NewClinical Research Coordinator (Long Island, NY) SiteBridge Research, Inc.Clinical Research Coordinator (Long Island, NY)Long Island, NYFounded in 2021, SiteBridge Research (SBR) is an integrated research organization, building a national network of small and community practices to deliver world-class industry sponsored clinical research on time and on budget, accelerating time to market and product adoption in communities that are hardest to reach. The role involves close collaboration with the site team, sponsors, and clinical monitors to ensure ICH/GCP compliance, optimize site efficiency, and support timely study completion.
Research Assistant Weill Cornell Medical CollegeResearch AssistantNew York, NY$22.03–$30 / hourCornell welcomes students, faculty, and staff with diverse backgrounds from across the globe to pursue world-class education and career opportunities, to further the founding principle of "any person, any study." Cornell University embraces diversity in its workforce and seeks job candidates who will contribute to a climate that supports students, faculty, and staff of all identities and backgrounds.
NewEquity Research Senior Associate Healthcare Technology & Distribution Citigroup IncEquity Research Senior Associate Healthcare Technology & DistributionNew York, NY$150,000–$175,000 / yearThe unit produces regular written research on healthcare technology and distribution companies, hosts investor meetings with company management teams, holds conference calls with industry consultants (including clinicians, health system executives, and policy experts), and regularly communicates with clients (both internal and external). Appropriately assess risk when business decisions are made, demonstrating particular consideration for the firm's reputation and safeguarding Citigroup, its clients, and assets, by driving compliance with applicable laws, rules, and regulations, adhering to Policy, applying sound ethical judgment regarding personal behavior, conduct, and business practices, and escalating, managing, and reporting control issues with transparency.
Global 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.
Clinical Review Specialist - Fully Remote MercorClinical Review Specialist - Fully RemoteNew York, New YorkRemoteManage end-to-end prior authorisation workflows for medical and clinical services across multiple payer types. 5+ years of experience in prior authorisation, utilisation management, or clinical review, with at least 2 years in a management role.
Principal Scientist - Clinical and Scientist Affairs Estee Lauder IncPrincipal Scientist - Clinical and Scientist AffairsMelville, NY$110,000–$125,000 / yearThe company's products are sold in approximately 150 countries and territories under brand names including: Estée Lauder, Aramis, Clinique, Lab Series, Origins, M·A·C, La Mer, Bobbi Brown Cosmetics, Aveda, Jo Malone London, Bumble and bumble, Darphin Paris, TOM FORD, Smashbox, AERIN Beauty, Le Labo, Editions de Parfums Frédéric Malle, GLAMGLOW, KILIAN PARIS, Too Faced, Dr. Jart+, the DECIEM family of brands, including The Ordinary and NIOD, and BALMAIN Beauty. This individual will play a critical role in translating marketing consumer concepts into actionable and scientifically supportable data, and also translating complex scientific data into compelling product stories, ensuring scientific credibility while aligning with brand strategy and consumer expectations.
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.
Director, Clinical Data Management Nektar TherapeuticsDirector, Clinical Data ManagementNY$240,000–$275,000 / yearDirects planning and execution of clinical trial data management activities including CRF/eCRF design, database development, validation programming, discrepancy management, and database release. Nektar currently anticipates the base salary for the Director, Regulatory Affairs to range from $240,000 to $275,000 for candidates in the Bay Area and will depend, in part, on successful candidates location and qualifications for the role, including education and experience.
CDI Leader - Clinical Documentation MercorCDI Leader - Clinical DocumentationNew York, New YorkRemoteMonitor CDI program KPIs, including query response rates, CC/MCC capture rates, case mix index, and DRG accuracy. 5+ years of experience in clinical documentation integrity or improvement, with 2+ years in a manager or leadership role.
Quality Assurance Specialist - Clinical Trial Supply JUPITER RESEARCH SERVICES INCQuality Assurance Specialist - Clinical Trial SupplyEdison, NJFull timeThe Quality Assurance Specialist – Clinical Trial Supply plays a critical role in ensuring the quality, safety, integrity, and compliance of clinical trial materials throughout their lifecycle—from receipt and storage to packaging, labeling, distribution, and returns. The QA Specialist ensures that all products and processes meet regulatory and customer expectations while supporting JRS’s mission to deliver reliable, resilient, and high-quality clinical supply solutions worldwide.
Healthcare Expert - Clinical Evaluator MercorHealthcare Expert - Clinical EvaluatorNew York, New YorkRemote$90–$100 / hourFor details about the interview process and platform information, please check: https://talent.docs.mercor.com/welcome. Mercor connects elite creative and technical talent with leading AI research labs.
Care Management Associate - LTSS - Work at Home CVS Health CorpCare Management Associate - LTSS - Work at HomeNJ$18.50–$38.82 / hourPosition Summary: This work at home role as a Care Management Assistant, you will support the coordination of member healthcare services by assisting with intake, screening, and triage of care team tasks, while helping ensure that members receive timely, appropriate care. Your role includes maintaining accurate and compliant documentation within internal systems, conducting non‑clinical research to support case activity, and monitoring cases for needed follow‑up or program referrals.
Visiting Assistant Professor, Clinical Mental Health Counseling Touro University New YorkVisiting Assistant Professor, Clinical Mental Health CounselingNew York, New YorkFull timeCandidates preferred to have a doctoral degree in counseling, counselor education, or a related field from a CACREP-accredited program OR have taught for a minimum of one full year in a counseling program prior to July 1, 2013. SPSS skills essential, data analysis knowledge in Excel a plus CANVAS educational platform Internet journal library and google scholar search experience (Preferred).
Director, External Scientific Society Engagement Revolution Medicines IncDirector, External Scientific Society EngagementNY$201,000–$251,000 / yearThe company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. Partner cross-functionally with Medical Affairs, Clinical Development, Translational Medicine, Research, Medical Communications, HEOR, Market Access, Commercial, and Field Medical teams to align external engagement strategies with enterprise priorities.
Per Diem Integrative Yoga Practitioner (FGP) - Manhattan, Center for Women's Health NYU Langone Medical CenterPer Diem Integrative Yoga Practitioner (FGP) - Manhattan, Center for Women's HealthNew York, NY$29.28–$50.51 / hourProgram Design & Clinical Operations: Collaborate with the clinical team and Program Manager to develop and refine mind-body clinical pathways and group visit offerings (e.g., stress management series, peri/menopause support, survivorship programs). Clinical Mind-Body Services: Provide individually tailored yoga sessions for patients with a variety of conditions (e.g., womens health concerns, chronic musculoskeletal pain, cancer survivorship, stress and sleep challenges), with appropriate modifications and safety considerations.
Clinical Research Coordinator, Research Biofluid Management Unit; Monday-Friday, 11AM - 7PM * Oncology clinical research experience preferred * New York University School of MedicineClinical Research Coordinator, Research Biofluid Management Unit; Monday-Friday, 11AM - 7PM * Oncology clinical research experience preferred *New York, NY$70,481.60–$76,450 / yearIntermediate competency in medical terminology, and an advanced competency in Good Clinical Practice (GCP) guidelines, Federal Regulation that govern the conduct of human subjects research as well as Institutional Review Board and institutional policies and procedures related to human subjects research. Record, update, edit, and maintain confidential information relating to research biospecimens onto paperwork and/or web-based forms in a neat, accurate and timely manner and ensure subsequent data collection as required.
FSP Sr. Clinical Research Associate II - NYC Metro or PHL - Onc Fortrea IncFSP Sr. Clinical Research Associate II - NYC Metro or PHL - OncNew York, NYRemote$125,000–$140,000 / yearResponsibilities: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.
Clinical Research Nurse I - Oncology * Must have oncology clinical trials experience * New York University School of MedicineClinical Research Nurse I - Oncology * Must have oncology clinical trials experience *New York, NY$105,000–$125,000 / yearThe primary purpose of the subspecialized oncology clinical research nurse role is to facilitate positive outcomes of safety and quality for patients enrolled on adult oncology clinical trials at the NYU Perlmutter Cancer Center by coordinating and managing patients enrolled on clinical trials by employing the nursing process, clinical skills, critical thinking, evidence-based nursing and an understanding the scientific research. Utilizing the nursing process, nursing assessment skills and critical thinking the Oncology CRN I conducts a thorough research screening visit for potential trial participants per the protocol requirements, including but not limited to a Review of Systems (ROS), baseline and ongoing AE assessment and documentation, and collection of concomitant medications and documents the assessments in the EPIC electronic health record per CTO policies and procedures.
Clinical Research Finance Analyst - Clinical Trial Billing New York University School of MedicineClinical Research Finance Analyst - Clinical Trial BillingNew York, NY$70,481.60–$75,000 / yearThis position liaises with internal and external customers, consults with faculty, the Clinical Research Support Unit, and Departmental Administrative personnel regarding billing, accounts receivable, payment reconciliation and accurate and timely completion study closure process. This position provides post-award financial management of industry sponsored clinical trials, ensuring accurate and timely payments from clinical trial sponsors.