, MA)
- **Job Description** In this Sr. Principal Scientist / Director position within Translational Oncology, this team member will provide leadership for aligned and ... Teams (ADTs) and our diagnostic partners. Position reports to Executive Director , CDx. **Primary Responsibilities** : + Direct CDx/IVD development projects,… more
- Bristol Myers Squibb (Cambridge, MA)
- …oncology. + Manage relationships with key internal stakeholders including regulatory , clinical and commercial and scientific communications and external ... human genetics, immunology). + Minimum of 6 years post-PhD experience for Sr. Principal Level (and minimum of 8 years Post-PhD experience for AD Level), with… more
- Merck (Boston, MA)
- **Job Description** The Senior Director (Senior Principal Scientist ) has primary responsibility for the planning and directing clinical research activities ... cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Senior Director … more
- AbbVie (Cambridge, MA)
- …more than 170 countries. Analytical Research and Development is seeking a Director (oral) Peptides to conduct process research and formulation development of ... drug substance and drug product development. + Experience developing global regulatory strategies including authoring regulatory submissions, and responding to… more
- Merck (Boston, MA)
- **Job Description** The Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director… more
- Bristol Myers Squibb (Cambridge, MA)
- …acting on Clinical Trial data to support development, and + Serving as principal functional author for Regulatory submission, study reports, and publications + ... at work and in their personal lives. Read more: careers.bms.com/working-with-us . ** Director , Early Clinical Development (MD) - Hematology & Cell Therapy with Focus… more
- Bristol Myers Squibb (Cambridge, MA)
- …and acting on clinical trial data to support development + Serving as principal functional author for Regulatory submission, study reports, and publications + ... their personal lives. Read more: careers.bms.com/working-with-us . **Job Title** Director , Early Clinical Development - Immunology **Functional Area Description**… more