- Parexel (Boston, MA)
- …for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies , in compliance with Client Procedural Documents, international ... **CRA and Sr CRA positions- Remote - Need for SE...escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance… more
- Parexel (Boston, MA)
- **Job Purpose:** The Senior Clinical Research Associate I ( Sr . CRA) is responsible for the site management, site monitoring and close-out of assigned ... Study Operations Manager (SOM) + When required Partners with other Study Team members (eg Clinician, Recruitment Specialist, Clinical Data Scientist) +… more
- Parexel (Boston, MA)
- The Senior Clinical Research Associate (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in ... for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies , in compliance with Client Procedural Documents, international… more
- ACROBiosystems Inc. (Boston, MA)
- …validation, candidate drug screening and optimization, CMC development, preclinical and clinical studies , commercial production, and companion diagnostics. We ... cross-functional collaboration and continuous learning. Job Summary The Regional Account Executive/ Manager (Junior to Senior level) role is responsible for… more
- Olympus Corporation of the Americas (Westborough, MA)
- … Affairs to execute clinical strategy activities and oversee aspects of clinical studies in support of clinical evidence generation strategies across ... of Olympus's portfolio. Specifically, this individual will be responsible for writing clinical study protocols, case report forms, and study … more
- Parexel (Boston, MA)
- …management activities **CSR Narratives (as applicable)** + Performing medical review of Clinical study report narratives according to the client's guidelines and ... and sign off adverse events report for accuracy and clinical importance, relationship to the study drug...processing cycle + Provide input as necessary to Feasibility Studies , Data Monitoring Committees (DMCs), Clinical Endpoint… more
- Parexel (Boston, MA)
- …of clinical trial samples + Provides support for sample related matters to clinical study teams + Works with Informed Consent Form (ICF) Specialist and ... Parexel FSP has an exciting opportunity for a Senior Precision Medicine Associate. This role works closely...trials. Performs other duties as necessary to ensure optimal clinical trial execution. **Key Accountabilities** **:** ** Study … more
- Novo Nordisk Inc. (Boston, MA)
- …products and services for their patients Maintain knowledge of the most recent clinical studies to inform customers and address questions, concerns, and ... CMCS I -Ecosystem I reports to the Ecosystem Business Manager . The CMCS I -Ecosystem I also must work...volume Utilize discretionary budget for maximum impact on sales Clinical Understanding Deep understanding of cardiometabolic disease state and… more
- Parexel (Boston, MA)
- …assigned project/ study . + Participate in the development and/or review of study documents, such as clinical protocols, Medical Monitoring Plans (MMP), ... Supporting Activities - Medical Support / Medical Monitoring for projects and studies contracted to Parexel - Deliver all medical support required for successful… more
- Actalent (Cambridge, MA)
- As a Senior Manager Clinical Study Lead... study team responsible for the delivery of clinical studies and research collaborations. You will ... study systems. Responsibilities + Lead the cross-functional study team for clinical study ...Ensure accurate budget management and address scope changes for studies . + Escalate issues related to study … more
