Data Engineer - Senior Manager PwCData Engineer - Senior ManagerBoston, MA$124,000–$280,000 / yearCertification in Cloud Platforms [e.g., AWS Solutions Architect, AWS Data Engineer, Google Professional Cloud Architect, GCP Data Engineer Microsoft Azure Solutions Architect, Azure Data Engineer Associate, Snowflake Core, Snowflake Architect, Databricks Data Engineer Associate] is a plus. You also be responsible for developing and documenting data models, data flow diagrams, and data architecture guidelines, maintaining compliance with data governance and data security policies, and collaborating with business stakeholders to translate their data requirements into technical solutions.
Medical Laboratory Manager (CLS/MLS) MFM HealthMedical Laboratory Manager (CLS/MLS)Middleton, MAThe ideal candidate is a collaborative leader who enjoys mentoring staff, optimizing workflows, maintaining laboratory compliance, and working closely with providers and clinical teams to deliver accurate and timely diagnostic testing that supports exceptional patient care. Medical Laboratory Manager (CLS/MLS) Full-Time | MFM Health | Middleton, MAMFM Health is seeking an experienced and highly motivated Medical Laboratory Manager (CLS/MLS) to lead our laboratory operations at our Middleton, MA practice location.
Customer Success Manager, Workbench VerilyCustomer Success Manager, WorkbenchBoston, MassachusettsMust be accountable, possess a strong work ethic, a sense of urgency and ownership, and demonstrate the ability to work effectively both independently (delivering results under pressure, taking ownership) and collaboratively to achieve results without formal authority. Highly customer-centric, focused on driving outcomes and achieving objectives in partnership with the company, coupled with excellent interpersonal skills for efficient communication and collaboration across all internal and external levels.
Clinical Instructor, Diagnostic Radiography Brigham and Women's HospitalClinical Instructor, Diagnostic RadiographyBoston, MA$41.52–$56.59 / hourThe framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. In addition to competitive base pay, we offer comprehensive benefits, career advancement opportunities, differentials, premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth.
Associate Director, Clinical Operations Study Lead BlueRock Therapeutics LPAssociate Director, Clinical Operations Study LeadMassachusettsDrives operational initiatives key to successful study execution including but not limited to site identification/qualification, site activation strategy, site performance management, overall enrollment success (including mitigation/rescue actions as needed). Utilizing our proprietary CELL+GENE platform , we direct cellular differentiation and genetically engineer cells to create transformative therapies for patients suffering from neurological and ophthalmological diseases.
NewSocial Media & Content Manager StemWaveSocial Media & Content ManagerBoston, MassachusettsIf you don't have that yet: meaningful undergrad project work, coursework, or extracurricular involvement in content/social/marketing, with a portfolio or website you can point us to with real insights and creatives to show. StemWave manufactures and distributes premium medical technology to healthcare providers such as physical therapists, chiropractors, MDs, athletic trainers, and other private practice owners.
Lead Clinical Data Manager Integrated Resources, IncLead Clinical Data ManagerLexington, MassachusettsContractorTakes action to ensure study and project priorities are maintained; ensures adjustment of plans as priorities evolve Contributes to regular budget forecasting and regular cost accrual processes and proactively communicates to the team budgetary impacts of decisions or processes implemented to achieve results Courage to challenge. · Partnering with customers as a trusted consultant and becoming an integral part of customer's decision making Supports each clinical study and project team by ensuring data management plans and data handling activities are designed to meet project and protocol deadlines.
Lead Clinical Data Manager. Integrated Resources, IncLead Clinical Data Manager.Lexington, MassachusettsFull timeBuilding Authentic Relationships: Building trusting relationships that will enhance current and future needs Leads in developing trust through transparency in communication and individual actions; ensures outcomes are team driven rather than individually driven; promotes collaborative team and organizational success Key Skills, Abilities, and. Takes action to ensure study and project priorities are maintained; ensures adjustment of plans as priorities evolve Contributes to regular budget forecasting and regular cost accrual processes and proactively communicates to the team budgetary impacts of decisions or processes implemented to achieve results.
Sr. Clinical Study Manager Integrated Resources, IncSr. Clinical Study ManagerCambridge, MassachusettsFull timeProvides Clinical Operations input to other important study activities, including but not limited to: site identification and selection, enrollment models, clinical supply planning and drug supply, organization of investigator and vendor meetings, development of informed consents forms, planning and management of Trial Master File, development of monitoring plans, development of IxRS systems, development of EDC / Case Report Forms, review of data during the study, data cleaning and database lock, writing the Clinical Study Report. In collaboration with Study Execution Team (functions, Strategic Partners, and vendors), identify risks to study and suggest risk mitigation plans, with oversight of Clinical Program Manager and Associate Director, Clinical Operations to escalate risks and ensure rigorous risk mitigation planning.
Clinical Data Management Project Manager Integrated Resources, IncClinical Data Management Project ManagerCambridge, MassachusettsContractorMinimum of 5 years in the Data Management field, previous work with CROs and Data Management vendors is required, working in a global/cross-cultural setting is preferred In-depth knowledge and understanding of the drug development process and data management process. Technical/Software Skills: Familiarity with Oracle Clinical or other clinical data management system software; General software skills: Lotus Notes, MS Access, MS Word, MS Excel, MS Project Strong understanding of database programming concepts.
Hospice Staff RN/Case Manager 40 hour $5,000 Sign On Bonus Hebrew Rehabilitation CenterHospice Staff RN/Case Manager 40 hour $5,000 Sign On BonusDedham, MassachusettsRoutinely assesses patients’ response to plans of care and performs comprehensive assessments, hospice aide supervision, and coordination/oversight of hospice services provided in assisted living, LTC, SNF and hospital settings. Hospice will complete the continuum of outstanding care delivered by Hebrew SeniorLife, an integrated, eight-site system of health care, housing, research and teaching that serves thousands of seniors in the Greater Boston area and beyond and has been a nationally-recognized industry leader for over a century.
Hospice Staff Rn/Case Manager 40 Hour $5,000 Sign On Bonus Hebrew Senior LifeHospice Staff Rn/Case Manager 40 Hour $5,000 Sign On BonusDedham, MA$78,576.07–$117,864.10 / yearRoutinely assesses patients' response to plans of care and performs comprehensive assessments, hospice aide supervision, and coordination/oversight of hospice services provided in assisted living, LTC, SNF and hospital settings. Hospice will complete the continuum of outstanding care delivered by Hebrew SeniorLife, an integrated, eight-site system of health care, housing, research and teaching that serves thousands of seniors in the Greater Boston area and beyond and has been a nationally-recognized industry leader for over a century.
IT Infrastructure Manager VTal Technology Solutions LLCIT Infrastructure ManagerNewton, MAThe IT Infrastructure Manager is responsible for managing and maintaining the organization's enterprise IT infrastructure, including Windows environments, Microsoft 365, Intune, networking, cloud platforms, cybersecurity, and enterprise systems. Project & Vendor Management Plan, manage, and execute infrastructure projects including cloud migrations, Microsoft 365 implementations, Intune deployments, system upgrades, and network modernization initiatives.
Senior Contract Manager, Strategic Sourcing Brigham and Women's HospitalSenior Contract Manager, Strategic SourcingSomerville, MA$79,560–$115,720.80 / yearReporting directly to the Corporate Manager of Non-Clinical Strategic Sourcing in Supply Chain Management, the Senior Contract Manager will manage a large portfolio of contracts that range in size, scope, value and complexity. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success.
Clinical Project Manager III Integrated Resources, IncClinical Project Manager IIILexington, MassachusettsFull timeResponsibilities % of Time Job Function and Description 10 %: • Represents and leads the study team to design, develop and deliver the clinical study in accordance with the clinical development plan/strategy, budget and timeline • Authors/contributes to clinical study documents. Title: Clinical Project Manager III Location: Lexington, MA, United States Duration: 06+ Months Job Details: • Responsible for the planning, implementation, execution and management of one or more complex clinical research studies.
Clinical Safety Data Manager Integrated Resources, IncClinical Safety Data ManagerCambridge, MassachusettsFull timeThe AE Intake Clinical Trials Associate will provide partner / vendor oversight in relation to Clinical Trial safety report collection and will collaborate with other functions (e.g., Clinical Operations, Medical Affairs, Data Management, Medical Writing, Regulatory, Biostatistics, and others) to ensure consistency with regulations and with departmental goals and objectives. Acts as subject matter expert on Pharmacovigilance (PV) operations of Pre and Post-Marketing Clinical Studies during audits / inspections Senior Manager, Safety Data Collection, Clinical Trials 10%.
Clinical Trials Safety Data Manager Integrated Resources, IncClinical Trials Safety Data ManagerCambridge, MassachusettsContractorClinical Trials Associate will provide partner / vendor oversight in relation to Clinical Trial safety report collection and will collaborate with other functions (e.g., Clinical Operations, Medical Affairs, Data Management, Medical Writing, Regulatory, Biostatistics, and others) to ensure consistency with regulations and with departmental goals and objectives. Acts as subject matter expert on Pharmacovigilance (PV) operations of Pre and Post-Marketing Clinical Studies during audits / inspections Senior Manager, Safety Data Collection, Clinical Trials.
Clinical Data Manager Integrated Resources, IncClinical Data ManagerCambridge, MassachusettsContractorManage performance of vendors, in addition to, Data Managers and Senior Data Managers, for studies/programs run from the US, EU or Asia through the following: • Define program-level strategy for data management tasks and deliverables. • Directs the work of external vendors providing data capture technologies, data processing capabilities and data management programming capabilities to achieve quality, timely, cost-effective program/study deliverables.
Sr. Manager/Associate Director, Clinical Monitoring Oversight Aura Biosciences Inc.Sr. Manager/Associate Director, Clinical Monitoring OversightBoston, MA$150,000–$215,000 / yearThis role is responsible for the strategic oversight of Clinical Research Associates (CRAs) and/or monitoring vendors (CROs), driving site performance, data quality, patient safety, and inspection readiness across all regions in which the trial(s) are conducted. Minimum 7-10 years of clinical research experience, including significant on-site or remote monitoring experience (CRA/Senior CRA background strongly preferred); typically, 3+ years in a lead CRA, monitoring management, or comparable oversight role for AD-level.
Clinical Study Design Manager Science 37Clinical Study Design ManagerBoston, MAThe following qualifications are preferred and/or equivalent applicable experience: Required: 3+ years of experience in clinical research or life science industry, including at least 3 years in design of CRF/ePRO or other clinical trials database capture software. The Clinical Study Design Manager is responsible for working with our clients and internal staff to define the eSource platform specification design for the study, including all data capture requirements, bridging the gap between protocol requirements and implementation.