Sr, SAS Programming Analyst Integrated Resources, IncSr, SAS Programming AnalystWoodcliff Lake, New JerseyContractorBS or MS in Computer Science or related field; 5-7 years of strong experience in programming with clinical trial data and developing programs, testing, and documentation; Strong SAS programming skills required in Windows and UNIX environment, with proficiency in SAS/Base, SAS Macros, SAS/Graph, SQL; Extensive experience of handling SDTM mapping, related data structures, and programming to create SDTM data sets; Extensive experience in SDTM validation using OpenCDisc. Strong problem-solving skills; Able to work independently and as a team player; Good organizational, time management, and project management skills; Capable of communicating technical concepts.
Clinical Data Manager Integrated Resources, IncClinical Data ManagerWoodcliff Lake, New JerseyFull timePerform DM activities for in-house and outsourced trials: protocol review, CRF development, database set up activities, data validation process (including manual data review of listings), SAE reconciliation, managing local laboratory and external labs and database lock. Bachelor degree or above in scientific or related field Minimum 5-7 years' experience in Data Management with experience in managing projects, project teams.
Clinical Supply Manager Integrated Resources, IncClinical Supply ManagerJersey City, New JerseyContractorA minimum of a Bachelor's Degree and 4 years of experience in clinical supplies or a related supply chain role (supply or demand planning) is required OR a minimum of 8 years of experience in clinical supplies or a related supply chain role is required. • A minimum of 2 years of experience in multi-disciplinary CSC or Pharma R&D areas (manufacturing, packaging & labeling, logistics, supply chain, clinical operations, pharma/bio research R&D, project management) is highly preferred.
Senior Clinical Data Manager Integrated Resources, IncSenior Clinical Data ManagerWoodcliff Lake, New JerseyFull timeCoordinates and conducts setup activities, such as CRF design for complex trials, database structure design, CRF annotation, project document creation and/or approval, data entry screen design and testing, validation check creation, testing and approval. • Perform DM activities for in-house and outsourced trials: protocol review, CRF development, database set up activities, data validation process (including manual data review of listings), SAE reconciliation, managing local laboratory and external labs and database lock.
Senior Clinical Study Manager Integrated Resources, IncSenior Clinical Study ManagerWoodcliff Lake, New JerseyFull timeCollaborate with other team members to coordinate the development and finalization of key study documents including protocols, case reports forms, informed consent documents, study management plans and final clinical study reports. Oversee Clinical Trial Coordinator for assigned project to ensure successful management of project(s), including development of the project plan, maintenance of trackers, and generation of metrics reports.
Administrative Assistant Integrated Resources, IncAdministrative AssistantHicksville, New YorkContractorRequires extensive software and Internet research skills, flexibility, excellent interpersonal skills, project coordination experience, and the ability to work well with all levels of internal management and staff, as well as outside clients and vendors. Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.
Project Assistant Integrated Resources, IncProject AssistantFlorham Park, New JerseyFull timeCandidate must have native-speaker level fluency in English Proven organization skills for project management Written Communication skills a must Familiarity with MS Office applications including MS Word, MS Outlook, basic MS Excel Project management tools (optional). A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.
NewOncology CRA-Sponsor side! JobotOncology CRA-Sponsor side!New York, NY$125,000–$140,000 / yearInformation collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from Jobot, and/or its agents and contracted partners.
NewDirector/Senior Director - Program Management - Medical Affairs ArgyllinfotechDirector/Senior Director - Program Management - Medical AffairsAvenel, NJRemoteTitle Director/Senior Director - Program Management - Medical Affairs Location Remote / Client-facing; NJ preferred About Saama Saama focuses on the specialized needs of pharmaceutical and biotechnology companies, delivering transformative business outcomes through AI, advanced analytics, deep life-sciences expertise, and collaborative solution development. Provide expertise across investigator-initiated trials, research collaborations, non-interventional studies, observational research, Phase IV studies, and related evidence-generation activities.
Manager, Systems and Prospect Research Human HireManager, Systems and Prospect ResearchNew York, NY$70,000–$80,000 / yearThe ideal candidate will have experience working with nonprofit advancement systems, donor databases, and research tools, with the ability to translate data into actionable insights that support fundraising strategy and donor engagement. Develop and maintain reports, dashboards, and analytics to support fundraising campaigns, donor portfolios, membership programs, and pipeline management.
Investment Research Analyst Credit & Equities Madison-DavisInvestment Research Analyst Credit & EquitiesNew York, NYIt's an ideal next step for a high-performing analyst coming out of investment banking, restructuring, or an investing seat who is ready to transition into or grow within a buy-side research function. This is a research analyst opportunity at a leading global asset management platform, supporting portfolio managers and senior analysts across credit and equities strategies.
Preclinical Principal Scientist, Research & Development Cresilon, Inc.Preclinical Principal Scientist, Research & DevelopmentBrooklyn, NY$130,000–$240,000The Preclinical Principal Scientist will serve as a key scientific contributor, subject matter expert (SME), and Project Manager in the execution of Cresilon’s Preclinical Research Operations, including but not limited to in-vivo study design (Safety and Efficacy/Functionality evaluations), Preclinical Research Management, Vendor Management, and Preclinical Regulatory Strategy. Work with Contract Research Organizations (CROs) to execute both Biocompatibility / Safety and Efficacy/Functionality research, including negotiating, drafting, and managing research contracts and agreements with pre-clinical trial sites.
NewSpec 3, Clinical Research MillenniumSoft IncSpec 3, Clinical ResearchFranklin Lakes, NJWorks with many different disciplines (manufacturing, marketing, quality, regulatory, etc.), materials, products and processes in the development of core clinical laboratory and outside the core clinical laboratory products and services. This position will also provide support to guide and implement innovation, product development, clinical testing, manufacturing, and post market surveillance via interfacing with R&D and GCD to insure successful and timely completion of projects.
Clinical Research Project Manager iMPact Business GroupClinical Research Project ManagerMahwah, NJLeading people who perform project management duties involving cross-functional teams focused on delivering internal products or administrative systems. Organizing project activities and interdepartmental meetings, ensuring communication facilitates the completion of the program or project on schedule and within budget constraints.
Clinical Research Scientist LancesoftClinical Research ScientistParsippany, NJ$107Excellent verbal and written communication skills and interpersonal skills are required to maintain working relationship with team members to ensure scientific integrity of clinical studies. Prepares study protocols, amendments, specific sections of study manuals and Investigator meeting notebooks, and other documents as needed with appropriate guidance and supervision.
Security Research Engineer PensarSecurity Research EngineerNew York, NY$120,000–$175,000In parallel, you'll drive original offensive and open source security research, and feed everything you learn in the field back into the product so Pensar keeps getting sharper as a pentesting platform. You'll be on the front lines of customer engagements — using our open source tool Apex to run pentests, curate and present findings, and stand up our platform inside customer environments.
Senior Clinical Research Associate - Cardiovascular Medical Device T45 LabsSenior Clinical Research Associate - Cardiovascular Medical DeviceNew York, NYRemoteThe Senior Clinical Research Associate (CRA) will own site activation, clinical study startup, site management, enrollment performance, and protocol execution across VahatiCor’s cardiovascular medical device clinical trials. This role serves as the primary operational partner to clinical sites, driving site readiness, investigator engagement, enrollment success, and consistent protocol execution throughout the study lifecycle.
Research Scientist I - C-BIN Nathan S. Kline InstituteResearch Scientist I - C-BINOrangeburg, NYFull timeD. in neuroscience, cognitive neuroscience, psychology, biomedical engineering, computer science, or a related field• Strong background in human memory research, cognitive neuroscience, or a closely related area demonstrated by track-record of publications• Demonstrated ability to independently develop and execute novel analysis approaches on complex datasets• Scientific programming experience (e.g., Python, MATLAB, R)• Strong written and oral communication skills• Demonstrated expertise in advanced fMRI analysis approaches, including but not limited to multivoxel pattern analysis, temporal dynamics, functional connectivity• Experience with Transcranial Magnetic Stimulation (TMS) or other noninvasive human brain stimulation methods• Familiarity with multimodal data integration approaches, EEG and/or physiological data collection and/or analysis• Experience mentoring junior researchersBackground Investigation/Justice Center Review Requirements: Prospective appointees will be: 1) Checked against the Staff Exclusion List (SEL) maintained by the Justice Center for the Protection of People with Special Needs. JOB DUTIES:- Work both independently and collaboratively, taking ownership of analysis projects while contributing to a team-oriented research environment- Contribute to the conceptual design and implementation of NIH-funded studies on awake memory consolidation- Oversee data quality monitoring and preprocessing of fMRI, physiology, and behavioral data- Develop and execute novel, advanced data analysis projects on prospective and existing datasets with collaborative input- Drive manuscript preparation and publication of research findings- Mentor Research Assistants on data collection protocols and analysis projects- Participate in lab meetings and contribute to the broader intellectual life of the research group- Present research findings at national and international conferencesJOB QUALIFICATIONS:Minimum Qualifications:Bachelor's degree and two years of professional research in an appropriate field or master's degree in an appropriate field may substitute for one year of the experience.
Marketing/Research Assistant Michael Page InternationalMarketing/Research AssistantNew York, New York$100,000–$130,000 / yearFull timeThe ideal candidate will have experience supporting capital raising, investor relations, marketing, or client service functions at a hedge fund, alternative asset manager, private credit manager, private equity firm, family office, or boutique investment manager. 2-5 years of experience supporting investor relations, fundraising, business development, marketing, client service, or research functions within an asset management or alternative investments environment.
Research Associate Integrated Resources, IncResearch AssociatePearl River, New YorkFull timeAnalyze immune responses to vaccine candidates using techniques that include (but not limited to) various tissue culture techniques, ELISA, & neutralization assays. • Incumbent will carry out specific laboratory experiments specific to the monitoring of humoral and/or cellular immune responses to various candidate vaccine antigens.