2027 Future Talent Program - Discovery Sample Management Automation - Intern Merck & Co Inc2027 Future Talent Program - Discovery Sample Management Automation - InternRahway, NJRequired Skills: Assay Development, Assay Development, Clinical Research, Cloud Data Catalog, Data Analysis, Database Management, Data Science, Data Security, Data Visualization, Data Wrangling, Detail-Oriented, Drug Discovery Process, ETL Pipelines, Event Planning, Immunochemistry, Key Performance Indicators (KPI), Laboratory Automation, Laboratory Equipment Calibration, Laboratory Informatics, Laboratory Information Management System (LIMS), Microsoft Visual Basic, Programming Languages, Project Management, Python (Programming Language), Scientific Research {+ 2 more}. Depending on the type of projects in which the lab is engaged at the time of the internship, activities that the intern may have the opportunity to undertake include, but are not limited to: Interface with our Research & Development Division's scientific staff to understand scientific workflows and associated automated systems.
NP/PA Critical Care Per Diem Weekends Hackensack Meridian HealthNP/PA Critical Care Per Diem WeekendsHackensack, New JerseyPer diemOverview: The Acute Care Advanced Practice Nurse (APN) or Physician Assistant utilizes a patient-centered coordinated care model, demonstrating competencies in leadership, direct clinical practice, consultation/collaboration, coaching/guiding, research, and ethical decision-making. The posted rate of pay in this job posting is a reasonable good faith estimate of the minimum base pay for this role at the time of posting in accordance with the New Jersey Pay Transparency Act and does not reflect the full value of our market-competitive total rewards package.
2027 Future Talent Program - Research Initiation & Budget Execution - Intern Merck & Co Inc2027 Future Talent Program - Research Initiation & Budget Execution - InternRahway, NJ$39,908–$111,111 / yearAI & Digital Tool Enablement: Partner with team members to pilot, test, evaluate, or enhance innovative AI-enhanced tools and specialized platforms (e.g., the Non-Interventional Research (NIR) Vendor Grading Tool) aimed at automating manual tasks, tracking deliverables, or streamlining literature reviews. The internship lasts up to 12 weeks and will focus on multiple projects centered around process improvement, workflow optimization, and the integration or evaluation of AI-enhanced tools (such as specialized non-interventional research platforms, automated budget management applications, or literature-screening AI tools).
2027 Future Talent Program - Clinical and Regulatory Strategic Communications - Intern Merck & Co Inc2027 Future Talent Program - Clinical and Regulatory Strategic Communications - InternRahway, NJ$39,908–$111,111 / yearClinical Regulatory & Strategic Communications (CRSC) is a multidisciplinary organization that plays a critical role in supporting the development of new medicines by creating key clinical and regulatory documents, communicating clinical trial results, and ensuring information is shared responsibly and transparently with regulatory agencies, healthcare professionals, trial participants, and the public. Seeking a highly motivated individual who is pursuing an education in the life sciences, medicine, pharmacology/pharmacy, quality, operations, data science, or a related field, and who is interested in writing, communicating about medicine and science, and supporting the quality, compliance and operational excellence activities that enable clinical research.
Associate Director, Strategic Engagements Ferring Pharmaceuticals IncAssociate Director, Strategic EngagementsNew York, NY$178,000–$218,000 / yearThis individual will serve as a commercial liaison to key urology and uro-oncology opinion leaders cultivating relationships with influential healthcare professionals, health system leaders, and operational stakeholders to generate actionable market insights, identify opportunities to improve patient access and adoption, and inform commercial strategy. Working in close partnership with Marketing, Medical Affairs, Market Access, Sales, Leadership, and Strategic Engagement colleagues, this individual will drive initiatives that strengthen community engagement, enhance stakeholder collaboration, and accelerate adoption of the brand across priority account settings.
Medical Operations Manager - NA PhotocureMedical Operations Manager - NAPrinceton, NJRemote$180,000–$210,000 / yearThis hybrid role includes operational oversite of projects in clinical development as well as post-approval studies at Photocure, in particular, the U.S. Cysview Blue Light Cystoscopy Registry, a large multi-center study collecting Real-World Evidence (RWE) from bladder cancer patients undergoing treatment. Specific Responsibilities and Activities include: Act as the primary point of contact for operational stewardship and oversight of the research projects including sponsored studies, the U.S. Cysview Registry and IITs (Investigator Initiated Trials).
Senior Consultant - Clinical Documentation Specialist DeloitteSenior Consultant - Clinical Documentation SpecialistNew York, NY$95,600–$188,400 / yearOther skills include the ability to analyze, act and design action plans upon monthly and quarterly reports related to individual providers, facilities, MS-DRGs, APR, PSIs, severity of illness and risk of mortality, capture rates, quality metrics and can effectively prioritize their work activities. Clinical Payments Optimization: Assisting clients by validating that payments for clinical healthcare services comply with regulatory, clinical based evidence and contractual requirements while also determining that payments are appropriate for the type and level of care provided.
Sales Enablement and RFI Manager Everest Clinical ResearchSales Enablement and RFI ManagerNew JerseyAs a Sales Enablement and RFI Manager, you are a key member of the Commercial Services/Proposals team; developing, writing, and finalizing responses to client and prospect Requests for Information (RFIs) and similar documents such as capabilities presentations in PowerPoint. Supports preparation of proposal documents and bid defense slide decks using templates provided, including drafting PowerPoint slides to summarize therapeutic area experience (tables, charts, slide text), team profiles, and other summary content where needed.
NewSenior Statistical Project Leader SanofiSenior Statistical Project LeaderMorristown, NJ$178,500–$257,833.33 / yearAbout the Job: Our Evidence Generation and Decision Science (EGDS) group at Sanofi unites Biostatistics, Clinical Statistical Modeling, and Real-World Evidence to revolutionize data-driven decision making through cutting-edge quantitative science and deliver unparalleled integrated evidence that drives innovation and scientific breakthroughs. Provide advanced level of statistical and scientific contributions to clinical development plans, protocol, SAP, CSR, regulatory documents, studies and submissions activities (when applicable), and provide strategic statistical leadership for responsible projects in Sanofi's solid tumor pipeline.
Clinical Specialist (PT, OT, or SLP) - Brooklyn NYU Langone HealthClinical Specialist (PT, OT, or SLP) - BrooklynBrooklyn, NY$82,886.36–$126,000Full timeRequired Licenses: Speech Pathologist Lic-NYS, Phys Thrpst License-NYS, Occup Thrpst License-NYS, ASHA Cert. Additionally, all employees have access to our holistic employee wellness program, which focuses on seven key areas of well-being: physical, mental, nutritional, sleep, social, financial, and preventive care.
Director of Clinical Science - Hematology SystimmuneDirector of Clinical Science - HematologyPrinceton, NJFull timeAuthor components with the Medical Director and reviewer of clinical and regulatory documents and registration dossiers (i.e., protocol, ICF, IB, safety updates, study reports, regulatory submissions, etc.) to support registration and commercialization of the compound(s). SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development.
Associate Director, Project Management - Value & Implementation (VIPM) (Hybrid) Merck & Co IncAssociate Director, Project Management - Value & Implementation (VIPM) (Hybrid)Rahway, NJ$142,400–$224,100 / yearPosition Description/Summary: The GPAM Associate Director, Value & Implementation Project Manager (VIPM), is a core member of Value & Implementation (V&I) Team, partnering with team leaders to develop strategies and execute our Company's drug and vaccine V&I efforts to progress the R&D pipeline and realize its full potential. This includes integrating strategic and tactical input from disciplines (e.g., Medical Affairs, Outcomes Research, Market Access, Biostatistics and Research Decision Sciences, Commercial, and other areas) as applicable to the project.
2027 Future Talent Program - Global Clinical Trial Operations Intern Merck & Co Inc2027 Future Talent Program - Global Clinical Trial Operations InternRahway, NJ$39,908–$111,111 / yearThe intern will engage with GCTO Regions and Regional Operations leadership team and general staffing team members for participation in and/or leading projects that support regional operations driving the efficient and ethical conduct of clinical trials across the region. The Regional organization is comprised of 5 distinct regions (North America, Latin America, Asia Pacific, European Economic Area and Non-EU/Middle East/Africa) and is responsible for a significant proportion of the GCTO budget, staff and deliverables.
2027 Future Talent Program - Global Clinical Data Standards - Intern Merck & Co Inc2027 Future Talent Program - Global Clinical Data Standards - InternRahway, NJ$39,908–$111,111 / yearMerck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. We are looking for an intern to help us drive adoption of emerging processes, tool and technologies in information management through collaboration with our internal stakeholders.
Business Development (Clinical Services) Theradex OncologyBusiness Development (Clinical Services)Princeton, New Jersey$175,000–$225,000 / yearFull timeResponsible for maintaining both paper and electronic files including all proposals, and fully executed copies of all Master Service Agreements, Work Orders, Consulting Agreements, Letters of Intent. The company was founded in 1982 working with the National Cancer Institute, which led to its expansion to working with industry sponsors developing cancer therapeutics.
Clinical Study Specialist ICON PlcClinical Study SpecialistWarren, NJ$62,376–$77,970 / yearCompiles study manuals including but not limited to: study reference binders and manuals and maintains versioning of study reference materials (e.g., regulatory, pharmacy, and laboratory binders. Tracks and monitors close out activities - study close-out documents (1572s, Investigational Product reconciliation, Financial Disclosures, etc.) and CRA close-out visits.
Clinical Support Specialist ICON PlcClinical Support SpecialistWarren, NJ$62,376–$77,970 / yearCompiles study manuals including but not limited to: study reference binders and manuals and maintains versioning of study reference materials (e.g., regulatory, pharmacy, and laboratory binders. Tracks and monitors close out activities - study close-out documents (1572s, Investigational Product reconciliation, Financial Disclosures, etc.) and CRA close-out visits.
NewClinical Sales Account Manager H1 InsightsClinical Sales Account ManagerNY$115,000–$140,000 / yearBuild trusted, consultative relationships with mid-level stakeholders across Clinical Operations, Site Selection, Feasibility, Patient Recruitment, and Regulatory functions, serving as a knowledgeable and reliable point of contact throughout the customer lifecycle. Deeply embedded in your client's organization, you will understand the pressures of trial timelines and site performance, position solutions that address their evolving needs, and help them unlock the full value of H1's data solutions and AI-powered Clinical solutions.
Contractor, Clinical Operations PTC TherapeuticsContractor, Clinical OperationsWarren, NJ$60–$80 / hourPrimary duties/responsibilities: Performs as an integrated member of the clinical team to lead, direct and contribute to, the planning, execution, and reporting of clinical trials, including estimation of clinical project timelines, protocol writing, Case Report Form (CRF) design, site selection, study drug forecasting, site and Clinical Research Organization (CRO) management, data review, and study reporting; recommends monitoring, safety, eligibility, enrollment, and data consistency strategies. Manages clinical study timelines using the appropriate project management tools; develops budgets and manages expenditures for clinical trial program, including those for investigational sites and vendors; presents project progress reports through accurate, succinct summaries of clinical study work at internal team meetings and investigator meetings.
Associate Director, GRACS BD Merck & Co IncAssociate Director, GRACS BDRahway, NJ$129,000–$203,100 / yearRecruits and onboards due diligence team members to the due diligence project, facilitates discussions with GRACS due diligence team members to identify gaps and risks, tracks progress and coordinates GRACS due diligence summary reports, ensures GRACS Leadership is made aware of critical due diligence findings as needed, and liaises with GRACS Portfolio and Prioritization group to support GRACS resource estimation. Charter and manage deal-specific GRACS implementation teams comprised of representatives from the impacted functions/ processes; responsibility will include (a) utilizing project management tools to drive development of implementation project plans; (b) identifying & ensuring cross-functional alignment of interdependent activities; and (c) driving execution of the plans through to project close-out.