- Bristol Myers Squibb (Devens, MA)
- …+ Develop and manage a daily work plan for QC associates. Report out quality and operational metrics. + Responsible for management of QC samples and materials ... employee career development. + Oversee the training of the team members. + Review and approve procedures for Sample Management activities. + Collaborate with other… more
- Parexel (Boston, MA)
- …trial conduct. + Medical responsibility as co-author for the development of a robust Clinical Quality Monitoring Plan (CQMP) in line with the critical data, ... of the activity, related findings and resolutions. + Execution of relevant clinical quality monitoring for Study Physician using aggregated data outputs… more
- Humana (Boston, MA)
- …team and healthcare organization. The Medical Director's work includes computer based review of moderately complex to complex clinical scenarios, review ... and work is assisted by diverse resources which may include national clinical guidelines, CMS policies and determinations, Medicaid state contracts, clinical … more
- CenterWell (Boston, MA)
- …this knowledge in their daily work. The Medical Director's work includes computer-based review of moderately complex to complex clinical scenarios, review ... and work is assisted by diverse resources which may include national clinical guidelines, CMS policies and determinations, clinical reference materials, internal… more
- Regeneron Pharmaceuticals (Cambridge, MA)
- …in Clinical Trial Management (CTM). This individual is responsible for clinical operations activities and decisions including quality , timelines and budgets ... and proactively communicates progress, risks, issues or changes that may impact quality , timelines and/or budget; provide clinical program level updates to… more
- Actalent (Cambridge, MA)
- … Quality Management (RBQM) plays a critical cross-functional role in ensuring the quality and compliance of clinical trial execution by leading efforts across ... teams and CROs to align execution with risk and quality expectations throughout the clinical trial lifecycle....Lead and/or oversee centralized monitoring activities, including configuration and review of KRIs, QTLs, and data quality … more
- Bristol Myers Squibb (Cambridge, MA)
- …and rapid, data-driven decision making; and (iii) ensuring that only high quality and differentiated assets enter the market. Key Responsibilities Strategy and ... data-driven decision making on assigned projects. + Delivers high quality assets to commercial which have the potential for...Health Authorities and/or Advisory Committees in the design of clinical trials and endpoints. + Leads team to develop… more
- Humana (Boston, MA)
- …this knowledge in their daily work. The Medical Director's work includes computer-based review of moderately complex to complex clinical scenarios, review ... and work is assisted by diverse resources, which may include national clinical guidelines, CMS policies and determinations, clinical reference materials,… more
- Humana (Boston, MA)
- …this knowledge in their daily work. The Medical Director's work includes computer-based review of moderately complex to complex clinical scenarios, review ... and work is assisted by diverse resources, which may include national clinical guidelines, state policies, CMS policies and determinations, clinical reference… more
- EBSCO Information Services (Boston, MA)
- …writers, editors, and clinicians in your specialty area to create and further improve high- quality clinical content. **About You** + MD, DO or equivalent + ... than 2,700 people worldwide, with most embracing hybrid or remote work models. As an AI-enabled service leader, we...content created by an in-house editorial team, assessing for clinical relevance, accuracy, quality , and currency. This… more