- Genentech (Boston, MA)
- …need, including maximizing our pipeline assets targeting B-cells. The Senior Medical Director leads development of the Clinical Development (CD) strategy and ... participate in meetings, reviews, discussions and other interactions regarding early development studies to provide clinical science input and guidance; includes… more
- Genentech (Boston, MA)
- …Lead Medical Director makes major contributions to development of the Clinical Development (CD) strategy and plan and is responsible for effective and efficient ... in meetings, reviews, discussions and other interactions regarding early development/Phase I studies to provide clinical science input & guidance; including… more
- Veterans Affairs, Veterans Health Administration (Boston, MA)
- …its portfolio of local and national oncology and chronic disease research programs, clinical trials, and epidemiologic studies . MAVERIC is one of the largest ... cancer and chronic disease research program. Responsibilities This position serves as Director , Oncology and Chronic Disease Research at VA Boston Healthcare System.… more
- Sunrise Senior Living (Burlington, MA)
- …NAME** Sunrise of Burlington **Job ID** 2025-232029 **JOB OVERVIEW** The Resident Care Director (RCD) serves as the nursing clinical leader for the community ... health and wellness of the resident population. + Provide clinical care through the direct application of the nursing...services for the residents. + Serve as the CLIA Director as applicable for the community and according to… more
- Sumitomo Pharma (Boston, MA)
- … Protocols, Informed Consent Forms (ICF), Safety Management Plans (SMP), Clinical Study Reports (CSR), Investigator's Brochures (IB), Investigator communications ... Regulatory safety inquiries. + Represents PVRM on post-marketing product specific and/or clinical study team meetings and governance committees. + Performs… more
- Pfizer (Cambridge, MA)
- …and management of clinical protocols and amendments, investigator brochures, clinical study reports, statistical analysis plan, and regulatory documents. + ... Provide leadership to early stage clinical scientists on the clinical ...safety, pharmacology, and efficacy data from ongoing and completed studies for early development assets. + Oversee manuscripts, abstracts… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- **Associate Director , Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and drug ... relevant ICH and regulatory guidelines + Develop and implement stability study protocols and timelines, including sample collection, storage conditions, and… more
- Beth Israel Lahey Health (Burlington, MA)
- …a difference in people's lives.** Under the oversight of the Executive Director (with additional direction from the Division Chairs), the Administrative Director ... the annual budget and is responsible for the optimization of revenue cycle, clinical workflows, and provider productivity. This role serves as the principal liaison… more
- Grifols Shared Services North America, Inc (Fall River, MA)
- …more than 110 countries and regions. The primary responsibility of the MSL Field Director is the management, performance, and coaching of a team of MSL direct ... (MSL primary call points include Immunology, Neurology, Hematology/Oncology). The Field Director ensures compliant execution of field medical plans, strategy, and… more
- Sanofi Group (Cambridge, MA)
- …, medical, safety, and regulatory colleagues to provide labeling input relevant to clinical study protocols, especially in early and late development phases. + ... **Job Title:** Associate Director , Global Regulatory Affairs - Global Labeling Strategy...global labeling strategy for assigned products, including those in clinical development, life cycle management (LCM), and the marketed… more