NewCT Technologist Jefferson HealthCT TechnologistCamden, NJJefferson is more than 65,000 people strong, dedicated to providing the highest-quality, compassionate clinical care for patients; making our communities healthier and stronger; preparing tomorrow's professional leaders for 21st-century careers; and creating new knowledge through basic/programmatic, clinical and applied research. Thomas Jefferson University, home of Sidney Kimmel Medical College, Jefferson College of Nursing, and the Kanbar College of Design, Engineering and Commerce, dates back to 1824 and today comprises 10 colleges and three schools offering 200+ undergraduate and graduate programs to more than 8,300 students.
NewRadiology Technician Jefferson HealthRadiology TechnicianCamden, NJJefferson is more than 65,000 people strong, dedicated to providing the highest-quality, compassionate clinical care for patients; making our communities healthier and stronger; preparing tomorrow's professional leaders for 21st-century careers; and creating new knowledge through basic/programmatic, clinical and applied research. Thomas Jefferson University, home of Sidney Kimmel Medical College, Jefferson College of Nursing, and the Kanbar College of Design, Engineering and Commerce, dates back to 1824 and today comprises 10 colleges and three schools offering 200+ undergraduate and graduate programs to more than 8,300 students.
Perm - Physician - Otolaryngology Egg Harbor Township, NJ VieMed Healthcare StaffingPerm - Physician - Otolaryngology Egg Harbor Township, NJEgg Harbor Township, NJThis leadership role provides a unique opportunity to impact clinical care, research, and community outreach, with start dates available immediately or soon after application. This leadership role at a prominent hospital in Egg Harbor Township offers a vibrant coastal environment, state-of-the-art surgical facilities, and a commitment to innovation and excellence.
Operations Director, Clinical Laboratory Operations - Clinical Laboratory Administration - Tri State Area (New York, New Jersey, Connecticut) - Full Time/Day Shift Mount Sinai Health SystemOperations Director, Clinical Laboratory Operations - Clinical Laboratory Administration - Tri State Area (New York, New Jersey, Connecticut) - Full Time/Day ShiftNewark, NJMount Sinai advances health for all people, everywhere, by taking on the most complex health care challenges of our time - discovering and applying new scientific learning and knowledge; developing safer, more effective treatments; educating the next generation of medical leaders and innovators; and supporting local communities by delivering high-quality care to all who need it. We are consistently ranked by U.S. News & World Report's Best Hospitals, receiving high "Honor Roll" status, and are highly ranked: No. 1 in Geriatrics, top 5 in Cardiology/Heart Surgery, and top 20 in Diabetes/Endocrinology, Gastroenterology/GI Surgery, Neurology/Neurosurgery, Orthopedics, Pulmonology/Lung Surgery, Rehabilitation, and Urology.
Clinical Study Manager, Global Clinical Operations - 30014765 Daiichi Sankyo Co LtdClinical Study Manager, Global Clinical Operations - 30014765Basking Ridge, NJ$133,600–$200,400 / yearCRO Oversight: Responsible for the oversight, performance, and management of CRO(s) and 3rd party vendors (sub-contracted by CRO) to ensure compliance with Daiichi Sankyo's quality measures and adherence to scope of work within timelines and budget at a task level. Clinical Operations Study Management(Global) has primary accountability for operational execution and delivery of assigned clinical trials, including study level time, cost and quality deliverables.
2027 Future Talent Program - Global Clinical Trial Operations Epidemiology Operations - Intern Merck & Co Inc2027 Future Talent Program - Global Clinical Trial Operations Epidemiology Operations - InternRahway, NJ$39,908–$111,111 / yearThe intern will engage with the Epidemiology Operations organization and their associated project teams throughout participation in and/or leadership of initiatives that drive the efficient and ethical conduct of epidemiology trials across GCTO. Required Education: Candidates must be currently enrolled in a full-time BS/BA (or higher) degree program in a business or project management, continuous improvement, computer technology, or science related discipline.
Associate Director, Clinical Operations Protagonist TherapeuticsAssociate Director, Clinical OperationsNewark, New JerseyThe Company also has a number of preclinical stage drug discovery programs addressing clinically and commercially validated targets including an oral IL-17 peptide antagonist, obesity dual and triple agonists, an oral hepcidin functional mimetic, and the recently announced IL-4 and amylin programs. The base pay range for this position at commencement of employment is expected to be between $185K and $205K / year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience.
Associate Clinical Programmer - Clinical Data Operations Novartis AGAssociate Clinical Programmer - Clinical Data OperationsEast Hanover, NJ$27,900–$51,900 / yearRead our brochure to learn more about our global total rewards offering: https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdfNote : Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. Expected Annual Base Salary Range for role: € 27,900.00 - 51,900.00 The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically.
Senior Scientist, Regulatory & Clinical Operations hims & hersSenior Scientist, Regulatory & Clinical OperationsSouth Plainfield, NJYou Have: PhD in Clinical Chemistry, Biochemistry, Analytical Chemistry, Molecular Biology, or related field with 4+ years; OR Master's degree with 7+ years; OR Bachelor's degree with 10+ years of relevant bench experience in a diagnostic or clinical laboratory setting. The ideal candidate is comfortable operating at the intersection of bench science and clinical study execution, translates regulatory rigor into practical day-to-day decisions, and thrives working independently in a fast-moving environment.
NewGlobal Clinical Operations AI Program Associate Director NovartisGlobal Clinical Operations AI Program Associate DirectorEast HanoverAI Adoption, AI Adoption, Artificial Intelligence (AI), Artificial Intelligence Software, Artificial Intelligence Strategy, Artificial Intelligence Techniques, Biostatistics, Business Value Creation, Change Management, Change Management for AI Adoption, Clinical Operations, Clinical Research Operations, Clinical Trials Operations, Curious Mindset, Data Governance, Data Literacy, Data Quality, Data Science, Data Visualization, Deep Learning, Good Clinical Practice (GCP), Graph Algorithms, Learning Agility, Machine Learning (ML), Machine Learning Algorithms {+ 4 more} This position acts as the programmatic backbone of the AI team by supporting the coordination and alignment of GCO AI product roadmaps with Dev AI products and strategy as well as enabling Product Owners, Platform Leads and the Head of AI Transformation to deliver on the GCO AI goals.
NewGlobal Clinical Operations AI Product Director NovartisGlobal Clinical Operations AI Product DirectorEast HanoverAI Product Management, Artificial Intelligence (AI), Artificial Intelligence Software, Artificial Intelligence Strategy, Artificial Intelligence Technologies, Business Value Creation, Change Management, Clinical Operations, Clinical Research Operations, Clinical Trials Operations, Curious Mindset, Data Governance, Data Literacy, Data Quality, Data Science, Data Visualization, Deep Learning, Learning Agility, Machine Learning (ML), Machine Learning Algorithms, Mentorship, Pharmaceutical Industry, Stakeholder Engagement, Statistical Analysis, Time Series Analysis Working at the intersection of clinical operations, technology, and business strategy, you will guide products from concept through adoption, ensuring they are compliant, user-focused, and capable of delivering measurable value.
Associate Director, Clinical Operations Summit Therapeutics IncAssociate Director, Clinical OperationsPrinceton, NJ$174,000–$205,000 / yearHARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI. Drafts, reviews and approves internal and external study-related plans, processes, and documents including Informed Consent Forms, Investigator Agreements (CTA), CRFs, CRF Guidelines, statistical/pharmacokinetic analysis plans, monitoring plans, data management plans, and safety monitoring activities.
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.
Contract, Clinical Operations PTC Therapeutics IncContract, 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.
Clinical Research Operations Manager - Oncology VitaliefClinical Research Operations Manager - OncologySomerset, NJFull timeBy combining deep subject matter expertise with the experience of senior research practitioners, we help organizations accelerate study activation, optimize operations, improve financial performance, and build scalable workforce solutions that reduce costs, increase efficiency, and advance clinical breakthroughs for patients. IMPORTANT NOTE: Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis.
Senior Clinical Quality Operations Manager Eikon Therapeutics IncSenior Clinical Quality Operations ManagerJersey City, NJ$157,000–$189,000 / yearThis includes ensuring consistent execution of quality-by-design (QBD) principles across assigned clinical development programs and facilitating identification of Critical to Quality (CtQs) factors and associated risk assessments, establishing, and actively maintaining study-specific quality plans throughout the study lifecycle using a risk-based approach. In partnership with the Director of Process Management for Clinical R&D, the Head of Clinical Data Analytics and Reporting and the Head of Clinical Study Management, builds proficiency in leveraging technology and data to recognize and respond to new and emerging risks across the clinical portfolio, including how GCP applies to digital data management and novel trial technology.
Senior Director, Clinical Operations Mitsubishi Tanabe PharmaSenior Director, Clinical OperationsJersey City, NJWorking with closely with the Head of Clinical Development and the Development Team Leader(s), the Senior Director, Clinical Operations directs global clinical operational activities for MTDA, guiding activities and influencing colleagues in a highly matrixed environment. Provide clinical trial oversight and management, vendor and CRO performance (including bid/contract, budget/adjudication) and regulatory quality delivery of MTDA clinical trials according to corporate processes and timelines.
2027 Future Talent Program - Clinical Business Operations - Intern Merck & Co Inc2027 Future Talent Program - Clinical Business Operations - InternRahway, NJ$39,908–$111,111 / yearClinical Data Management is the practice of defining, designing, implementing, investigating, cleaning end ensuring that data collected in support of the needs of a clinical research trial satisfy the analysis and reporting requirements necessary to satisfy (regulatory requirements) of the planned Clinical Study Report. Business Operations supports the GDMS organization in the areas of Portfolio & Resource Operations, Project Management, Change Management, Communications, Learning & Development and Metrics/KPIs.
Senior Scientist, Regulatory & Clinical Operations Hims & HersSenior Scientist, Regulatory & Clinical OperationsSouth Plainfield, New JerseyPhD in Clinical Chemistry, Biochemistry, Analytical Chemistry, Molecular Biology, or related field with 4+ years; OR Master’s degree with 7+ years; OR Bachelor’s degree with 10+ years of relevant bench experience in a diagnostic or clinical laboratory setting. The ideal candidate is comfortable operating at the intersection of bench science and clinical study execution, translates regulatory rigor into practical day-to-day decisions, and thrives working independently in a fast-moving environment.
Data Engineer, Clinical Operations Bristol Myers SquibbData Engineer, Clinical OperationsPrinceton, NJ$87,810–$106,399 / yearKey Responsibilities: Collaborate with BI&T partners, cross-study operations leads, specimen management specialists, clinical study teams, clinical trial analysts, trial managers, domain experts, and cross-functional leaders in data engineering, data product teams, and data operations to support effective adoption of our Data Platform. Develop and operationalize cloud-based GenAI and LLM-powered applications in collaboration with data product owners, engineers, and data scientists, utilizing techniques such as RAG, fine-tuning, and vector embeddings to deliver high-quality data discovery and consumption features for cross-study and specimen management workflows.