Supervising Attorney PDD Framingham Committee for Public Counsel ServicesSupervising Attorney PDD FraminghamFramingham, MAThe following attributes are preferred for the position of Supervising Attorney: Significant jury trial experience as lead counsel in criminal cases; including Superior Court cases; Commitment to working with a culturally diverse, low-income population, Willingness and ability to work positively and collaboratively with both the Attorney in Charge and Supervisees; A demonstrated commitment to the principle of zealous advocacy in the representation of indigent persons in criminal cases; Ability and commitment to complete annual performance evaluations in a timely and comprehensive manner; Strong interpersonal and analytical skills; Ability to work in community and defense-oriented capacity, both independently and collaboratively; and, Foreign language skills, Spanish in particular, are desirable. The following attributes are required for the position of Supervising Attorney: Must be eligible to practice law in Massachusetts either as a member of the Massachusetts bar in good standing or as the member of the bar of another jurisdiction eligible to engage in limited Massachusetts practice under Supreme Court Rule 3:04; A minimum of five years of legal experience including at least three years providing criminal defense representation in District and Superior Courts; Access to an automobile in order to travel to courts, clients, and investigation locations that are not easily accessible by public transportation; and, Access to home internet access sufficient to work remotely.
Supervising Administrative Assistant PDD Boston Central Office Committee for Public Counsel ServicesSupervising Administrative Assistant PDD Boston Central OfficeBoston, MAStrong communication, organizational and detail skills; Proficiency in MS Office Suite (Word, Excel, Outlook, PowerPoint); Ability to establish effective working relationships and to work as a team leader; Flexibility, and strict adherence to confidentiality; Typing skill of 50 to 60 wpm preferred; Familiarity with advanced Word formatting and editing, and Microsoft Excel; Legal office experience a plus; and, Foreign language skills are strongly preferred. It is our CPCS mission to achieve these goals, and in furtherance thereof, we embrace and endorse diversity, equity and inclusion as our core values as we maintain a steadfast commitment to: (1) Ensure that CPCS management and staff members represent a broad range of human differences and experience; (2) Provide a work climate that is respectful and supports success; and (3) Promote the dignity and well-being of all staff members.
Senior Medical Director, Oncology Clinical Development - GU GSK plcSenior Medical Director, Oncology Clinical Development - GUWaltham, MA$284,250–$473,750 / yearClinical Data Interpretation, Clinical Pharmacology, Clinical Trial Designs, Clinical Trials Monitoring, Digital Fluency, Drug Development, Drug Regulatory Affairs, Evidence Based Decision Making, Executive Presence, Hematology and Oncology, Learning Agility, Matrix Leadership, Real World Evidence (RWE), Scientific Presentations, Strategic Direction. Use medical expertise to contribute to the end to end (protocol concept to final study report) to ensure scientific integrity and timely delivery of clinical trials which ensure consistency with the clinical development strategy for regulatory approvals, reimbursable medicines, and successful lifecycle management; demonstrate ability to incorporate global considerations into decision making.
Senior Program Manager (SPM) - Mastocytosis SanofiSenior Program Manager (SPM) - MastocytosisCambridge, MA$122,250–$176,583.33 / yearMain Responsibilities: Strategic Partnership & Leadership • Lead program management initiatives for Mastocytosis in strategic partnership with the Medical Program Lead (MPL) • Collaborate with Global Medical Director to operationalize Global Medical Team strategies and deliverables • Drive integrated evidence generation planning through cross-functional partnerships with Global Medical Directors, Brand teams, and functional leads. Operational Excellence & Process Management • Optimize cross-functional communication and decision-making through meeting facilitation and stakeholder engagement • Streamline operational workflows to ensure compliance with internal SOPs and external regulatory guidelines • Utilize harmonized Program Management Tools to manage portfolio-level activities across the Program Management organization.
Supervising Attorney PDD Boston Central & Boston Metro Committee for Public Counsel ServicesSupervising Attorney PDD Boston Central & Boston MetroBoston, MAThe following attributes are preferred for the position of Supervising Staff Attorney: Significant jury trial experience as lead counsel in criminal cases; including Superior Court cases; Commitment to working with a culturally diverse, low-income population, Willingness and ability to work positively and collaboratively with both the Attorney in Charge and Supervisees; A demonstrated commitment to the principle of zealous advocacy in the representation of indigent persons in criminal cases; Ability and commitment to complete annual performance evaluations in a timely and comprehensive manner; Strong interpersonal and analytical skills; Ability to work in community and defense-oriented capacity, both independently and collaboratively; and, Foreign language skills, Spanish in particular, are desirable. The supervisory duties of the Supervising Attorney include, but are not limited to, the following in accordance with the CPCS Guidelines for Supervision of Public Defender Trial Attorneys and the Guidelines for the Implementation of Unified Public Defender Division Offices: Regular one-on-one meetings with individual supervisees to review case files, as well as group meetings, to review case preparation and performance; In-court supervision, including second-seating of trials and significant pretrial hearings; Preparation of annual performance evaluations; Presentation of in-office training sessions; Supervision of other staff, such as investigators and student interns, as delegated by the office's Attorney in Charge; and, Other duties as assigned.
Data Scientist Infectious Disease Tufts UniversityData Scientist Infectious DiseaseBoston, MAResearch topics include structural analysis of virus entry, viral evolution, viral oncogenes, intracellular bacterial pathogens, microorganisms that cause diarrhea and pneumonia, intracellular signaling, pathogen adhesion, genetic determinants involved in susceptibility to infection, vaccine development, and identification of novel antimicrobial agents. Demonstrated expertise in computational biology or a related quantitative discipline, including proficiency in programming languages such as Python, R, or MATLAB, and experience with machine learning frameworks, image analysis pipelines, or statistical modeling of large biological datasets.
Administrative/Project Specialist Point32Health, Inc.Administrative/Project SpecialistBoston, MA$25.83–$38.74 / hourHarvard Pilgrim Health Care Institute is currently seeking a highly motivated Administrative/Project Specialist to join the Therapeutics Research and Infectious Disease Epidemiology group (TIDE) within Harvard Medical School's Department of Population Medicine (www.populationmedicine.org). At Point32Health, we are building on the quality, nonprofit heritage of our founding organizations, Tufts Health Plan and Harvard Pilgrim Health Care, where we leverage our experience and expertise to help people find their version of healthier living through a broad range of health plans and tools that make navigating health and wellbeing easier.
Head of Medical Affairs AVEO Pharmaceuticals IncHead of Medical AffairsBoston, MAREQUIRED QUALIFICATIONS/EXPERIENCE (BASIC QUALIFICATIONS): • Advanced Scientific or Medical degree (s), MD preferred • Demonstrated substantial Medical expertise in Oncology through clinical, research, and business activities • Minimum of 7 years of experience in medical affairs, with 5 years as an MSL in industry; at least 2 years of experience managing an MSL team • Demonstrated success in building effective teams, systems, and processes; proven ability to identify, select and manage a variety of external resources related to execution of medical affairs functions • Ability to lead a team of functional experts and negotiate the multi-disciplinary environment in which they operate • Strategic and analytical thinking with the ability to contribute to the plan and design effective medical affairs brand and life cycle strategies • Strong understanding of industry and regulatory guidelines pertinent to compliant interactions with external audiences • Demonstrated ability to comprehend complex scientific, medical, and relevant business issues and respond with actionable strategies and tactics to effectively produce timely and measurable results • Excellent written and verbal communication skills, exceptional listening skills, strong presentation skills, and good negotiating and influencing skills. JOB SUMMARY: Reporting to the CEO/CMO, the Head of Medical Affairs will serve as the functional manager and leader of the Field-based Medical Science Liaison team and provide strategic input into key medical affairs activities, including consistent and aligned medical and scientific communications, cross-functional medical strategy, development and execution of Advisory Boards, KOL and other key customer identification and engagement, publication strategy and planning, CME topics of interest and grant administration, and fostering relationships with key societies, physician networks, oncology cooperative groups and academic institutions.
Postdoctoral Fellow in Psychology Harvard UniversityPostdoctoral Fellow in PsychologyCambridge, MA$67,600–$80,000 / yearThe Postdoctoral Fellow will have the opportunity to collaborate with an interdisciplinary team including Ila Fiete (MIT), Aude Olive (MIT), Pulkit Agrawal (MIT), and Pieter Abbeel (UC Berkeley). $67,600 - $80,000 The pay offered to the selected candidate is dependent on factors such as years of experience, training, or qualification, field of scholarship, and accomplishments in the field.
Global Safety Lead - Formulation Safety CSL Behring LLCGlobal Safety Lead - Formulation SafetyWaltham, MAOversees analysis of aggregate safety data and the production of key company documents such as DSURs (Development Safety Update Reports), PSURs (Periodic Safety Update Reports) and risk management plans relating to the safety of medicinal products, which are subject to regulatory review and discussion. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.
Laboratory Coordinator - Biology Tufts UniversityLaboratory Coordinator - BiologyMedford, MAThe Tufts Department of Biology is dedicated to providing for our students a unified and comprehensive view of biological processes and opportunities for undergraduates to actively participate in cutting-edge biological research in molecular biology, cell biology, genetics, physiology, plant ecology, animal behavior, and conservation biology. The Department of Biology maintains an active research and teaching program on the Medford campus and in various field locales and trains and advises graduate and undergraduate students as well as post-doctoral fellows.
Postdoctoral Research Associate - Medical Device Wound Healing UMass LowellPostdoctoral Research Associate - Medical Device Wound HealingLowell, MassachusettsSkills: Demonstrated excellence in one or more of the following areas is required: control systems, mechanical design, electromechanical system fabrication, rapid prototyping, miniature sensors development, electronic circuit design, CAD design, programming in LabVIEW, LabVIEW Real-Time (software and hardware). The project is sponsored by the Defense Health Agency through the US Combat Casualty Care Research Program and in collaboration with investigators at Massachusetts General Hospital and Harvard Medical School.
Laboratory Research Assistant UMass LowellLaboratory Research AssistantLowell, MassachusettsGeneral Summary of Position: Under the supervision of the Principal Investigator, the Laboratory Research Assistant is responsible for supporting research projects that aim to understand how genetics affects lactation through participating in research activities including mammalian cell culture, molecular assays, imaging, laboratory organization, reagent preparation, and experimental workflows. Essential Job Duties: Maintain mammalian cell cultures (under minimal supervision): Prepare sterile media, buffers, reagents, and cell culture supplies for multiple cell lines, perform routine cell passaging, cryopreservation, and viability assessments.
Senior Scientist, Clinical Research Merck & Co IncSenior Scientist, Clinical ResearchBoston, MA$117,000–$184,200 / yearCo-authors clinical sections of protocols, clinical investigator brochures, clinical study reports, Worldwide Marketing Application/Common Technical Document (WMA/CTD) subsections, and regulatory agency update and safety reports, as well as clinical development plans, publications, and abstracts. Experience managing Immunology and/or vaccine trials with an ability to think outside of the box, explore novel ways of working and comfortably navigate ambiguity to drive results also a plus.
US Medical Director, Advanced Systemic Mastocytosis (Asm) SanofiUS Medical Director, Advanced Systemic Mastocytosis (Asm)Cambridge, MA$178,500–$257,833.33 / yearThe Medical Director will establish and maintain collaborative medical and scientific relationships with key external physicians and internal constituencies from multiple functional groups including, but not limited to, Medical Affairs, Clinical Research, Regulatory, Science, Marketing, Sales, Commercial Operations, and Patient and Product Services - while maintaining full compliance with all relevant company, industry, legal, and regulatory requirements. The mission of this team is to support the company by functioning as the internal expert in rare blood disorders and therapies and helping Health Care Professionals and Payers optimize patient care and treatment outcomes through evidence-based decisions.
New["Investigations Manager 2: Professional Standards Leader - Flexible Hours","Investigations Manager 2: Professional Standards Leader - Flexible Hours"] State of Oregon["Investigations Manager 2: Professional Standards Leader - Flexible Hours","Investigations Manager 2: Professional Standards Leader - Flexible Hours"]SalemYou will supervise investigators, advise senior management, manage complex studies and legislative relations, and promote trauma-informed, equitable practice across Oregon's juvenile justice#J-18808-Ljbffr.
NewAcademic Partnerships Director Beacon Biosignals IncAcademic Partnerships DirectorBoston, MARemoteBeacon Biosignals is seeking a scientifically and clinically credentialed, relationship-driven Academic Partnerships Director to grow adoption of the Beacon Platform, including the research use of its medical devices, within academic and research institutions. As such, we're always seeking new contributors whose work demonstrates an avid curiosity, a bias towards simplicity, an eye for composability, a self-service mindset, and, most of all, a deep empathy towards colleagues, stakeholders, users, and patients.
Senior Clinical Studies Associate DeephealthSenior Clinical Studies AssociateSomerville, Massachusetts$71,000–$96,000 / yearFull timeWorking under the guidance of Clinical Study Manager and cross-functional study teams, the SCSA contributes to study operations, documentation, regulatory compliance, and process improvement initiatives. This position often requires sitting, standing, walking, bending, twisting, reaching with hands and arms, using hands and fingers, handling, or feeling, speaking, listening, and high-level cognitive thinking.
Clinical Study Quality Lead, Associate Director Vertex PharmaceuticalsClinical Study Quality Lead, Associate DirectorBoston, Massachusetts$160,600–$240,800 / yearOverall, the SQL is responsible for the development and execution of audit/quality plans, accurately identifying and communicating compliance risks and overseeing action plans to mitigate risks, real-time study inspection readiness oversight, and collaboratively identifying and driving inspection preparedness strategies and activities. Provides strategic, risk-based GCP quality compliance oversight of studies within assigned disease areas to drive compliance with regulatory requirements to ensure the protection of participants’ safety, rights, and well-being as well as the integrity and credibility of study data generated.
Clinical Pharmacology Director Sumitomo Pharma America Holdings Inc (Inactive)Clinical Pharmacology DirectorMarlborough, MA$190,500–$238,100 / yearSumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. Lead Phase 1 and special population clinical pharmacology studies (e.g., FIH, SAD, MAD, DDI, organ impairments, elderly/pediatric, PET/EEG), including protocol input, operational oversight, and interpretation and communication of results.