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The impact you will make:Agios Pharmaceuticals is searching for a dynamic MSL/Sr. MSL (Medical Science Liaison) to join our growing Medical Affairs team. The MSL will conduct scientific exchange with KOLs in supporting Global Medical Affairs goals and objectives.
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Must have the ability to communicate positively to all LOL, customer, regulatory or vendor representatives as needed. Lead will work closely with the Maintenance Supervisor/Manager, Maintenance Planner/Scheduler, Mechanics and key production personnel.
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Capital One is hiring a technical Cyber Security professional to join the Data Loss Prevention (DLP) team and work with the line of business stakeholders building DLP system policies/ruleset based on ongoing regulatory requirements and analysis of user business processes and workflows.
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Maintain required documentation according to DDS, DMH, MassHealth, HUD, DPH, CARF, and all applicable regulatory standards as well as Bridgewell policies and procedures. Provide services to individuals according to DDS, DMH, MassHealth, HUD, DPH, CARF, and all applicable regulatory standards, as well as Bridgewell policies and procedures.
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Initiate and lead the development of a cross-portfolio external engagement strategy and related tactics for prioritized external organizations and HCPs, aligned across Global Medical Affairs Oncology, Commercial, Patient Value, Policy & Access, R&D, Corporate Communications & Advocacy, Health Equity and Patient Affairs, and with other key cross-functional/ex-Oncology partners as needed to ensure a one company approach to external engagement strategy, objectives, and execution.
$80 - $97.35 an hourFull-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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The Cyber Information Assurance Specialist will define requirements for business continuity, operations security, cryptography, forensics, regulatory compliance, internal counterespionage (insider threat detection and mitigation), and physical security analysis (including facilities analysis and security management) to best protect company assets.
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Minimum of 10 years of experience in site assessment and restoration working under the provisions of the MCP (Massachusetts Contingency Program) or other state regulatory programs, CERCLA and RCRA with experience managing HTRW type Federal projects.
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Understands and adheres to all Bank Secrecy Act and Anti-Money Laundering (BSA/AML), regulatory, security, retail banking and bank-wide policies and procedures. Understands and adheres to all Bank Secrecy Act and Anti-Money Laundering (BSA/AML), regulatory, security, retail banking and bank-wide policies and procedures.
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Lead cGMP manufacturing of TScan cell therapy products while adhering to cGMPs, SOPs, compliance/regulatory mandates, safety procedures, and quality requirements. TScan's discovery platform is centered around a breakthrough technology that enables the rapid, comprehensive, and genome-wide identification of the peptide antigen targets of T cell receptors.
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Collaborate with regulatory affairs teams to establish robust authoring, review and content strategy practices. Extensive experience with regulations and requirements such as cGMP, ICH, USP, JP and global CMC regulatory expectations and proven track-record of resolving complex issues with health authorities.
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The MDMP interacts and partners with marketed products R&D function leads (regulatory affairs, pharmacovigilance, global development operations and project management) to set R&D strategy and prioritize R&D functional support for assigned MP portfolio.
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As Section Lead/Sr. Project Manager, this position will manage our Massachusetts-based technical team servicing the commercial, industrial, private, and federal sectors nationwide and will work with a wide variety of clients, from local manufacturers to complex high-visibility Brownfield redevelopment projects and Federal HTRW projects working under provisions of CERCLA and RCRA.
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Exciting opportunity to be a driving force in making RI an industry-leading organization through improved customer experience, operational excellence, and proactive regulatory compliance for Class I and II Picture Archiving and Communication Systems (PACS) related medical devices, as well as non-medical devices.
$128,000 - $236,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Data Management and ReportingMaintains accuracy of ER event data and Leadership Society donor information in Harvard’s Alumni Affairs & Development database (Advance); reviews monthly data related to fundraising and engagement goals for Leadership Society and maintains donor lists and documentation in Advance.
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Adheres to regulatory requirements, e.g., DPH, TJC, DMH, Medicare, etc. There are 18 beds available on this inpatient unit of which we see various types of psychiatric illnesses such as Schizophrenia bi-polar and affective disorders, Personality disorders, Duel diagnosis, Adjustment disorder, Psychosis, and use DBT/CBT Group Therapy.
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regulatory affairs jobs Title: sr regulatory affairs associate in Lexington, MA
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