Medical Affairs/Safety- Director, Product Lead MD LancesoftMedical Affairs/Safety- Director, Product Lead MDCambridge, MA$210Lead active monitoring and continued assessment of safety profile through systematic signal detection and critical review of aggregate safety data and literature during all phases of the life-cycle of a defined portfolio of products. Serve as the safety expert providing strategic input to key stakeholders in relation to product safety, understanding the business strategy for the product, and being knowledgeable about the (medical) context of the respective product class.
Patient Liaison (Patient Recruiter) Alcanza Clinical Research LLCPatient Liaison (Patient Recruiter)MAEssential Job Duties: Execute onsite patient pre-screening and a focus on pivoting qualified patients into active studies for dedicated and local sites should patient be willing to travel. Minimum Qualifications: A high school diploma, or equivalent, AND a minimum of 5 years' experience in a healthcare, call center, or medical research environment, or a similar field, or an equivalent combination of education and experience, is required.
Associate Director, Nonclinical Development Avalyn PharmaAssociate Director, Nonclinical DevelopmentBoston, Massachusetts$179,000–$202,000 / yearReporting to the VP, Translational Sciences, the role requires strong pharmacology expertise, excellent scientific judgment, and exceptional technical writing skills to effectively synthesize and communicate complex data to cross-functional teams, regulatory agencies, and external stakeholders. AP01 has demonstrated encouraging safety and clinical activity across Phase 1b and an ongoing, multi-year open-label extension trial, with long-term data supporting the potential to preserve lung function while improving tolerability relative to historical oral pirfenidone.
Cornea, External Disease, & Refractive Surgery Specialist - Tufts Medical Center Tufts MedicineCornea, External Disease, & Refractive Surgery Specialist - Tufts Medical CenterBoston, MA$135,344–$278,881 / yearThis historic city is known for its outstanding academic institutions, excellent public and private schools, miles of coastal and island beaches, proximity to New Hampshire and Vermont mountains for skiing and outdoor activities, local arts and cultural attractions including the Boston Symphony, Museum of Fine Arts, and professional sporting teams with the Boston Red Sox, Celtics, Bruins, New England Patriots and Revolution. The chosen candidate will have the opportunity to see patients at TMC in Boston, teach residents and medical students, participate in academic research, as well as provide care at our satellites and affiliated partners in nearby suburban, private practice locations.
Laboratory Supervisor - Blood Bank Labcorp Holdings IncLaboratory Supervisor - Blood BankBoston, MA$90,000–$120,000 / yearLabcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. 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.
Pre-Licensed Child & Adolescent Therapist Remote, MA InStride Health IncPre-Licensed Child & Adolescent Therapist Remote, MAMARemoteWe are doing this by combining research-backed clinical care and innovative technology to eliminate the major problems with care today: difficulty finding providers, months of waiting to be seen, arduous onboarding processes, and inconsistent use of evidence-based therapies and outcomes tracking. We are looking for a virtual Pre-Licensed Therapist to join our team to deliver family-centric and evidence-based care to Children, Adolescents, & Young Adults.
Histology Supervisor Labcorp Holdings IncHistology SupervisorBoston, MA$90,000–$125,000 / yearLabcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. 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.
Transplant Hepatologist Tufts MedicineTransplant HepatologistBoston, MA$300,000–$525,000 / yearFollowing the successful relaunch of its Liver Transplant Program, Tufts Medical Center has achieved several significant milestones, including CMS certification of the Liver Transplant Program and approval from the Organ Procurement and Transplantation Network (OPTN) to launch a Living Donor Liver Transplant Program. Comprised of Tufts Medical Center, Lowell General Hospital, MelroseWakefield Hospital, Lawrence Memorial Hospital of Medford, an expansive home care network, and a large integrated physician network, Tufts Medicine provides more than 1.5 million patient experiences each year.
Sr. Manager, Medical Affairs - Evidence Generation and Data Insights Insulet CorpSr. Manager, Medical Affairs - Evidence Generation and Data InsightsActon, MA$156,100–$234,100 / yearProvide biostatistical support to prospective clinical trials as needed, including input on study design, sample size and power calculations, randomization and endpoint definitions, authoring and execution of statistical analysis plans, and statistical interpretation and reporting of results in clinical study reports and regulatory submissions. Serve as a technical expert to cross-functional teams to identify evidence needs and how research studies and RWD can be used to support the product development and commercialization strategy; contribute to the development, maintain, and expand a portfolio of RWD research activities to support these strategies.
NewResearch Scientist, Molecular AI Takeda PharmaceuticalResearch Scientist, Molecular AIBoston, MA$116,000–$182,270 / yearThe actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. D. in Computational Biology, Biophysics, Computer Science, Computational Chemistry, or a related field, with a research focus in ML for molecular modeling (e.g., structure prediction, co-folding, affinity, or molecular design).
NewClinical Professional Development Specialist - Birthing & Mother Infant Units South Shore HealthClinical Professional Development Specialist - Birthing & Mother Infant UnitsWhitman, MA$100,000–$199,999 / yearRequired Licenses / Registrations RN - Registered Nurse Certifications (determined by division) may include: • BLS- Basic Life Support • ACLS– Advanced Cardiac Life Support • NRP-Neonatal Resuscitation Program • PALS- Pediatric Advanced Life Support • TNCC- Trauma Nurse Core Course Instructor level certification required for certain divisions and may include (but not limited to): • AHA BLS instructor • AHA ACLS instructor Achieving Professional Certification is an expectation once eligibility criteria are met. *** Prior Birthing Unit experience strongly preferred as is MSN (completion and/or currently in process) *** ***AWHONN Fetal Monitoring Instructor strongly preferred*** The Clinical Professional Development Specialist (CPDS) is responsible for leading and educating nursing division initiatives, and participating in inter-professional quality initiatives.
NewMedical Science Liaison, Breast Oncology - Northeast Daiichi Sankyo, Inc.Medical Science Liaison, Breast Oncology - NortheastBoston, MI$153,600–$230,400 / yearFull timeIdentifying and appropriately facilitating engagement of qualified 1) investigators and study committee members for DSI clinical research programs, 2) investigator-initiated research study proposals, 3) speakers for DSI Brand Speaker programs, 4) advisors for DSI scientific, clinical and marketing advisory boards. The MSL develops skills and competencies to educate healthcare professionals, DSI internal stakeholders (e.g., Medical, Marketing, and Sales), and decision makers in healthcare systems regarding therapeutic areas and related products developed and commercialized by DSI.
Senior Clinical Research Associate/Clinical Research Associate II - Oncology - US Any Region - FSP ParexelSenior Clinical Research Associate/Clinical Research Associate II - Oncology - US Any Region - FSPMassachusettsPartner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients; provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks. Submit all required reports, documentation, updates and tracking within required timeframes, including but not limited to Trial Master File (TMF) documentation, site reports, site follow up letters, protocol deviations, patient recruitment, clinical supply management, study progress and metrics.
Clinical Research Associate - Full-Service Syneos Health IncClinical Research Associate - Full-ServiceMATogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
Clinical Research Systems Specialist Iterative HealthClinical Research Systems SpecialistCambridge, MA$23–$40 / hourA Clinical Research Systems Specialist at Iterative Health plays an important role in enabling our clinical research operations by ensuring the systems, study builds, and operational materials that support our trials are accurate, efficient, and ready for use by our teams and research sites. We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology.
Clinical Research Systems Specialist Iterative Scopes IncClinical Research Systems SpecialistCambridge, MA$23–$40 / hourA Clinical Research Systems Specialist at Iterative Health plays an important role in enabling our clinical research operations by ensuring the systems, study builds, and operational materials that support our trials are accurate, efficient, and ready for use by our teams and research sites. We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology.
NewPrincipal Research Associate, Clinical Biomarker Laboratory Moderna IncPrincipal Research Associate, Clinical Biomarker LaboratoryNorwood, MA$89,900–$143,800 / yearParticipate in review of protocols, methods, reports, batch records and related GLP/GcLP source documents to actively manage data and documents by using various software like Excel, LabVantage LIMS (Laboratory Information Management System) database for clinical phase studies. The Principal Research Associate will work closely with the clinical Biomarker Laboratory Lead, biostatisticians, Quality/ Compliance partners, and other cross-functional stakeholders to deliver high-quality, traceable, and regulatory-compliant bioanalytical data supporting Vaccine clinical development programs.
Sr. Research Associate, Clinical Biomarker Laboratory, Flow Cytometry Moderna IncSr. Research Associate, Clinical Biomarker Laboratory, Flow CytometryNorwood, MA$74,000–$118,400 / yearWe are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. The Role: Moderna is seeking a talented and motivated Senior Research Associate to join the Clinical Flow Cytometry group to serve as a technical expert for the generation of high parameter flow cytometry data under GCLP guidelines to support clinical programs across multiple therapeutic areas.
Clinical Research Program Manager The Shriners Hospital for ChildrenClinical Research Program ManagerBoston, MassachusettsReporting to the Hospital Administrator and Research Programs Office at SHC International Headquarters, the CRPM provides support and leadership in accordance with SHC's policies and procedures, SHC's hospital regulations, the Code of Federal Regulation, and Good Clinical Practice guidelines, when applicable. The CRPM works closely with the Chief of Staff, SHC scientific and medical staff and other research personnel to ethically recruit and consent SHC's vulnerable pediatric subjects and to appropriately collect and safeguard data.
Sr. Research Associate, Clinical Biomarker Laboratory Moderna IncSr. Research Associate, Clinical Biomarker LaboratoryNorwood, MA$74,000–$118,400 / yearThis laboratory-based role will support the development, qualification, validation, transfer, and clinical implementation of cell-based assays, virus neutralization/functional antibody assays, and ligand-binding assays (LBAs) used to characterize vaccine-induced immune responses and support clinical vaccine development programs, while also contributing to biomarker and immunogenicity testing across Moderna's infectious disease, oncology, and autoimmune disease portfolio. The successful candidate will bring strong hands-on experience with mammalian cell culture, cell-based functional assays, and immunoassays and will be expected to independently execute assay development and optimization experiments, qualification/validation studies, clinical sample testing, data analysis, troubleshooting, and compliant documentation in a regulated clinical laboratory environment.