April 30, 2026For U.S. Positions: While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above. If you received an email purporting to be from Leidos that asks for payment-related information or any other personal information (e.g., about you or your previous employer), and you are concerned about its legitimacy, please make us aware immediately by emailing us at LeidosCareersFraud@leidos.com.
May 29, 2026For U.S. Positions: While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above. If you received an email purporting to be from Leidos that asks for payment-related information or any other personal information (e.g., about you or your previous employer), and you are concerned about its legitimacy, please make us aware immediately by emailing us at LeidosCareersFraud@leidos.com.
li>Analyzes global trends to monitor and recommend rule sets for clients, revising low risk queues and scoring models appropriately, identifying breaches and addressing AML-related alerts, and ensuring client assets are protected through activities such as card reissuance. - Researches and analyzes global fraud and AML activities, reviewing low risk queues and communicating with clients to revise scoring models and establish new rules for cards in affected regions while ensuring minimal adverse effects on cardholders.
p> Determining compensation for this role (and others) at Vaco by Highspring depends upon a wide array of factors including but not limited to: - the individual’s skill sets, experience and training;
- licensure and certification requirements;
- office location and other geographic considerations;
- other business and organizational needs. Determining compensation for this role (and others) at Vaco/Highspring depends upon a wide array of factors including but not limited to the individual’s skill sets, experience and training, licensure and certifications, office location and other geographic considerations, as well as other business and organizational needs.
While an hourly range is posted for this position, an eventual hourly rate is determined by a comprehensive salary analysis which considers multiple factors including but not limited to: job-related knowledge, skills and qualifications, education and experience as compared to others in the organization doing substantially similar work, if applicable, and market and business considerations. As a Systems Engineer, working on the Encryptor Manager, you'll be a member of a cross functional team responsible for developing mission critical Cybersecurity Manager Applications for a rapidly growing product line.
Along with health and financial benefits, athenistas enjoy perks specific to each location, including commuter support, employee assistance programs, tuition assistance, employee resource groups, and collaborative workspaces — some offices even welcome dogs. We offer IT solutions and expert services that eliminate the daily hurdles preventing healthcare providers from focusing entirely on their patients — powered by our vision to create a thriving ecosystem that delivers accessible, high-quality, and sustainable healthcare for all.
Known for tackling complex clinical challenges, the company invests heavily in R&D, values engineering rigor, and fosters a hands‑on, collaborative culture where technical excellence is recognized and rewarded. As the Senior Mechanical Engineer, Product Development, you will lead the design and development of innovative electromechanical medical products used in high impact clinical applications.
Recommend equipment, new concepts and techniques to improve performance, simplify construction, reduce costs, correct design or material flaws, or comply with changes in codes or regulations. As the nation's largest producer of clean, carbon-free energy, Constellation is focused on our purpose: accelerating the transition to a carbon-free future.
Ensures compliance with all applicable federal, state, and local regulation including but not limited to: Fair Debt Collections Practices Act, 940 CMR 7.00: Debt Collection Regulations, MGL Chapter 194 An Act Preventing Unlawful and Unnecessary Foreclosures, UDAAP, RESPA, Flood Disaster Protection Act, Fair Credit Reporting, Regulation Z (Truth in Lending), Regulation B (CRA), Bank Secrecy Act, Regulation P (Privacy of Consumer Financial Information), Service Members Civil Relief Act of 2003. Essential Job Responsibilities The essential functions include, but are not limited to the following: · Performs collection activities on all residential and consumer loans serviced including participation and investor loans in adherence to all applicable federal, state, local regulations, investor guidelines, mortgage insurance guidelines, and servicing agreements.
p/>The purpose of this position is to develop new scientific knowledge, technologies and engineering solutions to problems in fire dynamics and material flammability, which can be used for the prevention or control of industrial property loss. Job Description:
Established nearly two centuries ago, FM is a leading mutual insurance company whose capital, scientific research capability and engineering expertise are solely dedicated to property risk management and the resilience of its policyholder-owners.
Oversight of PCR equipment (both RT-PCR and digital PCR), single-cell sequencing platform, Seahorse bioanalyzers, Tissue Lyser, microscope, spectrophotometers, ultrasonicator, Bioanalyzer, and Qiacube, including maintenance of equipment and scheduling routine preventive maintenance service, quality control, following SOP, and documentation. The primary responsibility of the Senior Research Assistant will be to assist the Joslin research division with implementation and processing of samples provided by Joslin investigators for transcriptomic, metabolic, and genetic analyses, within the framework of the Molecular Phenotyping and Genotyping Core Laboratory.
The Senior Research Coordinator works with Principal Investigator and other research staff to coordinate and execute the NIH-funded study entitled: The Impact of Biological Mechanisms of Aging on Response Variability to Resistance Training in Older Adults (BRIO). They assist with various aspects of study set-up, study participant visits, and assorted tasks during the active study, including randomization, outcome measures, and interventions, as well as data collection, management, and quality control.
Manus is seeking a Research Associate (RA) or Senior Research Associate (SRA) to support high-throughput screening (HTS) and laboratory automation workflows to identify engineered microbial strains with enhanced performance. Manus works across industries and value chains to accelerate the transition to BioAlternatives – better performing and more sustainable versions of complex molecules traditionally sourced from plants, animals, or fossil fuels.
While promoting a culture of safety, this position is responsible for wide range of research safety programs including; required safety inspections, reviewing construction and design plans, conducting risk assessments of research experiments, reviewing activities involving hazardous materials (biologicals, recombinant DNA, hazardous chemicals, toxic gases, controlled substances), developing emergency action plans, developing and delivering health & safety training, providing training and facilitating the shipping of biological materials and chemicals, conducting incident investigations, and facilitating regulatory. The salary of the finalist selected for this role will be set based on a variety of factors, including but not limited to departmental budgets, qualifications, experience, education, licenses, specialty, training and internal pay comparison.
While promoting a culture of safety, this position is responsible for wide range of research safety programs including; required safety inspections, reviewing construction and design plans, conducting risk assessments of research experiments, reviewing activities involving hazardous materials (biologicals, recombinant DNA, hazardous chemicals, toxic gases, controlled substances), developing emergency action plans, developing and delivering health & safety training, providing training and facilitating the shipping of biological materials and chemicals, conducting incident investigations, and facilitating regulatory. Certification designation in a health and safety or related discipline preferred (Certified Safety Professional, Certified Hazardous Materials Manager, Certified Environmental Manager, Certified Industrial Hygienist, et).
In addition, the Senior Research Operations Data Manager develops innovative strategies to leverage operational data, collaborates with research leadership to improve the reliability and accuracy of operational processes, ensures projects are appropriately tracked and billed, and supports grant-related data processes across the Health System. This includes: - Minimum of 2 years of experience planning and implementing solutions in healthcare, technology, financial systems, or clinical systems environments, including conducting research using administrative datasets and SQL programming.
Research Clinical Coordinator conducts patient recruitment, administers questionnaires, abstracts medical records, maintains patient databases, enters data into sponsor-specific electronic data capture forms, performs administrative tasks, assists in grant preparation, and participates with the research team in preparation of data and other reports. The hospital is also the primary teaching affiliate of the nationally ranked Boston University School of Medicine (BUSM) and a founding partner of Boston HealthNet an integrated health care delivery systems that includes many community health centers.
In collaboration with departmental leadership, they also participate in multi-year strategic planning and oversee the development, management, and monitoring of budgets for assigned portfolios, ensuring alignment of resources with program growth, compliance, and quality improvement priorities. They maintain deep working knowledge of all aspects of assigned clinical research trials and related processes in order to anticipate needs, troubleshoot complex operational and regulatory issues, and provide expert guidance to investigators and staff.
p>The position also leads and participates in quality improvement and data optimization initiatives, develops innovative/cost-effective strategies to leverage clinical data in support of institutional research goals, collaborates with faculty and hospital research leadership to improve the efficiency, reliability, and accuracy of clinical data processes, and ensures projects are appropriately tracked and billed. POSITION SUMMARY:
The Senior Data Manager, Clinical Research works collaboratively with clinical research leadership to develop high-quality research data sets and reports using the Clinical Data Warehouse (CDW), while supporting operational and scientific process improvements.
To accomplish this, we utilize our proprietary TRILLIUM and MACROPA platforms: TRILLIUM allows fine-tuning of radioligand pharmacokinetics thereby enhancing the therapeutic index, while MACROPA simplifies the manufacturing process for the alpha-emitting isotope, actinium-225. The actual base salary offered will depend on a variety of factors, including qualifications, work experience, skills, level of education attained, certifications or other professional licenses held, the location in which the applicant lives and/or from which they will be performing the job, and other job-related factors permitted by law.
Position Responsibilities: Perform Pre-award functions such as assisting Principal Investigators in completion of grant applications, including budget development, administrative sections, collecting materials from collaborators, and obtaining institutional review/approval. Work with investigators to develop annual research/clinical trial budgets; reconciles monthly expenses to budget; forecasts over/under expenditures and provides regular status reports to the Principal Investigator.
Roslindale, Massachusetts30+ days ago
ul>Perform Pre-award functions such as assisting Principal Investigators in completion of grant applications, including budget development, administrative sections, collecting materials from collaborators, and obtaining institutional review/approval. Work with investigators to develop annual research/clinical trial budgets; reconciles monthly expenses to budget; forecasts over/under expenditures and provides regular status reports to the Principal Investigator.
Carries out a broad range of technically advanced research activities and procedures; evaluates conclusions and has considerable latitude to modify or devise methods and techniques as necessary to achieve desired results; typically supervises technical and sometimes administrative elements of the research unit. Individuals working within the Seed Lab in vivo team collaborate closely with researchers and support staff within the Seed Lab and rely on trust, accountability and teamwork to ensure both scientific rigor and animal welfare.
Cambridge, MA30+ days ago
To serve as a key member of the fiscal research administration team, providing critical support to our researchers conducting groundbreaking research across a wide range of fields, including: • Plasma science • Plasma fusion • Physics • Data science • Engineering • Magnetics • Nuclear magnetic imaging • Cryogenics • Geothermal engineering. As a senior research administrator, you will serve as an advisor and primary point of contact on complex pre- and post-award sponsored program activities, and provide cradle to grave contract, grant, gift, and fund policy and financial management for faculty and principal investigators (PIs).
Cambridge, MA30+ days ago
Preferred Skills: • 5+ years as a Clinical Research Coordinator (CRC) working with cardiology trials or equivalent experience • General understanding of the evaluation and diagnosis of common cardiac disorders and diseases • Experience with CTMS systems - preferably RealTime, Clinical Conductor, or CRIO. You'll then work with your assigned sites to deliver customized training and day-to-day support that encourages research best practices, drives the adoption of IH services and products, and ensures our sites achieve their research goals.
The Ideal Candidate will have: MSc in Biochemistry, Structural Biology, Biophysics, Molecular Biology, Chemistry, or a related field and 0-2+ years of experience, or a BSc in Biochemistry, Structural Biology, Biophysics, Molecular Biology, Chemistry, or a related field with 2-4+ years of related experience. Who Will Love This Job: You're excited to learn fast and build deep expertise in CryoEM and structural biology-this role offers hands-on training with advanced instrumentation, real ownership of experiments, and the chance to grow your technical skillset alongside experienced scientists.
Equipped with extensive experience in program and system design and implementation; integration of research compliance requirements into operational workflows; formation and leadership of institutional committees and workplan initiatives; and career and cultural development, the Senior Manager, Special Projects, is adept in shifting priorities as needed, ready to take on a wide variety of institutional interests. o Recommend process and systems enhancement to Clinical Trial Office Director and collaborate with BClientHS research and non-research departments to implement changes within Client and BClientHS wide systems, including but not limited to, Epic enhancements and other affiliated system integrations.
Cambridge, MA30+ days ago
This role reports to the Head of Oncology Research and involves providing global strategic leadership, scientific expertise, and business acumen to drive the success of our nonclinical research programs as well as providing scientific expertise support for clinical programs. Purpose: Senior Research Lead in Oncology at Astellas is a strategic leader and key member of our scientific oncology research team, dedicated to the discovery and development of innovative therapeutic compounds for cancer treatment.
This role is critical in ensuring the success of clinical manufacturing processes for our cell therapy programs by leading technical investigations, resolving quality events, and driving continuous improvement in analytical development. Cross-Functional Communication and CAPA Implementation: Serve as a liaison between manufacturing, quality control, quality assurance, and analytical development teams to address and resolve quality events.
Through the Iterative Health Site Network - a premier network of 100+ clinical research sites across the US and Europe - we help expand and expedite access to novel therapeutics for patients in need. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.
Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and assist the Executive Director and/or Associate Vice President in ensuring that appropriate Corporate personnel are informed of the progress of studies of our company and competitors' drugs, and of internal and external expert opinion on scientific questions relevant to their areas of responsibility. The Senior Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within their area of expertise, in terms of new scientific findings, research methodologies.