Senior Clinical Lead, Early Clinical & Experimental Therapeutics SanofiSenior Clinical Lead, Early Clinical & Experimental TherapeuticsMorristown, NJ$236,250–$393,750 / yearIn these roles, duties include: Design safe, rapid and informative First-In-Human studies for oncology assets potentially including natural history, experimental model validation, mechanistic and signal seeking, streamlined Proof-of-Mechanism as well as Proof-of-Concept studies providing robust data for early Go/No Go decisions and other pharmacokinetic studies. A key focus of this role is to support the path from the research phase through early clinical development including early and rapid Proof-of-Mechanism/Proof-of-Concept, as well as natural history studies and experimental model validation to contribute to Human Target Validation (HTV) and evaluating the pharmacology of novel therapeutic approaches.
Senior Statistical Programmer (Remote) Everest Clinical ResearchSenior Statistical Programmer (Remote)New JerseyRemoteTo drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Senior Statistical Programmer for our Bridgewater, New Jersey, USA on-site location, or remotely from a home-based office anywhere in the USA in accordance with our Work from Home policy. Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries.
Sr. Business Analyst St. Jude Children's Research Hospital IncSr. Business AnalystNYRemote$86,320–$154,960 / yearThroughout the institution, across the clinical, research, administrative, and operational domains there are many clinical research customers who need access to accurate and consistently defined data to drive insightful analytics and support the broader research mission of the organization. This is an estimate offered in good faith and a specific salary offer takes into account factors that are considered in making compensation decisions including but not limited to skill sets, experience and training, licensure and certifications, and other business and organizational needs.
Senior Director of Clinical Science - Hematology Merck & Co IncSenior Director of Clinical Science - HematologyRahway, NJ$190,800–$300,300 / yearThe Senior Director partners closely with Section Heads, Asset Leads, Program Development Team Leads, and cross-functional development team members to support study planning, data interpretation, issue resolution, and broader program decisions across assigned studies and programs. Required Skills: Change Agility, Clinical Development, Clinical Oncology, Clinical Reporting, Clinical Research, Clinical Sciences, Clinical Study Management, Clinical Trial Management, Hematology, Medical Sciences, Oncology, People Leadership, Scientific Literacy.
Senior Director Clinical Development, Breast Cancer BeOne Medicines AGSenior Director Clinical Development, Breast CancerNY$299,800–$369,800 / yearThe Senior Director, Clinical Development, Solid Tumors will support BeOne Clinical and Medical assets by successful execution of clinical development programs and deliverables in partnership across the organization; with external vendors; and with external academicians and collaboration partners. Previous participation in a clinical development program is essential, including involvement in all stages of clinical trials (i.e. from start up to study report), ideally having taken at least one study through from start to finish in a clinical scientist role.
Senior Clinical Drug Supply Manager Amneal Pharmaceuticals IncSenior Clinical Drug Supply ManagerBridgewater, NJ$170,000–$190,000 / yearEssential Functions: Clinical Supply Planning & Execution: Develop and maintain demand forecasts based on study protocols, enrollment assumptions, and country/site activation plans; Support development and maintenance of study supply plans and timelines for all studies (e.g., Oncology, Parkinson's Disease studies); Lead in planning supply strategies for multiple global complex trials (e.g., dose escalation cohorts, randomized arms, combination therapies); Track randomization, study enrollment, drug supply management and adjust supply forecasts to ensure alignment with study needs, utilizing external Interactive Response Technology (IRT) system; Coordinate global supply activities including inventory and storage management, depot stocking, re-supply strategies, expiration management, IMP destruction, IMP shipping conditions across multiple clinical studies and regions to ensure uninterrupted drug availability at sites. Study Team Partnership - Vendor & Stakeholder Management: Serve as a point of contact for external vendors including Clinical Research Organizations (CROs), packaging providers, depots and the Clinical Study Drug Coordinator on cross-functional study teams; Collaborate with Clinical Operations and site personnel to address supply-related inquiries and ensure site readiness; Support vendor oversight activities, including performance tracking and issue escalation; Communicate with cross-functional teams including Clinical Operations, Regulatory Affairs, and Quality Assurance; Collaborate closely with Clinical Operations to align supply strategies with study design, enrollment, and timelines; Provide input into protocol design (e.g., dosing schedules, packaging configurations, blinding strategies) to ensure supply efficiency.
Senior Director, Clinical Development PTC Therapeutics IncSenior Director, Clinical DevelopmentWarren, NJ$289,200–$364,000 / yearFacilitates communication and collaboration with internal, cross-functional team members including, but not limited to, research, manufacturing, drug supply, regulatory, quality assurance, marketing and external key stakeholders including, but not limited to, collaborators, KOLs, investigators and domestic and international regulatory authorities, to support CDPs, regulatory submissions and clinical development goals. Clinical Research Organizations (CROs) and other vendors, consultants, collaborators, etc.); monitors program/study budgets to ensure the timely and cost-effective implementation of CDP(s); reviews and approves contracts, work orders and invoices within grant of authority; participates in the assessment of CROs, vendors, consultants or other partners as necessary.
NewSenior Director, AI & Clinical Science Medidata Solutions IncSenior Director, AI & Clinical ScienceNew York, NY$216,000–$288,000 / yearOperating at the intersection of AI, clinical science, product innovation, and software engineering, you will partner closely with leaders across Product, Engineering, Data, and Delivery to build AI capabilities that automate complex workflows, generate actionable insights from clinical data, and enable faster, smarter decisions across clinical development. You will remain hands-on in tackling high-impact technical problems, applying the latest advances in AI - including large language models, agentic AI, machine learning, and modern data platforms - to deliver intelligent solutions that accelerate every stage of the clinical trial lifecycle, from protocol design and trial simulation to study execution, monitoring, and clinical insights.
Senior Clinical Database Designer I Everest Clinical ResearchSenior Clinical Database Designer INew JerseyRemoteDevelop new features and functionality within the database design functional areas to increase the efficiency of database design at the study level, and to improve and enhance the company’s database design capabilities. Everest Clinical Research (“Everest”) is a full-service, global, contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries.
Senior Global Client Partner IQVIASenior Global Client PartnerParsippany, New YorkThe successful candidate will have a track record of success across most of the following competencies: 15+ years’ combined experience in Strategy Consulting, with a deep understanding of client engagement and solution delivery and/or; in the Pharma & Life Sciences commercial domain, with a deep understanding of business strategy and the processes of major pharmaceutical companies. Demonstrated success managing a balanced pipeline of short-term tactical opportunities and long-term strategic engagements, consistently exceeding ambitious sales targets across both single‑year and multi‑year deals.
Sr. Director, Global Account Management - Emerging Biopharma IQVIASr. Director, Global Account Management - Emerging BiopharmaParsippany, North CarolinaRemoteIn this commercial leadership role, you will be accountable for identifying, developing, and expanding customer relationships; creating new sales opportunities; and positioning IQVIA’s capabilities to help emerging biopharma companies advance development portfolios, scale effectively across markets, and achieve long-term growth. The Senior Director will lead account planning, pipeline development, opportunity shaping, and cross-functional sales orchestration while partnering closely with IQVIA delivery, data, technology, and commercial teams to create solutions that address customer priorities and deliver measurable value.
Senior Director, Quantitative Pharmacology Sun Pharmaceutical Industries LtdSenior Director, Quantitative PharmacologyPrinceton, NJ$215,500–$239,500 / yearThe 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.
Engagement and Communications, Sr. Manager Medidata Solutions IncEngagement and Communications, Sr. ManagerNew York, NY$135,000–$180,000 / yearCelebrating over 25 years of ground-breaking technological innovation across more than 38,000 trials and 12 million patients, Medidata offers industry-leading expertise, analytics-powered insights, and one of the largest clinical trial data sets in the industry. The ideal candidate will solidify the 'Insights-as-a-Product' model, ensuring that complex site, patient, and clinical insights are synthesized into high-impact narratives that align internal stakeholders and generate internal awareness and engagement and commercial value.
Senior Biostatistician Kenvue Brands LLCSenior BiostatisticianSkillman, NJFull timeThis support includes statistical aspects of study design, protocol review, and preparation of statistical sections; preparation of the statistical analysis plan; oversight of tables/listings/figures development; interpretation of results to internal clinical and management personnel; and assistance in the preparation of publications and submissions of regulatory deliverables. The Biostatistician in this role provides study-level statistical expertise in support of the design, analysis, and interpretation of clinical trials through collaboration with other team personnel including clinical research, clinical operations, data management, and programming.
NewSenior Proposal Manager Clinilabs IncSenior Proposal ManagerNY$115,000–$125,000 / yearThis role manages the proposal process from initial RFP intake through final submission, working cross-functionally with Business Development, Operations, Finance, Legal, Contracts, and other subject matter experts to ensure proposals are accurate, competitive, compliant, and aligned with sponsor requirements. Ability to review and interpret protocols/SOAs, RFP materials, sponsor requirements, bid grids, assumptions, scopes of work, vendor inputs, and operational feedback to support accurate pricing, comprehensive budget development, risk identification, proposal strategy, and alignment with clinical trial operational requirements.
Senior Manager R&D Quality Analytics & Portfolio Insights BeOne Medicines AGSenior Manager R&D Quality Analytics & Portfolio InsightsNY$136,500–$181,500 / yearThese may include statistical monitoring, predictive risk models, anomaly-detection methods, patient-safety and adverse-event reporting analytics, data-informed audit packages, risk indicators, dashboards, automated monitoring, natural-language tools, and other scalable capabilities that support Quality by Design, Risk-Based Quality Management, audit and inspection readiness, vendor, process, and system oversight, and targeted risk mitigation. Develop analytical approaches to support data-informed audit planning/execution and identify potential patient-safety and subject-protection risks, including adverse-event under-reporting or over-reporting, unusual clinical-event patterns, protocol-compliance concerns, data-quality issues, and other signals requiring targeted Quality review.
Senior Product Manager, IQVIA Digital IQVIASenior Product Manager, IQVIA DigitalParsippany, PennsylvaniaThrough close partnership with clients and cross-functional collaboration with Go-to-Market, Technology, Data Management, and Operations teams, the team translates market insights and customer needs into innovative, scalable products. You will collaborate closely with Media Partnerships, Sales leaders, Advanced Analytics, Engineering, and Client teams to ensure our measurement products are rigorous, differentiated, and aligned with evolving client and market needs.
Senior Software Engineer (React), IQVIA Digital IQVIASenior Software Engineer (React), IQVIA DigitalRed Bank, New JerseyBuilt on IQVIA's industry-leading healthcare data assets and privacy-by-design principles, the team leverages modern engineering, cloud, and artificial intelligence technologies to accelerate innovation, enhance product capabilities, and deliver differentiated solutions that create measurable value for clients across the healthcare ecosystem. This is an exciting opportunity for an experienced engineer who thrives in a fast-paced, agile environment, enjoys solving complex technical challenges, and is passionate about driving technical excellence and mentoring team members.
Senior Director, Regional Clinical Study Management BeOne Medicines AGSenior Director, Regional Clinical Study ManagementNY$206,200–$276,200 / yearGeneral Description: As part of the regional leadership team, provides inspirational leadership, proactive management, and feedback-oriented mentorship to clinical study managers at various levels for assigned portfolio and may lead a designated therapeutic area or asset. Shapes and influences strategies to ensure that the clinical studies are operationally feasible in the region, optimizes trial feasibility, country allocation and site selection process for assigned region in collaboration with feasibility managers, country heads, medical affairs and any other stakeholders.
Senior Medical Director BIOUS BioLumina GroupSenior Medical DirectorNew York, New YorkThe Senior Medical Director must demonstrate clinical and technical knowledge of medicine across a broad range of oncology-focused therapeutic areas, and will provide medical direction across agency departments and reviewwork for scientific accuracy and strategic relevance. Organize database of potential key opinion leader contacts; conduct advisory boards, develop medical content in the form of discussion guide for focus groups and telephone interviews with opinion leaders and other physicians.