Site Enrollment and Engagement Lead - Licensed Medical Professionals IQVIASite Enrollment and Engagement Lead - Licensed Medical ProfessionalsParsippany, KansasThe Site Enrollment and Engagement Lead (formerly the Clinical Trial Educator (CTE)) will provide information and education on clinical trial inclusion and exclusion criteria to trial coordinators and healthcare providers. This position also requires the Site Enrollment and Engagement Lead to work with referring physicians and develop referral networks to support the sites, as well as work with support groups in the therapeutic area.
Program Coordinator Columbia UniversityProgram CoordinatorNew York, NY$65,000–$76,000 / yearThe Division of Pediatric Hematology, Oncology and Stem Cell Transplantation (SCT) at Columbia University Irving Medical Center (CUIMC) within the Integrative Therapies Program (ITP) and International Initiative for Pediatrics and Nutrition (IIPAN) is recruiting a Program Coordinator to contribute to two established programs related to clinical care and research in integrative health and nutritional global health. Reporting to the principal investigator (PI), the Project Coordinator will: Develop, adopt, and implement the protocols of clinical research studies, including subject recruitment/follow-up and data collection.
Sr Mgr Clinical Drug Supply & Logistics Regeneron Pharmaceuticals IncSr Mgr Clinical Drug Supply & LogisticsArmonk, NY$134,400–$219,200 / yearPrepares or provides input into IP-related content for training materials and coordinates training on study procedures; In collaboration with the CTM for study, provides input into IP-related study specific working practices; Establishes study team contacts, roles, responsibilities, and objectives for IP-related services; Develops, manages, and maintains relationships with external partners; Effectively communicates with CROs, shipping and IVRS vendors, study sites and study team members to ensure ongoing successful execution; Acts as point of escalation for IP-related issues. Build our future together: The Senior Manager, Clinical Drug Supply & Logistics is responsible for providing oversight of individual or multiple clinical programs, forecasting Investigational Product (IP) supply requirements for multiple clinical trials, and for managing the IP distribution process to one or more clinical trials.
Director/Senior Director, Clinical Development MD Axsome Therapeutics IncDirector/Senior Director, Clinical Development MDNew York, NYRemote$240,000–$300,000 / yearOur industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, and multiple late-stage development programs addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in the United States. The Director/Senior Director, Clinical Development will help shape clinical strategy, contribute to protocol design and key regulatory and clinical documents, and serve as a clinical representative with regulators, investigators, and cross-functional partners.
NewRegistered Nurse (R.N.) - Intensive Care Unit Newark Wayne Community Hospital & DeMayRegistered Nurse (R.N.) - Intensive Care UnitNewark, New Jersey$39.74–$52.99 / hourJob Title: R.N.- Intensive Care Unit Department: Intensive Care Unit Location: Newark Wayne Community Hospital Hours Per Week: Part Time (24 hours per week) Schedule: Evening/Night (6pm-6am), rotating weekends and holidays. RN Level IV: Minimum 1 year experience in the specialty hired into; BS in Nursing required; expanded leadership role (charge, preceptor, mentor); completion of Clinical Ladder requirements within 12 months, including 5 activities per pillar, 15 CEUs, and 20 flex items.
Security Research Engineer PensarSecurity Research EngineerNew York, New York$120,000–$175,000 / yearIn parallel, you'll drive original offensive and open source security research, and feed everything you learn in the field back into the product so Pensar keeps getting sharper as a pentesting platform. You'll be on the front lines of customer engagements — using our open source tool Apex to run pentests, curate and present findings, and stand up our platform inside customer environments.
Clinical Research Associate (Multiple Roles) Novartis AGClinical Research Associate (Multiple Roles)NY$32,690–$60,710 / 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: 32,690 - 60,710 GBP AnnualThe 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.
Clinical Research Coord I Columbia UniversityClinical Research Coord INew York, NY$66,300–$72,000 / yearCoordinates with laboratory researchers, pathologists, pathology technicians, and surgeons to obtain samples from the cystoscopy suite and operating room, including the acquisition of rare and high priority biospecimens from GU medical oncology patients. This role will coordinate complex workflows across concurrent studies, applying judgment to prioritize tasks and address challenges as they arise; it will also contribute to process improvements and support guidance of new research staff.
Clinical Research Coordinator I - General Medicine Columbia UniversityClinical Research Coordinator I - General MedicineNew York, NY$66,300–$67,000 / yearThe Division of General Medicine seeks a full-time Clinical Research Coordinator (CRC) to assist with clinical research studies related to obesity and cardiometabolic health. Assist with and lead study visits, including administering questionnaires, overseeing behavioral tests, providing wearable devices, and processing biospecimens.
NewClinical Research Coordinator- Part Time New York University School of MedicineClinical Research Coordinator- Part TimeNew York, NY$38.72–$45.87 / hourJob Responsibilities: Patient Recruitment and Scheduling: Actively engage, screen and recruit patients for the study, ensuring that all participants meet the studys specific inclusion criteria. For 175 years, NYU Grossman School of Medicine has trained thousands of physicians and scientists who have helped to shape the course of medical history and enrich the lives of countless people.
Clinical Research Coordinator - Endocrinology (NYNORC) Columbia UniversityClinical Research Coordinator - Endocrinology (NYNORC)New York, NYThe Clinical Research Coordinator will report to the Principal Investigator/Core Laboratory Director and work collaboratively with the team to perform human body composition measurements and indirect calorimetry assessments in volunteer participants enrolled in ongoing research studies. Clinical Research Coordinator - Endocrinology (NYNORC) 555556 Columbia University Medical Center Medicine Full Time Opening on: Feb 20 2026 Grade 103 Add to favorites View favorites.
Clinical Research Coordinator I - Cardiology (CARE) Columbia UniversityClinical Research Coordinator I - Cardiology (CARE)New York, NY$69,500–$72,500 / yearThe Clinical Research Coordinator I is an intermediate level position that provides independent study coordination for simple and moderately complex clinical research studies such as registries, retrospective data reviews, studies in long-term follow-up, and other non-interventional studies or under supervision provides study coordination for moderate complexity to high complexity clinical trials with supervision such as such as EFS and pivotal IDE/IND studies. Decision Making/Autonomy: Carries out research projects per guidelines and regulation with limited supervision, collaborating both independently and with the Principal Investigator (PI) and Clinical Research Manager.
Program Lead, Clinical Research New York University School of MedicineProgram Lead, Clinical ResearchNew York, NY$84,577.93–$101,223.89 / yearProvides strategic and operational leadership for end-to-end study start-up and activation activities across the CTSI Clinical Research Centers portfolio, including protocol intake, feasibility review, operational assessments, budget development, regulatory coordination, and activation readiness. Collaborates with investigators, departmental leadership, OSR units, contracts, sponsored programs, billing compliance, IRB, finance offices, and institutional service providers to ensure alignment across contractual, operational, financial, and regulatory timelines.
Clinical Research Coordinator Columbia UniversityClinical Research CoordinatorNew York, NY$64,350–$65,000 / yearThe CRC will work with investigators, study staff, Scientific Review Committee (SRC) and institutional review boards (IRB), clinical trial sponsors and federal regulatory agencies to assure compliance with study protocols, data documentation, reporting requirements, ensure that regulatory requirements for clinical trials are met. Prepares and submits regulatory documentation that may include IND/IDE applications, FDA annual reports, Serious Adverse Event reports, to the appropriate regulatory agencies including the Food and Drug Administration (FDA) etc.
Clinical Research Aide Columbia UniversityClinical Research AideNew York, NYThe responsibilities for the position include: After training: The incumbent will conduct study procedures but not limited to conducting and completing screeners to determine study eligibility; verify, enroll, and consent eligible participants; completing follow-ups and reminders in person and remotely which will include study interview administration as assigned; administration of study assessments to include questionnaires and obtaining biospecimens. The candidate will learn the operations of a research study from developing culturally appropriate data collection measures, participant recruitment and retention, and data collection to address study aims and hypothesis.
Clinical Research Coordinator - Cardiology Columbia UniversityClinical Research Coordinator - CardiologyNew York, NY$66,300–$68,300 / yearThe CRC will collaborate closely with faculty investigators, research fellows, a regulatory manager, a biostatistician, and a data manager to execute high‑quality academic clinical research and contribute to scholarly dissemination. The salary of the finalist selected for this role will be set based on a variety of factors, including but not limited to departmental budgets, qualifications, experience, education, licenses, specialty, and training.
Clinical Research Coordinator - Endocrinology Columbia UniversityClinical Research Coordinator - EndocrinologyNew York, NYThe CRC will be responsible for coordinating patient participation activities, including screening, recruitment, enrollment, assessment, and follow-up of study participants; collecting and maintaining study data; ensuring adherence to study protocols and regulatory requirements; and collaborating with investigators, sponsors, and research staff to facilitate the successful conduct of clinical research. Maintain complete and accurate research records, including study regulatory files, case report forms (CRFs), study logs, source documentation, questionnaires, adverse event (AE) reports, and study start-up and close-out documentation.
NewClinical Research Coordinator II Columbia UniversityClinical Research Coordinator IINew York, NYWorking in the Clinical Protocol & Data Management office in the Herbert Irving Comprehensive Cancer Center under the direct supervision of the Clinical Research Manager (CRM) or the specific disease site this incumbent is assigned to, the Clinical Research Coordinator (CRC) II will support the coordination of clinical research activities according to clinical research studies or trials managed by the department. In general, the CRC II will be responsible for the coordination of patient participation (including screening, recruitment, assessment, and follow-up of study participants), collection and maintenance of study data, ensuring adherence to study activities as described in the protocol, and working with other members of the research team to coordinate all other aspects related to the conduct of the clinical trial or study.
Senior Clinical Research Coordinator New York University School of MedicineSenior Clinical Research CoordinatorNew York, NY$70,481.61–$88,236.75 / yearThe Senior Clinical Research Coordinator (Senior CRC) serves as a senior research coordinator for the Eosinophilic Gastrointestinal Diseases (EGID) Program at NYU, directed by Mirna Chehade, MD, MPH, and is responsible for the day-to-day execution and coordination of a diverse clinical research portfolio focused exclusively on EGIDs. Familiar with Internet applications Intermediate competency in medical terminology, and 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.
NewClinical Research Site Manager, HBN (2273) Stone Alliance GroupClinical Research Site Manager, HBN (2273)New York, New YorkSite Operations & Maintenance – Oversee day-to-day functioning of Harlem and Staten Island offices, including space and resource assignments, inventory management, and HR/Facilities/IT coordination to ensure smooth site operations. You will oversee all daily activities and operations, including capacity management, optimized scheduling and flow of participants, facility performance, participant safety, onboarding coordination, and coordination of resources.