Account Manager (Life Sciences) Cynet CorpAccount Manager (Life Sciences)Philadelphia, PARemoteWorking within a vibrant, high-velocity team, you will bring your operational energy and strategic expertise to manage, farm, and scale major existing national and regional enterprise accounts within the Life Sciences, IT, and Engineering MSP, VMS, and SOW spaces. Serving as the primary link between clients, MSP partners, and delivery teams, this role oversees contingent workforce programs, staff augmentation engagements, SOW-based projects, and enterprise-scale MSP delivery.
Construction Supervisor Integrated Resources, IncConstruction SupervisorSouth Plainfield, New JerseyContractorReview Wiring, Control and Schematic drawings for accuracy, coordinate and perform testing and commissioning of equipment and facilities, including necessary relay / controls tie-ins. Perform electrical construction supervisory responsibilities for the Inside Plant Construction Group in the Delivery Projects and Construction (DP&C) Organization.
Sr. Manufacturing Technician Integrated Resources, IncSr. Manufacturing TechnicianSouth Plainfield, New JerseyContractorThe Manufacturing Technician performs or leads functions associated with Manufacturing operations, including set-up and calibration tasks, aseptic processing and sampling operations, single-use component set up and operations, buffer formulation and transfer, TFF, depth filtration, polishing and sterile grade filtration, viral removal operations, column chromatography, and final fill operations. Writes routine reports, quality documents ( SOPs, batch records, deviations, change controls ), and shift exchange summaries.
Indirect Sales Representative Integrated Resources, IncIndirect Sales RepresentativeKearny, New JerseyContractorChannel Growth: Direct local contract negotiation and start-up implementation of new accounts, as well as new distribution marketing, advertising, and sales strategies for new and existing accounts. Meet and exceed regional sales objectives through the management and implementation of all sales, marketing, merchandising, and advertising/promotional programs.
Director of Financial Auditing/Compliance Slipstream ITDirector of Financial Auditing/ComplianceHampton, NJThe Director of Financial Auditing/Compliance leads the organization's internal audit and Sarbanes-Oxley (SOX) compliance program, ensuring the integrity of financial reporting, the effectiveness of internal controls over financial reporting (ICFR), and adherence to regulatory requirements across a complex, GxP-regulated life sciences environment. The ideal candidate combines deep SOX/ICFR technical expertise with life sciences industry fluency (GxP, clinical trial cost accounting, revenue recognition for licensing/royalty arrangements, and R&D capitalization) and the executive presence to partner directly with the CFO, external auditors, and the Board.
Medical Writer Integrated Resources, IncMedical WriterMadison, New JerseyContractorThe author will contribute essential deliverables which could include clinical overviews, integrated analyses of safety and efficacy, responses to regulatory questions, risk management plans, REMS, key sections of the Investigator's Brochure, the Annual Safety Report and regulatory briefing documents. Individual will create and foster an environment of partnership with other members of product teams, in collaboration with the Project Team, assess document requirements, complexity, and potential issues with a submission, and develop strategies to deal with these, and lead a team of internal and external (contractors) authors.
ARIBA SOURCE TO PAY SPECIALIST Integrated Resources, IncARIBA SOURCE TO PAY SPECIALISTPrinceton, New JerseyContractorCreate and submit User Access Review (UAR) files based upon the respective system schedule; keeping knowledge base current on S2P technology user access rights; manage the administration of access provision within S2P technology, including management of eSetup escalation and issue resolution, and support through software releases. Assist manager with S2P technology and automation projects including: develop, document, and execute test scripts, document results of test scripts, investigate root cause of testing defects, and provide updates on deliverable status.
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.
VIRTUALIZATION AND SERVER ADMIN Integrated Resources, IncVIRTUALIZATION AND SERVER ADMINBridgewater, New JerseyFull timeManage and administer Server Virtualization (VMware 4.x & 5.x/Citrix 5.x) and Windows Servers: • Build/design VM Requirements, manage and perform physical server host and guest operating system maintenance, installation, patching, configuration, support, backup/restore, monitoring, trending. The Virtualization and Server Administrator is responsible for advanced administration, design, build, implementation and support of server environments, including VMware vSphere-hosted virtual machines, Citrix XenApp farms, and physical Windows servers.
Manufacturing Technician Integrated Resources, IncManufacturing TechnicianSouth Plainfield, New JerseyFull timeManufacturing Technician performs functions associated with all manufacturing operations, including set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components, subassemblies and final assemblies. While performing the duties of this job, the employee is frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms; and talk or hear.
Senior Director Quant Pharm Penfield Search PartnersSenior Director Quant PharmPrinceton, NJThe Quantitative Pharmacology group is responsible for the oversight over drug development aspects related to clinical pharmacology and pharmacometrics of clinical development candidates, working in close collaboration with nonclinical and clinical functional areas. Development and execution of model-based analyses including translational PK/PD approaches, population pharmacokinetic models, exposure-response models, clinical trial design simulations, and quantitative systems pharmacology (QSP) modeling.
IT Pharma Project Manager Consultant - biopharmaceutical Shiftcode Analytics, IncIT Pharma Project Manager Consultant - biopharmaceuticalPrinceton, NJThis role bridges the gap between scientific teams, IT, and business functions to ensure that digital infrastructure, data systems, and enterprise applications are implemented effectively, securely, and on time. The IT Project Manager will oversee the planning, execution, and delivery of technology initiatives that support the company's biotechnology research, development, and operations.
IT Manager Position Integrated Resources, IncIT Manager PositionNewark, New JerseyFull timeAccountable for maintaining effective internal controls over the processes and transactions under areas of responsibility including the completeness and accuracy of financial information and transactions, compliance with applicable laws and regulations, and the effectiveness and efficiency of operations. The individual assigns work, develops and maintains project plan, performs resource management, develops time and cost estimates, monitors budget for area of responsibility and performs HR activities for team members.
Regulatory Project Manager II Integrated Resources, IncRegulatory Project Manager IIRaritan, New JerseyFull timeResponsibilities will include: active follow-up on the progression of all regulatory activities required for successful and timely completion of the regulatory deliverables, monitoring regulatory driven key milestones, decision points and critical path activities, creation of project related reports to support decision making at the PMT, GRT and CDT level, regulatory portfolio oversight, support of team member planning of short and long term deliverables and informing stakeholders on project deliverables status. The incumbent will work in close collaboration with the GRL to proactively prepare regulatory activities to be discussed in the GRT and will also work in close collaboration with the Regulatory Liaisons and Scientists to work out NA-EMEA-APJLA specific details on Health Authority interactions and submissions.
Trial Supply Manager Integrated Resources, IncTrial Supply ManagerPennington, New JerseyContractorA 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. A minimum of a Bachelors 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.
Senior Epic Project Manager Cardiac Partners Consulting, Inc.Senior Epic Project Manager CardiacPhiladelphia, PARemoteOur direct client is seeking an experienced Senior Epic Project Manager to lead a high-profile Cardiac Refuel Program, a strategic optimization initiative focused on improving clinical, operational, financial, scheduling, registration, and patient access workflows across the Cardiac service line. Drive decision-making, issue resolution, and change management activities including Epic Cardiac Optimization initiatives such as: Patient Access & Scheduling Transformation and Clinical Workflow Optimization (CPRU Infusion workflows).
Global Trial Manager-III Integrated Resources, IncGlobal Trial Manager-IIIHorsham, PennsylvaniaContractorContacts inside the company: • Clinical Program Leaders, Clinical Operations Heads, Other Global Trial Managers, R&D Country Directors, R&D Country Managers, Clinical Pharmacology Project Managers, Clinical Research Managers, Local trial Managers, Site Managers, Clinical trial Assistants, Pharmacokinetic Research Managers, Finance, Central Business Operations, IDAR, IDMs, Quality Management & Training group, Quality Assurance group, and different members of the Medical Affairs Team and the Clinical Team. This position leads the Study Management Team (SMT) and interfaces with the correspondent Clinical Teams, other Global Clinical Development Operations (GCDO) functions, Regional Trial Coordination/Site Management (TCSM) colleagues, Study Sites (if applicable), Central Business Operations, finance and the corresponding medical affairs team/Operating Company.
Clinical EMR Configuration Analyst NTT DATAClinical EMR Configuration AnalystPrinceton, NJRemote$52.50–$75 / hourThe ideal candidate brings strong analytical and consulting skills, stakeholder management capabilities, excellent communication, and the ability to think critically in fast-paced Agile environments while delivering measurable business value. We are seeking a Clinical EMR Configuration Analyst with strong clinical systems experience to support EMR configuration, QA, conversion workflows, and healthcare transformation initiatives, with a focus on WellSky implementations.
NewClinical Director / BCBA ICBDClinical Director / BCBALanghorne, PA$125,000–$150,000Dedication to Better Outcomes – Smaller caseloads combined with our established clinical infrastructure mean we can focus on delivering high-quality care and lasting impact for children and families. Investment in Talent – We hire top talent and invest in developing our RBT teams, ensuring the best care for our clients and stability for our BCBAs.
CT Clinical Applications Specialist PEAK Technical StaffingCT Clinical Applications SpecialistPrinceton, NJCandidate Privacy To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to https://peaktechnical.com/privacy-policy/and https://peaktechnical.com/ca-residents-privacy-rights/ Become a recognized expert in product and clinical technical competencies, analyzing and resolving issues concerning clinical applications and product software.