• Biogen (Weston, MA)
    …Job Description The US Senior Medical Director will lead all medical pre-launch and launch activities in US for the pipeline portfolio with an initial specific focus ... in ophthalmology and stroke. This leader will report to the VP and head of US medical. Job Responsibilities Responsible for leading the strategic design and execution of ophthalmology and stroke medical plan and tactics within US. Collaborate with the Global… more
    Neuvoo (07/01/20)
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  • Biogen (Cambridge, MA)
    …Job Description We have an exciting new opportunity for an Associate Director, Real World Evidence Strategy and Analytics to join our team in Cambridge, MA. In this ... role, youll be responsible for providing biostatistical support and guidance on RWE studies and may serve as the responsible RWE biostatistician on several RWE projects in different indications. This role reports into the Director, Real World Evidence Strategy… more
    Neuvoo (07/01/20)
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  • Biogen (Cambridge, MA)
    …Job Description The Associate Medical Director is responsible for overseeing and defining the data generation strategy and priorities for the NM disease therapeutic ... area. The Associate Medical Director will work closely with the MERI organization to ensure adequate execution of the data generation plans and cross-functionally to align on the strategic priorities. The Associate Medical Director is the key driver for… more
    Neuvoo (07/01/20)
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  • Biogen (Weston, MA)
    …Job Description The Senior Medical Value Liaison engages in peer to peer scientific and health economic discussions with top tier national and regional payors and ... relevant regional external health care access decision makers (HCDMs) and influencers at US public and private payors and related entities including, but not limited to, managed care organizations (MCOs), specialty pharmacy providers (SPPs), pharmaceutical… more
    Neuvoo (07/01/20)
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  • Biogen (Weston, MA)
    …Job Description The Senior Director of Medical Value Strategy and Execution (MVSE) in US Medical will lead the medical payor engagement strategy across all ... therapeutic areas including pipeline and work closely with cross functional partners in US & Global Medical (eg MA&R, MERI, Value & Access) to demonstrate the value proposition of medicines to enable optimal market access, reimbursement and brand growth for… more
    Neuvoo (07/01/20)
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  • Takeda (Boston, MA)
    …Are you looking for a patient-focused company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join us as ... an Asc Dir CQA Program Lead in our Cambridge office. Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. As an Asc Dir CQA Program Lead working on the R&D Quality team, you will be empowered to lead Clinical Quality… more
    Neuvoo (06/30/20)
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  • Covance (Boston, MA)
    …include; * Medical and safety monitoring; Medical data review * Develop, review, and revise protocols, CRF, training materials, code/data tables, listing and figures ... * Actively participates and assists in preparations for investigator meetings * Participates in project risk assessment activities * Provides clinical and medical expertise to other Covance departments * Contributes to the scientific strategic leadership for a… more
    LinkUp (06/30/20)
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  • CorTech LLC (Worcester, MA)
    …The ligand binding assay (LBA) group in the DMPK Department at Bioresearch Center in Worcester, MA, supports immunology discovery programs on biologics therapeutics. ... In addition, the LBA group has global responsibilities in providing non-GLP LBA bioanalysis support for biologics projects across all therapeutic areas at client. The Scientist I/II will perform LBA method development to support non-GLP pharmacokinetics,… more
    JobsRUs (06/29/20)
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  • PerkinElmer (Waltham, MA)
    …Technically contribute to multiple projects developing reagent kits for molecular diagnostics Hands-on involvement in molecular assay development, verification and ... validation Own and drive technical sub-projects as needed to guarantee overall project success Present experimental findings and interpretations to R&D team members Actively contribute to technical root cause activities to identify and alleviate roadblocks… more
    Neuvoo (07/01/20)
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  • AbbVie (Cambridge, MA)
    …Set the global strategy for Neuroscience Computational Biology for target identification and biomarker research in close alignment with AbbVie''s Neuroscience ... objectives. Shape innovative approaches to drive the Neuroscience portfolio forward and bridge across all R&D, including but not limited to integration of OMICS data especially single cell level technologies, translational biomarker research, genomics cohort… more
    Neuvoo (07/01/20)
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  • Biogen (Weston, MA)
    …Company Description Job Description The Senior Medical Value Liaison engages in peer to peer scientific and health economic discussions with top tier national and ... regional payors and relevant regional external health care access decision makers (HCDMs) and influencers at US public and private payors and related entities including, but not limited to, managed care organizations (MCOs), specialty pharmacy providers… more
    ZipRecruiter (06/17/20)
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  • Biogen (Cambridge, MA)
    …Company Description Job Description We have an exciting new opportunity for an Associate Director, Real World Evidence Strategy and Analytics to join our team in ... Cambridge, MA. In this role, you'll be responsible for providing biostatistical support and guidance on RWE studies and may serve as the responsible RWE biostatistician on several RWE projects in different indications. This role reports into the Director, Real… more
    ZipRecruiter (06/12/20)
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  • Kelly Scientific Resources (Burlington, MA)
    …Verify compliance according to Validation Master Plan requirements Review of IQ, OQ, and PQ packages Review unexecuted and executed batch records for compliance with ... internal specifications Investigate manufacturing validation-related Deviations, Change Controls, Investigations, and CAPA Review and approve document changes for SOPs, test methods, raw materials, protocols, and batch records Performs internal and external… more
    Neuvoo (07/01/20)
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  • Talentify (Cambridge, MA)
    …Are you looking for a patient-focused company that will inspire you and support your career? If so, be empowered to take charge of your future atJob Requirements: ... Takeda. Join us as a Senior Director/Head of Global Medical Communications in our Cambridge, MA location. Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. As a Director/Group Lead, working on the Global Medical… more
    Neuvoo (07/01/20)
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  • Careerbuilder-US (Waltham, MA)
    …* Provide clinical study level data management oversight of outsourced clinical trials for phase I / II studies including: project management, vendor management, ... coordination of internal reviews, and approval of deliverables. * Oversee database design and production, ensuring that CROs, vendors and internal staff meet the highest quality standards, ensuring complete, correct and consistency of clinical data and… more
    Neuvoo (07/01/20)
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  • PerkinElmer (Andover, MA)
    …contribute to multiple projects developing reagent kits for molecular diagnosticsHands-on involvement in molecular assay development, verification and validationOwn ... and drive technical sub-projects as needed to guarantee overall project successPresent experimental findings and interpretations to R&D team membersActively contribute to technical root cause activities to identify and alleviate roadblocks internally and with… more
    JobDiagnosis (07/01/20)
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  • Giant Eagle (Hudson, MA)
    …Maintain proper inventory levels by submitting on line order, adding and adjusting order points, order quantities and on-hand counts in the computer and assisting ... manager in preparation of physical inventories Maintain a neat and clean work environment to ensure Company and government requirements are met. File written prescriptions daily. Assist Team Members with tasks to ensure department runs efficiently. Review all… more
    JobToMe (07/01/20)
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  • Morphic Therapeutic (Waltham, MA)
    …The Clinical Trial Manager will be responsible for the implementation and conduct of clinical trials. These activities include site feasibility analysis and ... About Morphic Therapeutic Morphic Therapeutic is a biopharmaceutical company developing a new generation of oral integrin therapies for the treatment of serious chronic diseases, including inflammatory, hepatic, fibrosis, cardio-pulmonary, and cancer. In… more
    PandaLogic (07/01/20)
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  • Karyopharm Therapeutics Inc. (Newton Center, MA)
    …This person will be responsible for the planning, identification, coordination, execution, reporting and closure of CGP Compliance issues in support of clinical ... programs. The incumbent is also responsible for supporting the GCP auditing plan and assisting its management. Conduct Regulatory Submission Review such as Investigator Brochures (IB), Development Safety Update Report (DSUR), Clinical Study Reports (CSRs),… more
    JobDiagnosis (07/01/20)
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  • Karyopharm Therapeutics Inc. (Newton Center, MA)
    …in developing strategy and development of regulatory submission documentsProvide regulatory expertise and support nonclinical and clinical areas for investigational ... productsEnsure clinical and nonclinical programs are designed and implemented to meet regulatory requirementsComplete documents and other assigned tasks within established timelines and with high quality - in terms of scientific content, organization, clarity,… more
    JobDiagnosis (07/01/20)
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