Associate Director Clinical PharmacologySenior Clinical Pharmacologist Oncology AbbVie IncAssociate Director Clinical PharmacologySenior Clinical Pharmacologist OncologyWaltham, MASenior Clinical Pharmacologist: PhD with 0 years of experience, or Pharm D with 2+ years of experience in a relevant field, Master's Degree or equivalent education and typically 8+ years of experience, Bachelor's Degree or equivalent education and typically 10+ years of experience; (*relevant field includes experience with PK, PBPK, PK-PD, Pharmacometrics or systems pharmacology, Drug metabolism/Transporters). PhD with typically 4+ years of experience or Pharm D with typically 6+ years of experience in a relevant field, Master's Degree or equivalent education and typically 12+ years of experience, Bachelor's Degree or equivalent education and typically 14+ years of experience;(*relevant field includes experience with PK, PBPK, PK-PD, Pharmacometrics or systems pharmacology, Drug metabolism/Transporters).
Clinical Trial Manager, Clinical Operations, Infectious Disease Moderna IncClinical Trial Manager, Clinical Operations, Infectious DiseaseCambridge, MA$109,200–$174,600 / 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. Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team.
NewClinical Scientist 2 or 3, Clinical Development Xenon PharmaceuticalsClinical Scientist 2 or 3, Clinical DevelopmentNeedham, MassachusettsThe clinical scientist will provide scientific leadership at the study level, contribute meaningfully to program strategy, and serve as a key partner to cross-functional teams to ensure that clinical development plans, study designs, and data packages are scientifically rigorous, operationally feasible, and aligned with evolving regulatory expectations. Our Total Rewards program includes base salary, target bonus, and stock options, as well as a full range of benefits including medical, dental, vision, short-& long-term disability, accidental death & dismemberment, and life insurance programs, Employee Assistance Program, travel insurance, and retirement savings programs with company matching contributions.
Clinical Outcome Assessment (COA) Lead SanofiClinical Outcome Assessment (COA) LeadCambridge, MA$148,500–$214,500 / yearExample research activities for the COA team include the development of a disease conceptual model; the selection of COA instruments to measure specific concepts of interest; the psychometric assessment of the measurement properties of a COA instruments; the development and validation of new COA instruments; the development of briefing books or dossiers for regulatory consideration of COAs. Minimum 3 years of relevant experience in COA in Pharma/CRO/Consultancy: ideally proven track record from scientific publications in core COA disciplines such as COA data analyses and/or creation or validation of new COAs and/or COA endpoint strategy implementation.
Associate Director, Research Biostatistics CSL Behring LLCAssociate Director, Research BiostatisticsWaltham, MAThe Associate Director, Research Biostatistics provides strategic and scientific statistical leadership across CSL Research programs and translational science initiatives, partnering with multidisciplinary teams to design studies, analyse complex research datasets, and generate decision-relevant evidence that supports project and portfolio progression. Lead and perform complex statistical analyses across preclinical, translational, biomarker, imaging, omics, and human research datasets using advanced methodologies such as Bayesian methods, causal inference, longitudinal modelling, and machine learning.
Postdoctoral Research Associate - Computer Science (multiple positions) UMass LowellPostdoctoral Research Associate - Computer Science (multiple positions)Lowell, MassachusettsGeneral Summary of Position: The successful candidate will lead and contribute to research that identifies risk factors and protective factors for a broad range of diseases and clinical outcomes using the National VA longitudinal EHR system. The Postdoctoral Research Associate will play a central role in translating complex EHR-derived data into clinically meaningful insights with direct relevance to Veteran health.
Sr. Research Associate, In Vivo Pharm ModernaTXSr. Research Associate, In Vivo PharmCambridge, MassachusettsWe 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 involves performing in vivo procedures with a high degree of proficiency, working in a fast-paced collaborative environment, and building technical depth in autoimmune and immunology-focused pharmacology models.
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.
Senior Research Budget Specialist - Cardiology Iterative Scopes IncSenior Research Budget Specialist - CardiologyCambridge, MAThe Senior Clinical Research Budgets Specialist is a seasoned, strategic partner to the sites within Iterative Health''s growing domestic and international network - taking ownership of the most complex, high-value clinical trial budget negotiations and contract payment terms across the portfolio. 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.
NewResearch Budget Specialist - Cardiology Iterative Scopes IncResearch Budget Specialist - CardiologyCambridge, MAThe Clinical Research Budgets Specialist is a critical operational partner to the sites within Iterative Health''s growing domestic and international network - owning the development, review, and negotiation of clinical trial budgets and contract payment terms on their behalf. 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.
Postdoctoral Research Associate - Computer Science (multiple positions) University of MassachusettsPostdoctoral Research Associate - Computer Science (multiple positions)Lowell, MAGeneral Summary of Position: The successful candidate will lead and contribute to research that identifies risk factors and protective factors for a broad range of diseases and clinical outcomes using the National VA longitudinal EHR system. The Postdoctoral Research Associate will play a central role in translating complex EHR-derived data into clinically meaningful insights with direct relevance to Veteran health.
Sr. Research Associate, In Vivo Pharm Moderna IncSr. Research Associate, In Vivo PharmCambridge, 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 involves performing in vivo procedures with a high degree of proficiency, working in a fast-paced collaborative environment, and building technical depth in autoimmune and immunology-focused pharmacology models.
Research Associate I Charles River Laboratories International IncResearch Associate IWatertown, MA$29–$32 / hourIf you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
Clinical Trial Associate Candel TherapeuticsClinical Trial AssociateNeedham, MA$88,000–$100,000 / yearThis role includes working on multiple protocols with the potential to cross-train across different oncology indications using a variety of clinical trial databases. Our Science: Advancing Cancer Immunotherapies Candel is a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies that stimulate personalized, systemic anti-tumor responses.
Associate Director, Clinical Supplies Project Manager ModernaTXAssociate Director, Clinical Supplies Project ManagerCambridge, MassachusettsWe 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 scope includes the operational planning and strategy required to execute end-to-end supply management, including demand planning, label development, packaging/labeling, distribution, IRT UAT/supply management, temperature excursions, and site activations.
Director, Clinical Operations, Oncology 3316 Takeda Development Center AmericasDirector, Clinical Operations, OncologyMassachusettsOversight of Strategic Partners/CRO/vendor selection, budget and contract negotiation, and proper supervision of performance for all activities assigned to a Strategic Partner/CRO/vendor for assigned program(s), including escalation of issues to and participation in governance committees; accountable for operational risk management strategy in collaboration with Strategic Partners. The 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.
Clinical Contracts Manager, Cambridge, MA Isomorphic Labs LimitedClinical Contracts Manager, Cambridge, MACambridge, MAOperating at an organizational level, this role drives vendor selection, supports negotiation of Master Service Agreements (MSAs) and Clinical Trial Agreements (CTAs), and manages vendor related study budgets and contract lifecycle activities. 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.
R&D Domain Specialist – Research Technology & Innovation Associate Consultant (Discovery) ZSR&D Domain Specialist – Research Technology & Innovation Associate Consultant (Discovery)Boston, Massachusettsnbsp: As a R &D Domain Specialist – Research Technology & Innovation Associate Consultant in Discovery , you will apply your pharma R&D domain knowledge, consulting skills, and research technology experience to help clients improve and streamline drug discovery workflows at leading biotech and biopharma organizations. Bachelor’s degree required ; Master’s degree strongly preferred, ideally in Life Sciences, Business Administration, Health Informatics, Business Analytics, Computer Science, MIS, or a related field ; PhD in a pharma-relevant domain is a plus.
Research Associate II In Vivo Pharmacology MEDICILON USA CORPResearch Associate II In Vivo PharmacologyLexington, MAFull timeThe successful candidate will have hands-on experience conducting rodent studies in a CRO, biotechnology, or pharmaceutical environment and will be responsible for study execution, animal procedures, sample collection, and data documentation. This position works closely with study scientists and project teams to ensure high-quality study conduct, adherence to timelines, and compliance with animal welfare and regulatory requirements.
Research Associate, AD/QC - Fluidic Properties Terrestrial Bio IncResearch Associate, AD/QC - Fluidic PropertiesWoburn, MA$60,000–$75,000 / yearIn this role, you will execute routine and non-routine fluidic property testing such as viscosity, surface tension, UV-Vis spectrophotometry, and pH measurements to support formulation development, process characterization, and Quality Control (QC) release for our microneedle array patch (MAP) programs. Demonstrated hands-on experience operating laboratory instrumentation for viscosity (micro-viscometer or rotational viscometer), surface tension/contact angle measurement, UV-Vis spectrophotometry, and pH meters.