Tufts Medicine Research/Clinical Cluster Hire Tufts MedicineTufts Medicine Research/Clinical Cluster HireBoston, MA$107,260–$256,000 / yearThe Tufts Clinical and Translational Science Institute (CTSI) has active shared research and education programs with Jackson Laboratories, Maine Medical Center, MIT, Northeastern University, and other partners. Be able to articulate a vision of how their expertise can integrate with existing assets at Tufts to collaboratively and impactfully address unmet needs in biomedical science and clinical medicine.
Per Diem- Clinical Research Assistant Boston Children's HospitalPer Diem- Clinical Research AssistantBoston, MA$22.35–$35.76 / hourTo qualify, you must have a bachelor's degree in a related field, a high attention to detail and organizational skills, ability to multitask, analytical skills to gather and interpret data, and well-developed communication skills. Coordinating and supporting preparation of the necessary documentation for Institutional Review Board (IRB) and Committee on Clinical Investigations (CCI) submissions, together with the research study team.
Clinical Research Assistant Boston Children's HospitalClinical Research AssistantBoston, MA$46,488–$74,380.80 / yearDr. Shimamura leads several international registries and research studies focused on improving diagnosis and treatment for bone marrow failure disorders including Shwachman-Diamond syndrome, severe chronic neutropenia, aplastic anemia, and others. Assist in developing supportive study documents such as informed consent forms, monitoring templates, study subject tracking tools, monitoring forms, study manuals, and training materials, as required for a study.
Field Clinical Product & Research Specialist (FCPRS) H/F/X TissiumField Clinical Product & Research Specialist (FCPRS) H/F/XCambridge, MassachusettsCollaborate with Study Management and other clinical operations staff to perform site management and field monitoring activities: Establish and maintain excellent working relationships with external stakeholders such as Investigators, Study Coordinators and other site staff; and internal stakeholders to meet recruitment targets and to deliver high-quality data on time. Additionally, FCPRS may be requested to support field-based clinical support by providing information and training to customers in the use of specific products in a clinical setting (e.g., operating room, outpatient clinic, etc.).
CRC- Clinical Research Coordinator Alcanza Clinical Research LLCCRC- Clinical Research CoordinatorMAScheduling subjects for study visits and conducts appointment reminders; Building/updating source as needed; Conducting monitoring visits and resolves issues as needed in a timely manner; Ensuring study related reports and patient results are reviewed by investigator in a timely manner; Filing SAE/Deviation reports to Sponsor and IRB as needed; Documenting and reporting adverse events; Reporting non-compliance to appropriate staff in timely manner; Maintaining positive and effective communication with clients and team members; Always practicing ALCOAC principles with all documentation; May assist with study recruitment, patient enrollment, and tracking as needed; Maintaining confidentiality of patients, customers and company information, and; Performing all other duties as requested or assigned. Responsibilities may include but are not limited to: Screening of patients for study enrollment; Patient consents; Patient follow-up visits; Documenting in source clinic charts; Entering data in EDC and answers queries; Obtaining vital signs and ECGs; May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; Requesting and tracking medical record requests; Updating and maintaining logs, chart filings; Maintaining & ordering study specific supplies;].
Clinical Research Coordinator II - Lowell General Hospital, Cancer Center - On-site Tufts MedicineClinical Research Coordinator II - Lowell General Hospital, Cancer Center - On-siteLowell, Massachusetts$47,924.24–$59,894.75 / yearThe Clinical Research Coordinator supports clinical trials by recruiting and screening participants, conducting informed consent, and coordinating all protocol‑required visits, procedures, and follow‑up. Responsible for assisting with Institutional Review Board (IRB) requirements for each study including meeting institutional educational requirements, submitting documents for review, adverse event reporting and annual reviews.
Clinical Trial Associate or Senior Clinical Trial Associate Kymera TherapeuticsClinical Trial Associate or Senior Clinical Trial AssociateWatertown, MA$115,000–$200,000 / yearHaving advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Work closely with translational medicine team to ensure appropriate incorporation of bioanalytical sampling plan into clinical protocols and relevant data output of the trial is provided to functional groups for review.
Postdoctoral Research Fellow - Molecular Cardiology Research Institute Good Lab Tufts MedicinePostdoctoral Research Fellow - Molecular Cardiology Research Institute Good LabBoston, MA$55,883.46–$69,859.61 / yearThe laboratory uses state of the art molecular and cellular biology assays, ex vivo vascular function studies, and state-of-the-art mouse models of vascular injury and ischemic injuries to address clinically relevant questions in vascular biology and physiology. The lab focuses on evaluating the role and regulation of Pannexin 1, a potential novel therapeutic target, within arterial and venous endothelial cells and how it contributes to the etiology of ischemic injuries and vascular-mediated progression of Alzheimer Disease.
Senior Clinical Data Manager Tango TherapeuticsSenior Clinical Data ManagerBoston, MA$144,800–$217,200 / yearEnsure timely delivery of complete, accurate, reliable, and inspection-ready clinical data through effective oversight of outsourced Data Management activities, including EDC, IRT and eCOA system build, validation and maintenance, data collection, data cleaning, medical coding, external data integration and reconciliation, database/system lock, and submission readiness. Review and approve key Data Management deliverables, including CRF/eCRF, IRT, eCOA specifications, edit checks, Data Management Plans, CRF completion guidelines, data transfer specifications, external data reconciliation plans, and other study-specific documentation.
Corporate Quality and Clinical Auditor Hologic IncCorporate Quality and Clinical AuditorMarlborough, MASupport clinical audit activities for recently acquired companies or products, maintain and update the electronic audit module, assess external regulatory trends, and provide strategic updates on clinical compliance performance. This role develops and maintains audit electronic audit systems, analyzes data for reporting, and supports risk-based and special audits, including those related to new acquisitions and transfers.
Cannabis Fulfillment Specialist, MA Ethos CannabisCannabis Fulfillment Specialist, MABoston, MA$20–$22 / hourFull timePosition Summary/ObjectiveThe Fulfillment Specialist is responsible for processing and fulfilling orders and assisting with maintaining the smooth flow of medical cannabis from intake to point-of-sale, while maintaining a stellar online menu for optimum patient satisfaction and education. Fulfillment SpecialistMassachusettsWebsite: www.ethoscannabis.comCompany OverviewEthos Cannabis currently has interests in the cultivation, processing and dispensing of cannabis in Pennsylvania, Massachusetts, Ohio, and is pursuing expansion opportunities.
Senior Programmer, Clinical Data Evaluation CSL Behring LLCSenior Programmer, Clinical Data EvaluationWaltham, MA$143,000–$169,000 / yearWe 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. Focused on serving patients' needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas.
Director, Clinical Pharmacology Modelling and Simulation (CPMS) Oncology GSK plcDirector, Clinical Pharmacology Modelling and Simulation (CPMS) OncologyWaltham, MA$188,100–$313,500 / yearWe are seeking professionals with the following required skills and qualifications to help us achieve our goals: PhD in Quantitative Clinical Pharmacology and Pharmacometrics disciplines (e.g., pharmacology, engineering or statistics) and experience in using modeling/simulation to solve practical problems in industry or academia. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients' needs and have the highest probability of success.
Senior Director -Project Toxicologist - Clinical Pharmacology and Safety Sciences (Boston or Gaithersburg) AstraZeneca PlcSenior Director -Project Toxicologist - Clinical Pharmacology and Safety Sciences (Boston or Gaithersburg)Boston, MA$227,602–$341,404 / yearExtensive experience working as a Project Toxicologist across different therapy areas within the pharmaceutical/biotech project environment delivering pre-clinical toxicology packages and successful marketing for a range of modalities which should include small molecules, peptides and oligonucleotides. We value kindness alongside ambition, giving you the trust, tools, and cross-functional partnerships to lead with confidence and shape studies that matter-so your decisions today translate into meaningful patient impact tomorrow.
Senior Clinical Trial Manager, Cambridge, MA Isomorphic Labs LimitedSenior Clinical Trial Manager, Cambridge, MACambridge, MASupport data management activities such as reviewing study-related materials created by data management, including the study manual, edit check manual, clean patient data tracker, listing review process and the Statistical Analysis Plan. By harnessing AI's powerful capabilities, we can use it to model complex biological phenomena to help design novel molecules, anticipate how drugs will perform and develop innovative medicines to treat and cure some of the world's most devastating diseases.
Senior Research Program Manager Beth Israel Lahey HealthSenior Research Program ManagerBoston, Massachusetts$95,000–$135,000 / yearSpecific key initiatives that the Program Director will support are: (1) management and oversight of research operations including interdigitation with central grants administration, contractual agreements, and financial oversight; (2) supporting the recruitment and onboarding of new faculty and staff and management of biostatistical and research staff groups; (3) strategy, direction, and programmatic support for academic initiatives to facilitate the continued growth of the research program, including the promotion and expansion of philanthropic and grant base, and coordination of academic programs such as research seminars, pilot grants, and the career mentorship program. The position partners with the Director of Research, Chief of Cardiology, BIDMC Research Administration, individual Principal Investigators, and a small team of Research Program Coordinators and Administrators to optimize research operations, assist in management of research personnel, and develop strategic initiatives including training and career development within the CVI.As a key partner to the leadership team, the Sr.
NewManager, Clinical Study Operations Beacon Biosignals IncManager, Clinical Study OperationsBoston, MA$115,000–$135,000 / yearManage Beacon''s day-to-day working relationship with sponsors - and, where applicable, a CRO intermediary - on the studies your direct reports run, and step in to represent Beacon directly with the sponsor when a study lead escalates a decision that needs strategic alignment or sign-off. You are expected to bring hands-on clinical trial operations experience - enough to guide your direct reports through site and vendor issues, coach sound day-to-day tradeoffs, and step in directly on complex or high-stakes situations when needed.
Senior Specialist, Quality Assurance Investigations, Cell Therapy, Devens - MA Bristol-Myers Squibb CoSenior Specialist, Quality Assurance Investigations, Cell Therapy, Devens - MAMA$89,780–$108,789 / yearBased on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
Biostatistician CareerscapeBiostatisticianBoston, MA$58–$78 / hourContractorThis contract role involves designing statistical analysis plans, analyzing clinical trial data, and producing reports that support regulatory submissions. This is a contract engagement suited to a candidate who can work independently, manage competing deadlines across several studies, and communicate statistical findings clearly to non-technical stakeholders.
Senior Clinical Data Manager Tango Therapeutics IncSenior Clinical Data ManagerBoston, MA$144,800–$217,200 / yearEnsure timely delivery of complete, accurate, reliable, and inspection-ready clinical data through effective oversight of outsourced Data Management activities, including EDC, IRT and eCOA system build, validation and maintenance, data collection, data cleaning, medical coding, external data integration and reconciliation, database/system lock, and submission readiness. Review and approve key Data Management deliverables, including CRF/eCRF, IRT, eCOA specifications, edit checks, Data Management Plans, CRF completion guidelines, data transfer specifications, external data reconciliation plans, and other study-specific documentation.