Medical Science Liaison - Gastroenterology - Southwest SanofiMedical Science Liaison - Gastroenterology - SouthwestCambridge, MARemote$146,250–$211,250 / yearCritically and routinely evaluate and discern from the information gained from published studies, and stakeholder interactions to develop key insights that deepen our understanding of the market's needs and opinions of external stakeholders and therefore contribute to enhancement of Sanofi's scientific messages, plans, strategy, systems, and product development. The Medical Science Liaison (MSL) is field-facing role whose main objectives are to: Be the trusted scientific partner to key external experts by conducting timely, appropriate and frequent scientific exchanges to enhance the understanding of the scientific and medical value of our products.
Medical Science Liaison - Gastroenterology - West SanofiMedical Science Liaison - Gastroenterology - WestCambridge, MA$146,250–$211,250 / yearCritically and routinely evaluate and discern from the information gained from published studies, and stakeholder interactions to develop key insights that deepen our understanding of the market's needs and opinions of external stakeholders and therefore contribute to enhancement of Sanofi's scientific messages, plans, strategy, systems, and product development. Main Responsibilities: The Medical Science Liaison (MSL) is field-facing role whose main objectives are to: Be the trusted scientific partner to key external experts by conducting timely, appropriate and frequent scientific exchanges to enhance the understanding of the scientific and medical value of our products.
Clinical Research Assistant Opportunities - Multiple Locations Nationwide Headlands ResearchClinical Research Assistant Opportunities - Multiple Locations NationwidePlymouth, MAThis general interest posting is designed for Clinical Research Assistants (RAs) who may not see a current opening that aligns with their location, but want to be considered for future opportunities across our growing network of clinical research sites nationwide. We welcome interest from candidates who bring: A bachelor's or master's degree involving 1+ year of laboratory classes, preferably within a scientific or healthcare-related field (e.g., biology, chemistry, psychology, pre-med, or similar) and/or.
Director, Clinical Science BioNTech SEDirector, Clinical ScienceCambridge, MALead the design of clinical trials by developing study protocols, identifying patient populations, selecting endpoints, and determining optimal study designs to evaluate investigational drugs. You will collaborate across diverse teams to ensure the successful design and execution of clinical trials, directly contributing to our goal of improving patient outcomes worldwide.
Electronics Engineer, IS-855-13 Smithsonian Astrophysical ObservatoryElectronics Engineer, IS-855-13Cambridge, MA$119,355–$155,164 / yearSpecialized experience for this position would include significant experience in general electrical engineering, experience supporting architecting system level electrical designs using both commercial and custom electronics, and supporting project design reviews and participating in other projects’ reviews. Expert knowledge of the concepts, principles and practices of electrical engineering, in order to investigate, design, and provide consultative services to the development of a range of electronics for ground-based and space-borne instrumentation for astrophysical data collection, as well as its associated test, calibration and ground support equipment.
Medical Oncologist - Multiple Disease Site Options Tufts MedicineMedical Oncologist - Multiple Disease Site OptionsBoston, MA$255,670–$331,507 / yearThe successful candidate will play a central role in leading and growing our existing clinical trial infrastructure as well as the design, activation, and conduct of Phase I and first-in-human studies, contribute to the strategic growth of the Phase I program, and provide outstanding clinical care within a collaborative, mission-driven academic medical center. Tufts Medical Center in Boston, Massachusetts, is seeking a medical oncologist with focused experience in early-phase clinical trials to lead our Early Phase translational research efforts within the academic oncology program.
Biorepository Core Manager - Breast Oncology Dana-Farber Cancer Institute IncBiorepository Core Manager - Breast OncologyBOSTON, MA$77,600–$88,100 / yearManage freezer farm and critical equipment readiness: Oversee freezers and supporting laboratory equipment across sites, including maintenance/service coordination, calibration/maintenance documentation, relocations, sensor installation and monitoring coordination (e.g., with CAMS), review of temperature trends, and defined escalation/response processes for critical alarms, including after-hours coverage as needed. Oversee billing, budgeting, and recharge operations: Manage iLabs account setup and service workflows, develop/track quotes and purchase orders as applicable, consolidate and reconcile monthly charges, and coordinate submission of billing charges/journal entries with Research Administration; monitor operational expenses and implement mitigation actions as needed.
Research Data Specialist - Gastrointestinal Oncology Dana-Farber Cancer Institute IncResearch Data Specialist - Gastrointestinal OncologyBOSTON, MA$50,500–$56,700 / yearWe strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. The hiring range is based on market pay structures, with individual salaries determined by factors such as business needs, market conditions, internal equity, and based on the candidate's relevant experience, skills and qualifications.
Research Administrator Dana-Farber Cancer Institute IncResearch AdministratorBOSTON, MA$64,700–$71,700 / yearThe RA is responsible for liaising with Institute central offices such as Research Finance, Accounts Payable, Research Administration, Special Funds, Grants and Contracts, the Clinical Trials Office, Office of General Counsel, and the Innovations Office. The Research Administrator for the Department of Medical Oncology and the Divisions of Molecular and Cellular Oncology and Solid Tumors RA is responsible for the management of the research portfolio(s) for one or more laboratories (and Disease Centers, as applicable) with direction and moderate supervision from their supervisor.
Legal Counsel Rhythm PharmaceuticalsLegal CounselBoston, MA$200,000–$340,000 / yearResponsibilities and Duties Provide leadership and management for clinical trial contracting processes, day-to-day advice and review of contracts with Clinical Research Organizations (CROs) and other clinical trial vendors and clinical trial sites, liaising with senior leaders to manage and escalate issues and working cross-functionally and within the Legal & Compliance Department to ensure streamlined clinical trial contracts review and consistency in compliance with applicable policies and process for the Contract Lifecycle Management platform (CLM). Opportunity Overview Rhythm seeks an experienced and highly motivated mid-level (5-8 years) attorney with a strong life sciences background, experience providing legal support to clinical operations, and contract drafting and negotiation experience with the agreements and documentation required to support global clinical trials, to join its Legal & Compliance Department in its Boston office.
Medical Director, Clinical Development (Oncology), Cambridge, MA Isomorphic LabsMedical Director, Clinical Development (Oncology), Cambridge, MACambridge, MAAt IsoLabs, we are committed to leveraging state-of-the-art AI to advance precision medicine paradigms and establish new benchmarks for both efficacy and safety by consistently delivering the optimal treatments to the appropriate patients at precisely the right time, which we expect to significantly enhance our overall probability of success. By harnessing AI’s powerful capabilities, we can use it to model complex biological phenomena to help design novel molecules, anticipate how drug candidates will perform in the clinic and develop medicines to treat and cure some of the world’s most devastating diseases.
Executive Director / Vice President, Medical Affairs Relay TherapeuticsExecutive Director / Vice President, Medical AffairsCambridge, MAYou will lead the Medical Affairs function through this pivotal transition from late-stage development to commercialization readiness, partnering closely with internal and external stakeholders to develop solutions that drive awareness of Relay Therapeutics' genetic vascular anomaly portfolio, incorporate critical insights into medical strategy, and build external networks and partnerships to advance clinical trials, patient identification, and access to specialized care. Built on unparalleled insights into protein motion and how this dynamic behavior relates to protein function, we aim to effectively drug protein targets that have previously been intractable, with an initial focus on enhancing small molecule therapeutic discovery in targeted oncology.
New["Regulatory Coordinator - M Dougan Lab","Regulatory Coordinator - M Dougan Lab"] Dana-Farber Cancer Institute["Regulatory Coordinator - M Dougan Lab","Regulatory Coordinator - M Dougan Lab"]Boston$55,530–$61,700 / yearThis position will work collaboratively with a variety of personnel atall levels, including faculty and study team members of DF/HCC and external institutions, cooperative groups, clinical trials experts, representatives from the pharmaceutical industry, federal agencies, and other research organizations. The Regulatory Coordinators (RC) works under the direction of the Principal Investigator(s), Regulatory Operations Manager, Clinical Research Manager and / or directly for the Clinical Trials Office to complete the regulatory requirements of the clinical research project.
Clinical Trial Associate Verastem IncClinical Trial AssociateBoston, MA$86,000–$100,000 / yearCompany Profile: At Verastem Oncology, were advancing innovation and addressing the urgent needs of patients living with cancers driven by RAS/MAPK pathway mutations, a key driver of tumor growth and treatment resistance. The FDA approval of AVMAPKI FAKZYNJA CO-PACK delivered the first therapy specifically for women living with recurrent KRAS-mutated low-grade serous ovarian cancer, a rare cancer with significant unmet need.
Senior Clinical Development Scientist PhilipsSenior Clinical Development ScientistCambridge, MA$148,000–$237,000 / yearYou are the right fit if: You have acquired a minimum of 7+ years' clinical experience within FDA regulated medical device environments, with a focus on clinical research/development/real world evidence (RWE); strong scientific background and experience with Artificial Intelligence algorithm clinical performance validation. Collaborate with key internal and external stakeholders to provide in-depth expertise to develop and lead clinical initiatives through non-clinical and clinical strategies for new product development initiatives and product life cycle management.
Experienced Clinical Research Associate - Hematology/Oncology Medpace, Inc.Experienced Clinical Research Associate - Hematology/OncologyBoston, MassachusettsRemoteOn-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Research Data Specialist - Breast Oncology Clinical Trials Dana-Farber Cancer Institute IncResearch Data Specialist - Breast Oncology Clinical TrialsBOSTON, MARemote$50,500–$56,700 / yearWe strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. Develop knowledge of specialized data sources specific to outcomes data reporting, including routine reaching out to offsite providers to obtain information from medical records at outside sites of care.
NewRegulatory Coordinator - Center of Early Detection & Interceptions Blood Cancers Dana-Farber Cancer Institute IncRegulatory Coordinator - Center of Early Detection & Interceptions Blood CancersBOSTON, MARemote$55,530–$61,700 / yearThis position will work collaboratively with a variety of personnel at all levels, including faculty and study team members of DF/HCC and external institutions, cooperative groups, clinical trials experts, representatives from the pharmaceutical industry, federal agencies, and other research organizations. The Regulatory Coordinators (RC) works under the direction of the Principal Investigator(s), Regulatory Operations Manager, Clinical Research Manager and / or directly for the Clinical Trials Office to complete the regulatory requirements of the clinical research project.
NewResearch Data Specialist - GI Oncology Clinical Trials Dana-Farber Cancer Institute IncResearch Data Specialist - GI Oncology Clinical TrialsBOSTON, MARemote$50,500–$56,700 / yearThe GI Oncology Clinical Research Program supports PI initiated, industry sponsored, and cooperative group phase I - IV clinical trials across multiple GI cancers, including esophageal, stomach, liver, pancreas, colon, and neuroendocrine. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations.
NewRegulatory Coordinator - Sarcoma Clinical Trials Dana-Farber Cancer Institute IncRegulatory Coordinator - Sarcoma Clinical TrialsBROOKLINE, MARemote$55,530–$61,700 / yearThis position will work collaboratively with a variety of personnel at all levels, including faculty and study team members of DF/HCC and external institutions, cooperative groups, clinical trials experts, representatives from the pharmaceutical industry, federal agencies, and other research organizations. The Regulatory Coordinators (RC) works under the direction of the Principal Investigator(s), Regulatory Operations Manager, Clinical Research Manager and / or directly for the Clinical Trials Office to complete the regulatory requirements of the Sarcoma clinical research project.