- Bristol Myers Squibb (Cambridge, MA)
- …Operations and Procurement. + Determines appropriate assays and vendors for clinical biomarkers, and manages outsourcing of biomarker assay development ... and be responsible for setting strategy for translational activities including clinical biomarker activities to support drug development programs. This individual… more
- Takeda Pharmaceuticals (Boston, MA)
- …actions, and driving process standardization and change management activities. + Work with Clinical Partner Outsourcing (CPO) team to ensure execution of studies ... experience, global experience preferred. + Experienced and knowledgeable across key clinical operational functions (eg project management, clinical monitoring,… more
- Regeneron Pharmaceuticals (Cambridge, MA)
- …System (CTMS), Trial Master File (TMF) etc. + Ensures compliance with the clinical trial registry requirements + Identifies outsourcing needs of the study ... MA office. Fully remote is not eligible._ The **Senior Clinical Study Lead** (CSL) is expected to operate with...for the global execution of assigned large and/or complex clinical trials from study design, through execution, to study… more
- Takeda Pharmaceuticals (Boston, MA)
- …to support project goals. + This individual will contribute to the clinical pharmacology and pharmacometrics strategy to support PDT project progression from entry ... to clinical development to life cycle management + This individual...as well as relevant sections of CSRs. + Manage outsourcing activities and approved budget accordingly. Manage contract requisition,… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- **Job Summary** Under the direction of the Director/Associate Director of Clinical Management, the Senior Clinical Study Manager is responsible for the oversight ... and management of Otsuka clinical studies, including coordination with other relevant parties (eg, other Otsuka departments, external service providers (ESPs),… more
- Takeda Pharmaceuticals (Boston, MA)
- …of my knowledge. **Job Description** **About the role:** The Associate Director, Clinical and Safety Quality Compliance is responsible for ensuring the quality of ... process in partnership with functional compliance teams for regulations impacting Clinical , Safety and Clinical Pharmacovigilance Medical Quality (CPMQ)… more
- Takeda Pharmaceuticals (Boston, MA)
- …of my knowledge. **Job Description** **About the role:** Associate Director, Clinical Program Quality Investigations is responsible for ensuring the compliance of ... supports Takeda's mission by maintaining high standards of quality and compliance in clinical trials. **How will you contribute:** + Drive the implementation of … more
- Takeda Pharmaceuticals (Cambridge, MA)
- …community. You will have experience leading or supporting the procurement, sourcing, outsourcing , purchasing or buying of compliance or clinical supplier ... the best of my knowledge. **Job Description** **Global Category Manager- Clinical Development Services Procurement** **Cambridge, MA** **Hybrid** **Job Posting… more
- Takeda Pharmaceuticals (Boston, MA)
- …my knowledge. **Job Description** **R0150513 Global Category Manager - Clinical Development Services Procurement** **OBJECTIVES:** **The Global Category Manager ... (GCM) - Clinical Development Services Procurement at the Associate Director level,...community.** You will have experience leading the procurement, sourcing, outsourcing , purchasing or buying of Compliance Services categories, including… more
- Takeda Pharmaceuticals (Boston, MA)
- …to an effective partnership between Takeda study teams, study sites and the Clinical Research Organization (CRO) (ie, the Clinical Research Associate (CRA)). The ... study recruitment strategies, and mitigates barriers at the direction of Clinical Programs. + The Associate Director, Study Site Engagement supports Takeda… more
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