Clinical Data Analyst Integrated Resources, IncClinical Data AnalystJersey City, New JerseyFull timeSummary: Responsible for setting up clinical trials in the iDARTs application, an internally developed tool for medical review of clinical trial data based on TIBCO's Spotfire. At the trial level, perform the following activities: Analysis, design and data mapping of new trials for iDarts.
Project Manager Integrated Resources, IncProject ManagerSouth Plainfield, New JerseyFull timeResponsible for the success of the global drug development, manufacturing, clinical trials; coordinates the operational aspects of ongoing global clinical trials to ensure meeting all required timelines as well as adherence to budget, quality and performance expectations. • Serve as the primary study contact during trial conduct including, but not limited to, regular conferences calls and team meetings with appropriate functional areas, management and vendors as necessary.
Clinical Scientist Integrated Resources, IncClinical ScientistEdison, New JerseyFull timeA 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. Investigates the feasibility of applying a wide variety of scientific principles and concepts to potential inventions, products and problems.
Marketing Data Analyst Integrated Resources, IncMarketing Data AnalystStamford, ConnecticutContractorBroad and deep knowledge of business metrics/scorecards, campaign analysis, experimental design, segmentation solutions, modeling applications, media evaluation, forecasting & financial calculations (ROI customer valuation),, customer strategy development, etc. The candidate must have a nice blend of Strategy & Analytics within both the Digital and traditional CRM space (direct mail & email) and must be hands on with tools like SQL, R, SAS, Python for data mining and analysis.
Associate Director, Clinical Development Trial Lead (CDTL) Associate Director, Clinical Development Trial Lead (CDTL) MindlanceAssociate Director, Clinical Development Trial Lead (CDTL) Associate Director, Clinical Development Trial Lead (CDTL)Stamford, CT$104.63 / hourThe Associate Director, Clinical Development Trial Lead (CDTL) independently leads the cross-functional study team in the development and execution of complex clinical trials and is accountable both regionally and globally to deliver clinical milestones on trial(s) with quality, on time, and within scope and budget. Independently drive and influence local, regional and global, cross-functional study team throughout study implementation, execution and closure empowering them to meet the clinical trial deliverables, including proactive issue management, contingency planning and issue resolution.
Sr. Clinical Project Manager Integrated Resources, IncSr. Clinical Project ManagerSouth Plainfield, New JerseyContractorA 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. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
Business Analyst - Full time Integrated Resources, IncBusiness Analyst - Full timeParsippany-Troy Hills, New JerseyFull timeElicit requirements using interviews, document analysis, requirements workshops, storyboards, surveys, site visits, business process descriptions, use cases, scenarios, business analysis, competitive product analysis, task and workflow analysis, and/or viewpoints. • Analytical skills, to critically evaluate the information gathered from multiple sources, reconcile conflicts, decompose high-level information into details, abstract up from low-level information to a more general understanding, distinguish presented user requests from the underlying true needs, and distinguish solution ideas from requirements.
Business Operations Associate Integrated Resources, IncBusiness Operations AssociateFlorham Park, New JerseyContractorCoordinate the compilation, distribution and storage of all departmental legal agreements and related U.S.-routed documents utilizing Ariba contracts and update all (global) post-agreement records via tracking documents and POMS. • Maintain tracking system for all payments that flow though the U.S. • Obtain actual and prepare spending reports (after the close of each accounting periods as requested by manager for global group).
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.
Associate Director, Clinical Development Trial Lead Net2SourceAssociate Director, Clinical Development Trial LeadStamford, CT$104.63 / hourThe Associate Director, Clinical Development Trial Lead (CDTL) independently leads the cross-functional study team in the development and execution of complex clinical trials and is accountable both regionally and globally to deliver clinical milestones on trial(s) with quality, on time, and within scope and budget. Independently drive and influence local, regional and global, cross-functional study team throughout study implementation, execution and closure empowering them to meet the clinical trial deliverables, including proactive issue management, contingency planning and issue resolution.
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.
Manager, Clinical Contracts & Finance - III* MindlanceManager, Clinical Contracts & Finance - III*Parsippany, NJManages the contract negotiation process across the entire life cycle including RFI, vendor identification, RFP, vendor selection decision, contracting negotiation, performance monitoring, change orders, and ensures proper closeout of agreements to maximize contract value and achieve target savings. " Excellent communication skills and comfort level interacting with internal and external teams across all levels, including regular interface with stakeholders and leadership team members.
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.
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.
NewScientist 2, Research & Development eTeam Inc.Scientist 2, Research & DevelopmentSummit, NJ$39.34–$41 / hourWork closely with cross-functional teams, including R&D, quality assurance, and production, to streamline processes and enhance product development. Formulate and prepare batches of consumer health products according to established protocols and specifications.
Ad Sales Research Manager PhaxisAd Sales Research ManagerNew York, NY$60–$64 / hourWe provide insights to our clients about how their campaign performed across the purchase funnel (including perceptual KPIs like awareness and consideration as well as behavioral KPIs like site traffic or sales impact). We are a strategically orientated group that partners with agencies and clients to measure the effectiveness of advertiser campaigns and sponsorships across content, platforms and properties.