NewClinical Specialist, Enabling Technologies (Manchester, NH) StrykerClinical Specialist, Enabling Technologies (Manchester, NH)Manchester, New HampshireRemoteHowever, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. Provide surgeons and operating room staff with training and Clinical/Technical support in the operation of the company's navigation technologies, associated equipment and instruments to insure procedural efficiency.
Clinical Director - Juvenile Justice Eliot Community Human ServicesClinical Director - Juvenile JusticeBrockton, MAThis highly structured, self-contained program provides comprehensive interventions for juvenile offenders, including fully accredited schools and clinical support with individual and group therapy, staffed by trained professionals. We foster belonging in the workplace by identifying and removing barriers that may prevent individuals of all backgrounds from reaching their full potential, advancing into leadership roles, and fully engaging at all levels of the organization.
medical writer Integrated Resources, Incmedical writerCambridge, MassachusettsContractorResponsibilities include serving as the point contact interacting with the medical writing vendor, coordinating pertinent work streams, and overseeing outsourced SRLs/FAQs development processes; drafting and/or oversight of the development of Medical Information SRLs for assigned products; coordination of Content Development work-streams within or outside of Global Medical; providing internal Medical Information quality reviews of SRLs as needed; maintenance of SRLs within the database. Includes researching scientific literature and internal research documents and data feeding the vendor; tracking SRLs/FAQs development status in Veeva; documenting and reporting KPI metrics; facilitating review and approval processes.
Clinical Research Associate CTTX HealthClinical Research AssociateCambridge, MAWe’re looking for a Clinical Research Associate (CRA) to join a fast-growing biotech company (confidential) that’s advancing innovative therapies in neuroscience. Collaborate with site staff and cross-functional teams to solve challenges and keep trials on track.
NewDirector, Financial Reporting Formation BioDirector, Financial ReportingBoston, MA$185,500–$232,000 / yearDemonstrated ability to convert complex accounting guidance into practical calculations, journal entries, disclosures and repeatable processes, with experience including the following: consolidations (including experience with VIEs), noncontrolling interests and other ASC 810 issues, financial instruments, liability and equity accounting, share-based compensation, revenue recognition, ASC 820 fair value, licensing and collaboration arrangements, leases, capitalized software and R&D related accounting, Experience in Consolidation of a complex organizational structure. The Director is responsible for GAAP compliant ASC 810 consolidation, prepares the financial statements and footnotes, converts technical accounting conclusions into calculations, entries, workpapers and repeatable processes, manages the day-to-day flow of the external audit, and supports the reporting and audit of the company's separately audited venture fund.
Senior Manager/Associate Director, Business Systems (Coupa, Netsuite, etc) Kura OncologySenior Manager/Associate Director, Business Systems (Coupa, Netsuite, etc)Boston, MA$160,000–$186,000 / yearThe Senior Manager/Associate Director, Business Systems serves as the lead to Kura's business platforms including but not limited to Finance, Procurement and Contracting applications, with primary ownership of the system operations, workflows, financial controls and related integrations, and future enterprise applications. Kura developed and is commercializing KOMZIFTI® (ziftomenib), the FDA-approved once-daily, oral menin inhibitor for the treatment of adults with relapsed or refractory NPM1-mutated acute myeloid leukemia, and continues to pioneer advancements in menin inhibition and farnesyl transferase inhibition.
NewProject Coordinator Catalent Pharma Solutions, Inc.Project CoordinatorChelsea, MA$75,000–$90,000 / yearLocated at 190 Everett Avenue, the approximately 96,000‑square‑foot GMP facility features ISO 8 production suites, high‑potency containment capabilities, and advanced spray drying equipment, including multiple large‑scale GMP spray dryers. Catalent's Chelsea, Massachusetts site-often referred to as the Boston location-is a global Center of Excellence for spray dry dispersion (SDD) and dry powder inhaler (DPI) capsule manufacturing and packaging, supporting inhalation drug products from clinical development through commercial launch.
Administrartive Assitant /Operations Specialist Nurta HHC staffingAdministrartive Assitant /Operations SpecialistLynn, MassachusettsAs an employer accepting Medicare and Medicaid funds, employees must comply with all health-related requirements in all relevant jurisdictions, including required vaccinations and testing, subject to exemptions for medical or religious reasons as appropriate. The Operations Specialist is responsible for providing top-level customer service to internal and external clients as it relates to the branch location’s clinical operational support activities.
Lab Director LabCorpLab DirectorBoston, MA$170,000–$210,000 / yearResolve client inquiries and operational issues in a timely manner by consulting with the Medical Director, Technical Director, QA, other laboratory managers, discipline directors, laboratory managers or corporate operations. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients.
Medical Writing Science Senior Manager (Hybrid) Vertex PharmaceuticalsMedical Writing Science Senior Manager (Hybrid)Boston, Massachusetts$137,200–$205,800 / yearAuthors complex clinical regulatory documents (e.g., clinical study protocols, clinical study reports, investigator’s brochures, documents to support meetings with regulatory agencies, and sections of marketing authorization applications) in partnership with key stakeholders. At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations.
Clinical Director FYZICAL Therapy & Balance CentersClinical DirectorSaugus, MassachusettsAs the Clinical Director, you will play an instrumental role in launching our new clinic, establishing best practices, and fostering a supportive, patient-centered environment as we continue to grow. Nearby Communities (for candidate search purposes): Saugus, Melrose, Wakefield, Stoneham, Winchester, Lynnfield, Peabody, Danvers, Lynn, Revere, Malden, Medford, Everett, Chelsea.
Software Testing Manager Integrated Resources, IncSoftware Testing ManagerCambridge, MassachusettsContractorThe successful candidate must have a proven record of accomplishment, and have prior experience working with a Testing team leading functional testing and automation. • Regular review of Quality Metrics with business and technical teams to drive quality management best practices through all phases of Systems Development Life Cycle.
Associate Director, GMP Operational Quality Vertex PharmaceuticalsAssociate Director, GMP Operational QualityBoston, MassachusettsLeads a team in the Quality Operations organization responsible for internal commercial operations in support of GMP manufacturing and testing activities, including disposition of intermediates, working cell banks and clinical and commercial drug products internally at Vertex manufacturing facilities. Serves as the Quality Lead for assigned clinical programs providing GCP compliance interpretation, consultation, and other support services necessary to maintain and/or improve the quality of Vertex research to ensure the protection of subjects' safety, rights, and well-being as well as the integrity and credibility of data generated.
Associate Director Program Management II Integrated Resources, IncAssociate Director Program Management IILexington, MassachusettsContractorStrong influencing and interpersonal skills including negotiation, managing meetings and group dynamics, ability to balance concerns of line management with objectives of cross-functional team. Strong analytical and decision-making ability, including ability to synthesize complex and diverse inputs to a problem, and recommend solutions/preferred options.
Licensed Independent Clinical Social Worker LICSW Lead Therapist Ellie Mental HealthLicensed Independent Clinical Social Worker LICSW Lead TherapistFoxborough, MassachusettsSo we created a new model: one that puts flexibility, innovative decision-making, creativity, and our people first, while remaining a socially conscious and responsible for-profit business focused on changing how we treat mental health. As an Outpatient Therapist you'll share our vision for improving and expanding access to quality mental health care and thrive in an environment driven by our core values of authenticity, humor, compassion, creativity, acceptance, and determination.
Development Engineer II Integrated Resources, IncDevelopment Engineer IILexington, MassachusettsContractorQualifications: As a member of the Manufacturing Science & Technology group in Process Development department, this individual will join a group of process scientist and engineers to support downstream processes of commercial productions and late stage clinical process development and productions. The scope of work will include designing studies under instruction, executing experiments and data analysis to support GMP investigations and manufacturing change controls and to reduce reoccurring deviations.
Logistics Coordinator Integrated Resources, IncLogistics CoordinatorCambridge, MassachusettsFull timeMust possess excellent organizational, interpersonal and communications skills as well as sensitivity to handling confidential information. Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.
Process Engineer, downstream purification Integrated Resources, IncProcess Engineer, downstream purificationLexington, MassachusettsContractorAs a member of the Manufacturing Science & Technology group in Process Development department, this individual will join a group of process scientist and engineers to support downstream processes of commercial productions and late stage clinical process development and productions. The scope of work will include designing studies under instruction, executing experiments and data analysis to support GMP investigations and manufacturing change controls and to reduce reoccurring deviations.
Procurement/Contract Analyst Integrated Resources, IncProcurement/Contract AnalystCambridge, MassachusettsContractorThe initial responsibilities of this position will include working closely with the global project team to configure the contract system, help to migrate data from the legacy tool and support change management and training across the company. The contract project analyst will be responsible for the day-to-day operations of a large contract management program encompassing the lifecycle of a contract.
Process Engineer I Integrated Resources, IncProcess Engineer ILexington, MassachusettsContractorAs a member of the Manufacturing Science & Technology group, this individual will join a group of process scientists and engineers to support downstream processes of commercial productions and late stage clinical process development and productions. The scope of work will include designing studies under instruction, executing experiments and data analysis to support GMP investigations and manufacturing change controls and to reduce reoccurring deviations.