Clinical Research Project Manager iMPact Business GroupClinical Research Project ManagerMahwah, NJLeading people who perform project management duties involving cross-functional teams focused on delivering internal products or administrative systems. Organizing project activities and interdepartmental meetings, ensuring communication facilitates the completion of the program or project on schedule and within budget constraints.
Senior Clinical Study Manager Integrated Resources, IncSenior Clinical Study ManagerWoodcliff Lake, New JerseyFull timeCollaborate with other team members to coordinate the development and finalization of key study documents including protocols, case reports forms, informed consent documents, study management plans and final clinical study reports. Oversee Clinical Trial Coordinator for assigned project to ensure successful management of project(s), including development of the project plan, maintenance of trackers, and generation of metrics reports.
Senior Clinical Study Manager (Hybrid) StrykerSenior Clinical Study Manager (Hybrid)Mahwah, New Jersey$132,100–$220,100 / yearAs Senior Clinical Study Manager, you will serve as the cross-functional project leader responsible for delivering clinical research business initiatives through effective project execution, stakeholder engagement, process improvement, technology implementation, and compliance-focused operational support. Experience implementing or optimizing clinical technology platforms such as clinical trial management systems, electronic data capture systems, electronic trial master files, electronic clinical outcome assessment tools, analytics, reporting, or quality management systems.
Clinical Data Manager Integrated Resources, IncClinical Data ManagerWoodcliff Lake, New JerseyFull timePerform DM activities for in-house and outsourced trials: protocol review, CRF development, database set up activities, data validation process (including manual data review of listings), SAE reconciliation, managing local laboratory and external labs and database lock. Bachelor degree or above in scientific or related field Minimum 5-7 years' experience in Data Management with experience in managing projects, project teams.
Senior Clinical Data Manager Integrated Resources, IncSenior Clinical Data ManagerWoodcliff Lake, New JerseyFull timeCoordinates and conducts setup activities, such as CRF design for complex trials, database structure design, CRF annotation, project document creation and/or approval, data entry screen design and testing, validation check creation, testing and approval. • Perform DM activities for in-house and outsourced trials: protocol review, CRF development, database set up activities, data validation process (including manual data review of listings), SAE reconciliation, managing local laboratory and external labs and database lock.
Clinical Research Scientist Integrated Resources, IncClinical Research ScientistWoodcliff Lake, New JerseyContractorPrepare and review project and study documents including clinical trial protocols, clinical study reports, patient SAE narratives, clinical sections of registration dossier documents (ISS, ISE, Investigator Brochure, etc). In collaboration with other clinical staff and/or an external CRO, monitoring clinical trial conduct (enrollment, GCP practices, handling of safety issues, etc.).
Senior Manager, Clinical Scientist, Immunology Regeneron PharmaceuticalsSenior Manager, Clinical Scientist, ImmunologyTarrytown, NY$150,500–$245,500 / yearIn this role, you will help lead the design, execution, and interpretation of clinical studies, partnering closely with Medical Directors and cross-functional study teams to advance candidates through early and/or late phase development. This role requires: MS, PhD, or PharmD in a related scientific field, plus 8+ years of pharmaceutical clinical drug development experience (other levels considered based on experience).
NewSpec 3, Clinical Research Kaygen Inc.Spec 3, Clinical ResearchFranklin Lakes, NJ$40–$54 / hourWe specialize in providing high-volume contingent staffing, direct hire staffing and project-based solutions to companies worldwide ranging from startups to Fortune 500 and Managed Service Providers (MSP) across a wide variety of industries. Works with many different disciplines (manufacturing, marketing, quality, regulatory, etc.), materials, products and processes in the development of core clinical laboratory and outside the core clinical laboratory products and services.
Medical Director, Clinical Development, Solid Tumor Oncology (Gyn Oncology) Regeneron PharmaceuticalsMedical Director, Clinical Development, Solid Tumor Oncology (Gyn Oncology)Tarrytown, NY$284,900–$385,700 / yearIn this role, you will design clinical study concepts, oversee the medical and scientific supervision of clinical trials, and lead the Clinical Team to deliver high-quality program milestones, while collaborating with Clinical Project Managers, Clinical Trial Managers, and Therapeutic Area Program Managers. We are seeking a Medical Director, Clinical Sciences to join our Oncology team, supporting solid tumor drug development, including studies in ovarian cancer.
Executive Medical Director, Clinical Program Lead, Immunology / Rheumatology Regeneron PharmaceuticalsExecutive Medical Director, Clinical Program Lead, Immunology / RheumatologyTarrytown, NY$390,000–$527,600 / yearDiscover your role: Acts as medical expert and leader in interactions with external collaborators (e.g., regulatory authorities, key opinion leaders, advisory boards, patient advocacy groups), internal collaborators (e.g., Research, Early Clinical Development, Global Medical Affairs, Marketing, HEOR), and internal decision boards. Uses excellent scientific standing among peers and the ability to address issues with scientific rigor and creative solutions; uses that creativity and knowledge to build and defend data-driven plans and decisions, both with internal scientific management and the Company's partners/collaborators.
Executive Medical Director, Clinical Program Lead, Hematology Oncology Cell Therapy Regeneron PharmaceuticalsExecutive Medical Director, Clinical Program Lead, Hematology Oncology Cell TherapyTarrytown, NY$390,000–$527,600 / yearDiscover your role: Acts as medical expert and leader with external collaborators (regulatory authorities, key opinion leaders, advisory boards, patient advocacy groups) and internal partners across Research, Global Medical Affairs, and Marketing. Demonstrated track record across leadership roles, including work with senior clinical development staff and established credibility with external collaborators such as opinion leaders and regulators.
Medical Director, Clinical Development, Endocrinology Regeneron PharmaceuticalsMedical Director, Clinical Development, EndocrinologyTarrytown, NY$284,900–$385,700 / yearIn this role, you will serve as Medical Lead for clinical trials and are responsible for the design of clinical study concepts leading to clinical trial protocols and oversight of studies, while collaborating with cross-functional stakeholders. This role requires a high-performing and highly passionate physician scientist who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to clinical research.
Medical Director, Clinical Development, Obesity Regeneron PharmaceuticalsMedical Director, Clinical Development, ObesityTarrytown, NY$284,900–$385,700 / yearIn this role, you will serve as Medical Lead for clinical trials and are responsible for the design of clinical study concepts leading to clinical trial protocols and oversight of studies, while collaborating with cross-functional stakeholders. This role requires a high-performing and highly passionate physician scientist who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to clinical research.
Clinical Research Coordinator The Geneva FoundationClinical Research CoordinatorWest Point, New YorkHeadquartered at the Uniformed Services University of the Health Sciences (USU), MIRROR provides coordination and support of inter-service and inter-disciplinary partnerships across military treatment facilities (MTFs), military training centers (MTCs), and civilian academic centers to execute cutting-edge research in order to mitigate the burden of MSI on military readiness. Maintain and update files of all applicable regulatory documentation for IACUC or IRB (including protocols, approvals, amendments, modifications, etc.) as well as any communications with the sponsor or any other Federal or regulatory office (including prior approvals, change in scope, etc.).
NewPharmD Program Associate - Clinical Operations & Program Management Regeneron Pharmaceuticals IncPharmD Program Associate - Clinical Operations & Program Managementtarrytown, NY$98,100–$160,100 / yearAssignments in this 2-year development program will expose candidates to critical issues and decision-making processes, acquire high-level knowledge of the business and department operations, and gain hands-on work experience in different areas. Clinical Operations & Program Management - Associates will support the management of clinical trials by actively contributing to key activities related to trial set-up, execution, conduct and close out.
NewPharmd Program Associate - Clinical Operations & Program Management Regeneron PharmaceuticalsPharmd Program Associate - Clinical Operations & Program ManagementTarrytown, NY$98,100–$160,100 / yearAssignments in this 2-year development program will expose candidates to critical issues and decision-making processes, acquire high-level knowledge of the business and department operations, and gain hands-on work experience in different areas. Clinical Operations & Program Management - Associates will support the management of clinical trials by actively contributing to key activities related to trial set-up, execution, conduct and close out.
Principal Product Manager, Admin & Clinical Workflows Butterfly NetworkPrincipal Product Manager, Admin & Clinical WorkflowsNew City, NYDrive product development for administrator-facing features like Proficiency Management, Analytics, Program Performance, User Management and Access Roles, Fleet Management, Butterfly Academy & Education Dashboard — ensuring health system administrators have a seamless, efficient experience managing their POCUS programs. Lead cloud-based clinical workflow products such as Documentation (Worksheets, Tags, Exam Types), and Quality Assurance tools — translating clinician needs into intuitive, simple,reliable tools that fit into existing care delivery workflows.
NewPharmd Program Associate - Clinical Sciences Regeneron PharmaceuticalsPharmd Program Associate - Clinical SciencesTarrytown, NY$98,100–$160,100 / yearAssignments in this 2-year development program will expose candidates to critical issues and decision-making processes, acquire high-level knowledge of the business and department operations, and gain hands-on work experience in different areas. Clinical Sciences: Associate will participate in clinical activities throughout the lifetime of a drug development program, driving development programs from pre-IND/IND stage through completion of pivotal trials.
NewPharmD Program Associate - Clinical Sciences Regeneron Pharmaceuticals IncPharmD Program Associate - Clinical Sciencestarrytown, NY$98,100–$160,100 / yearAssignments in this 2-year development program will expose candidates to critical issues and decision-making processes, acquire high-level knowledge of the business and department operations, and gain hands-on work experience in different areas. Clinical Sciences: Associate will participate in clinical activities throughout the lifetime of a drug development program, driving development programs from pre-IND/IND stage through completion of pivotal trials.
Medical Director, Clinical Development, Oncology (Lung, Breast, Colorectal, Gastric Cancers) Regeneron PharmaceuticalsMedical Director, Clinical Development, Oncology (Lung, Breast, Colorectal, Gastric Cancers)Tarrytown, NY$284,900–$385,700 / yearIn this role, you will design clinical study concepts, oversee the medical and scientific integrity of clinical trials, and ensure patient safety across trial activities while collaborating with the Global Clinical Study Team and key investigators. We are seeking a Medical Director, Clinical Development to join our Oncology team, supporting solid tumor drug development on-site in Tarrytown, NY or Warren, NJ.