Scientist/Sr. Scientist, Clinical Pharmacology SystImmune, Inc.Scientist/Sr. Scientist, Clinical PharmacologyPrinceton, NJ$90,000–$140,000 / yearResponsible for Pharmacometrics development, PK and PK/PD analysis, and documentation: Conduct modeling and simulation work on PopPK, ER, PK/PD or exploratory analyses and guides PK/PD modeling or simulations as appropriate and to guide study design, inform dose selection and optimization, and efficacy/safety assessments. Responsible for clinical development strategy, clinical study design/protocol development, and documentation from CP perspective in the assigned project(s): Contributes to clinical development strategies of pipeline products across various therapeutic areas and design of clinical studies with some supervision under supervision.
Scientist/Sr. Scientist, Clinical Pharmacology Systimmune IncScientist/Sr. Scientist, Clinical PharmacologyPrinceton, NJ$90,000–$140,000 / yearResponsible for Pharmacometrics development, PK and PK/PD analysis, and documentation: Conduct modeling and simulation work on PopPK, ER, PK/PD or exploratory analyses and guides PK/PD modeling or simulations as appropriate and to guide study design, inform dose selection and optimization, and efficacy/safety assessments. Responsible for clinical development strategy, clinical study design/protocol development, and documentation from CP perspective in the assigned project(s): Contributes to clinical development strategies of pipeline products across various therapeutic areas and design of clinical studies with some supervision under supervision.
Project Manager Columbia UniversityProject ManagerNew York, NYResponsibilities will include general project management and coordination; Institutional Review Board (IRB) submissions, amendments, and reporting related to the protection of human subjects in research; data assembly, database management, data quality control, and guided data analyses; report generation; and potential co-authorship on published studies. In addition, the Project Manager will contribute to scholarly dissemination by supporting abstract, presentation, and manuscript development; coordinating multi-author writing and revision workflows; and providing editorial coordination for complex research products, including manuscripts, reports, conference materials, and other dissemination products.
Robotics Clinical Sr Sales Rep Zimmer Biomet Holdings IncRobotics Clinical Sr Sales RepNew York City, NY$100,000–$120,000 / yearPartners with Technology Solutions Manager and Field Service technicians to onboard new accounts, including attend system installation, provide in-service to relevant facility staff, train local implant sales colleagues and provide clinical support during enabling technology cases. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards.
Program Lead, Clinical Research NYU Langone Medical CenterProgram 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 Associate Alto Neuroscience IncClinical Research AssociateNYRemote$80,000–$125,000 / yearDetermine whether all adverse events (AEs) are appropriately reported within the time periods required by GCP, the protocol, the Ethic Committees (IRB/IEC), Sponsor and the applicable regulatory requirement(s) Ensure deviations from the protocol, SOPs, GCP, and the applicable regulatory requirements are documented and communicated appropriately and take appropriate action to prevent recurrence of the detected deviations. The Clinical Research Associate (CRA) is responsible for the oversight of assigned investigative sites in accordance with all applicable protocols, project plans, Sponsor SOPs, GCP guidelines, and regulatory requirements from site initiation through site close out.
Regional RN Clinical Manager Community OptionsRegional RN Clinical ManagerEdison, New JerseyCommunity Options, Inc. is a national non-profit agency providing residential group home, day habilitation and supported employment services to individuals with intellectual and developmental disabilities in 12 states. The Regional RN Clinical Manager provides clinical leadership, oversight, and support to Registered Nurses (RNs) and Licensed Practical Nurses (LPNs) across multiple service regions.
Enterprise Account Manager - Northeast Ambry Genetics CorpEnterprise Account Manager - NortheastTrenton, NJCollaborating peers include but are not limited to Account Executives, Area Sales Directors, Field Implementation Managers, Technical Implementation Managers, IT, Software Development, Enterprise Solutions Executives, Enterprise Sales Directors, Marketing and Genetic Science Liaisons. An Account Manager is expected to be able to lead the overall client governance and build strong relationships with the operational leaders, including ESE's, Digital Health Opps, VP and C-Suite executives, that strengthen Ambry's position to drive change, solve issues, and retain and expand Ambry's business with the customer.
Manager of Clinical Appeals and Grievances HealthfirstManager of Clinical Appeals and GrievancesNJ$103,400–$149,430 / yearProvides guidance in the preparation of case preparation for Medical Director Review ensuring that all pertinent information (i.e. case summary, contract information, internal and external responses, diagnosis, and CPT codes and descriptions) has been obtained during investigation and is presented as part of the case. If you have a disability under the Americans with Disability Act or a similar law and want a reasonable accommodation to assist with your job search or application for employment, please contact us by sending an email to careers@Healthfirst.org or calling 212-519-1798.
CS - Research Assistant - Cardiology Columbia UniversityCS - Research Assistant - CardiologyNew York, NYThe research assistant will also collaborate with physician investigators, research fellows, clinical research coordinators, a research manager, a regulatory manager, and a data manager as part of HFRI's multidisciplinary research infrastructure. This position provides MS or PhD students in biostatistics or related quantitative disciplines with the opportunity to contribute to investigator-initiated clinical research focused on improving outcomes in patients with heart failure.
Clinical Terminologist TempusClinical TerminologistNew York City, NY$67,000–$95,000 / yearTempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time. Responsibilities: Collaborate with cross-functional teams to manage and update terminology services made available across the company.
Senior Manager, Clinical Operations - GI Iterative HealthSenior Manager, Clinical Operations - GINew York, NY$140,000–$165,000 / yearAs the Senior Manager, Clinical Operations- GI at Iterative Health you will serve as a strategic advisor to sponsors, CROs, and research sites, translating operational challenges into scalable solutions that improve study execution, accelerate activation timelines, and drive patient recruitment performance. By combining deep clinical research expertise with a consultative approach, this individual will help strengthen sponsor relationships, elevate site performance across the network, and contribute directly to Iterative Health's mission of bringing innovative therapies to patients faster.
NewProgram Lead II, Clinical Program Development AbbVie, IncProgram Lead II, Clinical Program DevelopmentBranchburg, NJResponsible for developing, managing, mentoring clinical operations (direct and indirect) staff to enable growth into leadership roles, including strategic leadership and direct supervision of 4 - 15 study manager(s) and up to 30 indirect staff, career development of clinical operations staff and creating an inclusive, innovative and learning environment where staff and studies/programs will succeed. In alignment with the asset's strategy and incorporating the science and the operations, develops the clinical operational strategy and is responsible for the execution of clinical studies/programs (e.g., generation of operational timelines, enrollment options, assessment of availability of the patient population, balancing complexity of trial designs vs speed).
Asst Dir, Clin Res Solutions Columbia UniversityAsst Dir, Clin Res SolutionsNew York, NY$125,000–$150,000 / yearReporting to the Director, Clinical Research Initiatives in the Irving Institute for Clinical and Translational Research, the Assistant Director operates with a high degree of independence and accountability, translating strategic priorities into executable plans while ensuring regulatory-compliant, high-quality operational workflows and solutions in support of research. Coordinate with cross-departmental and external stakeholders to support clinical research solutions that interface with Epic, such as EDC systems, REDCap, and Clinical Trial Management Systems, and manage full project execution-including planning, stakeholder engagement, and risk management-in partnership with Irving Institute leadership and investigators.
Senior Manager, Global Clinical Regulatory Lead PTC TherapeuticsSenior Manager, Global Clinical Regulatory LeadWarren, NJ$130,000–$164,600 / yearJob Description Summary: The Senior Manager, Global Clinical Regulatory Lead, is responsible for providing strategic and operational direction for the planning, management, support and execution of regulatory activities for PTC drug products (clinical and commercial) within the US as applicable. Clinical Trial Applications (CTAs): Initiate and execute CTA/CTNs in US, EU, and globally by keeping up to date with regulations and critically analyzing the interactions with health authorities to ensure that any outstanding issues are addressed.
Clinical Research Associate CareerscapeClinical Research AssociateMorristown, NJ$78,000–$98,000 / yearFull timeOur client, a pharmaceutical company based in Morristown, New Jersey, is hiring a Clinical Research Associate to oversee clinical trial activities across multiple study sites. This position works closely with investigators, site coordinators, and internal study teams to keep trials on schedule and in compliance with FDA regulations.
Youth Residential Clinical Supervisor Woods ServicesYouth Residential Clinical SupervisorMount Holly, New JerseyRemoteThis continuum is designed to meet the complex needs of each individual and creates a continuum of services that are able to meet the needs of children, adults, and families through a continuum of services utilizing an integrated care model. Legacy Treatment Services is a vibrant nonprofit behavioral health organization that utilizes cutting-edge technology and evidence-based practice in treatment and clinical care.
Department Administrator Rutgers The State University of New JerseyDepartment AdministratorNew Brunswick, NJUnder Policy 100.3.1 Immunization Policy for Covered Individuals, if employment will commence during Flu Season, Rutgers University may require certain prospective employees to provide proof that they are vaccinated against Seasonal Influenza for the current Flu Season, unless the University has granted the individual a medical or religious exemption. With its broad and multidisciplinary faculty expertise, the Environmental and Occupational Health Sciences Institute (EOHSI) is an international resource that supports basic and clinical research in environmental health sciences and exposure assessment and fosters associated programs in environmental health education and public policy.
Global Clinical Study Senior Manager BeOne Medicines AGGlobal Clinical Study Senior ManagerNY$136,400–$181,400 / yearEnsures that the clinical study is operationally feasible in all regions, drives trial feasibility, country allocation and site selection process for assigned region in collaboration with feasibility managers, country heads, medical affairs and any other stakeholders. This role serves as the primary global operational owner, responsible for aligning cross-functional stakeholders, managing global study strategy execution, and driving performance against timelines, quality, and budget.
Clinical Trial Manager - Investigator Initiated Studies Heartflow IncClinical Trial Manager - Investigator Initiated StudiesNew York, NY$90,000–$130,000 / yearHeartflow is the first AI-driven non-invasive integrated heart care solution across the CCTA pathway that helps clinicians identify stenoses in the coronary arteries (RoadMapAnalysis), assess coronary blood flow (FFRCT Analysis), and characterize and quantify coronary atherosclerosis (Plaque Analysis). The flagship product-an AI-driven, non-invasive cardiac test supported by the ACC/AHA Chest Pain Guidelines called the Heartflow FFRCT Analysis-provides a color-coded, 3D model of a patient's coronary arteries indicating the impact blockages have on blood flow to the heart.