Strategic Initiatives Manager-Venture, Innovation and Growth Memorial Sloan Kettering Cancer CenterStrategic Initiatives Manager-Venture, Innovation and GrowthNY$92,700–$148,400 / yearThe Strategic Initiatives Manager-Venture, Innovation and Growth serves as a partner in project execution within MSK's Strategy & Growth division and will operate across a dynamic portfolio of innovation, commercialization, operational and venture development activities. Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it.
Associate Strategic Initiatives Manager-Venture, Innovation and Growth Memorial Sloan Kettering Cancer CenterAssociate Strategic Initiatives Manager-Venture, Innovation and GrowthNew York, New YorkThe Associate Strategic Initiatives Manager-Venture, Innovation and Growth serves as a partner in project execution within MSK’s Strategy & Growth division and will operate across a dynamic portfolio of innovation, commercialization, operational and venture development activities. Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it.
NewBusiness Operations Associate Integrated Resources, IncBusiness Operations AssociateFlorham Park, New JerseyContractorJob Description• Procurement and Budget Tracking.• Prepare and process all purchase orders, invoices, and other payments (within 72 hours of receipts) and reconcile departmental expenses when problems arise (initiate request for resolutions with 72 hours of identification).• Maintain tracking system for all payments that flow though the U.S.• Obtain actual and prepare spending reports (after the close of each accounting periods as requested by manager for global group).• Coordinate the compilation, distribution and storage of all departmental legal agreements and related U.S.-routed documents utilizing Ariba contracts and update all (global) post-agreement records via tracking documents and POMS.• Coordinate the entry of all CDAS agreements into Ariba contracts, POMS, and our master agreement list.
Clinical Team Manager (RN), Hospice Home Care, Queens VNS HealthClinical Team Manager (RN), Hospice Home Care, QueensLong Island City, NY$98,200–$130,800We’re one of the largest nonprofit home- and community-based health care organizations in the country, and today, more than 11,500 team members work together to make a difference in the lives of more than 99,000 patients and members on any given day. Participates in Hospice Team meetings, IDG management meetings, and serves on relevant committees for the purposes of information exchange, team collaboration, development of procedures and documentation tools, development of quality and training.
NewClinical Supervisor Mitchell MartinClinical SupervisorQueens, NY$70,000–$80,000 / yearBy applying for this job, you agree to receive AI-generated calls, text messages, and/or emails from Mitchell Martin Inc and its affiliates and contracted partners at various frequency through traditional and automated methods. Clinical Supervisor - Astoria, NY (Onsite) - Full Time - Mon-Fri 08:30am-05:00pm (1 Late Evening) - $70,000-$80,000 Per Year.
Senior Clinical Research Associate I Zp Group LlcSenior Clinical Research Associate INYRemote$115,000–$125,000 / yearKeywords: clinical research, clinical trials, CRA, GCP, ICH, regulatory compliance, site monitoring, clinical monitoring, CTMS, EDC, cardiovascular studies, CNS trials, diabetes research, GLP-1, site management, FDA regulations, clinical operations, documentation, quality assurance, protocol compliance, investigator sites, patient safety, clinical development. Piper Companies is seeking a Senior Clinical Research Associate I to join a global organization within the clinical research and life sciences industry for a remote permanent role with 60-75% travel to sites in the US.
NewMedical Writer Integrated Resources, IncMedical WriterMadison, New JerseyContractorEnsure key messages and document style are communicated to authors and team to ensure consistency across different documentsTechnical Skill Requirements:Able to work well in cross-functional teams, exhibiting a combination of active listening skills and also the confidence to guide decision-making for the document content strategy. Collaborate with development Product Teams to prepare or lead preparation of Clinical/Regulatory documents (MD deliverables).Identify resource, timeline and emerging data interpretation issues that have regulatory impact, and clearly communicate the consequences of these issues to the project team and line management.
Senior Data Analyst Northwell Health IncSenior Data AnalystNew Hyde Park, NYPrepares support documents and presents project deliverables; identifies and communicates project needs and issues to appropriate leadership; coordinates initiatives, follows-up on outstanding issues and partners with the leadership and other departments, as necessary. When determining a team members base salary and/or rate, several factors may be considered as applicable (e.g., location, specialty, service line, years of relevant experience, education, credentials, negotiated contracts, budget and internal equity).
NewSystem Manager, Respiratory Sleep Lab Westchester Medical Center Health NetworkSystem Manager, Respiratory Sleep LabNY$47.64–$60.30 / hourJob Category Job Category Advanced Clincial Providers Advanced Practice Providers Allied Health Prof/Technical Clerical/Administrative Support Executive/Management Finance/Info Systems Nursing Support Nursing/Nursing Management Physicians Professional/Non-Clinical Service/Trades. Good Samaritan Hospital in Suffern, NY, is a 286-bed hospital providing emergency, medical, surgical, obstetrical/gynecological and acute-care services to residents of Rockland and southern Orange counties in New York; and northern Bergen County, NJ.
Head of Operations SomethingsHead of OperationsNew York City, New YorkThe work is high agency, high craft, and high impact: You will run the day-to-day delivery operation that connects thousands of struggling teens to certified peer mentors and build the operational backbone that lets us do it for many more, in more states, at a higher bar, every quarter. 10+ years of operations experience in healthcare or digital health, including owning and running a provider / care-delivery operation that has scaled — not just being at a company that scaled, and not a purely corporate or G&A ops function.
Sr. Clinical Specialist, Surgical Operations (Northeast) Aspen Neuroscience IncSr. Clinical Specialist, Surgical Operations (Northeast)New York, NY$136,800–$167,200 / yearExperience supporting early-phase or first-in-human studies, MRI-guided workflows, or advanced therapy delivery (cell or gene therapy), and contributing to development of field procedures, training programs, or site readiness processes. Minimum of 10 years of progressively responsible experience in field clinical support, surgical support, clinical applications, or trial-facing procedural roles within complex, procedure driven environments (e.g., neurosurgery, implantable therapies, image-guided interventions).
Clinical Research Associate - Sponsor Dedicated IQVIAClinical Research Associate - Sponsor DedicatedParsippany, KansasEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Senior Contracts and Budget Associate - FSP Precision Medicine Group LLCSenior Contracts and Budget Associate - FSPNYRemote$68,700–$103,100 / yearPosition Summary: Review, draft, negotiate and track a variety of legal agreements including confidentiality disclosure agreements (CDA), initial clinical trial agreements (CTA), amendments to the clinical trial agreements (CTA-A), site budgets and other various types of documents. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs.
Emergency and Trauma Center Operations Technician - Full Time - Day Hackensack Meridian HealthEmergency and Trauma Center Operations Technician - Full Time - DayHackensack, New JerseyFull timeThe Emergency & Trauma Center Operations Technician will work under the management of the ETC Operations Manager and is responsible for maintaining the operational needs of the department including customer service, transportation, supplies, equipment and environmental service needs. The posted rate of pay in this job posting is a reasonable good faith estimate of the minimum base pay for this role at the time of posting in accordance with the New Jersey Pay Transparency Act and does not reflect the full value of our market-competitive total rewards package.
Operations Manager - New Rochelle/Park Care Sun River Health IncOperations Manager - New Rochelle/Park CareYonkers, NY$66,300–$82,875 / yearResponsible for the successful management of health center operations, including but not limited to the supervision of non-clinical staff, creates and reviews analytical data reports, coordinates maintenance requests, interacts with patients and offers assistance as needed, and orders all necessary supplies and equipment. Sun River Health provides the highest quality of comprehensive primary, preventative and behavioral health services to all who seek it, regardless of insurance status and ability to pay, especially for the underserved and vulnerable.
Emergency & Trauma Center Operations Technician - Full Time - Night Hackensack Meridian HealthEmergency & Trauma Center Operations Technician - Full Time - NightHackensack, New JerseyFull timeThe Emergency & Trauma Center Operations Technician will work under the management of the ETC Operations Manager and is responsible for maintaining the operational needs of the department including customer service, transportation, supplies, equipment and environmental service needs. The posted rate of pay in this job posting is a reasonable good faith estimate of the minimum base pay for this role at the time of posting in accordance with the New Jersey Pay Transparency Act and does not reflect the full value of our market-competitive total rewards package.
Emergency and Trauma Center Operations Technician - Part Time - Day Hackensack Meridian HealthEmergency and Trauma Center Operations Technician - Part Time - DayHackensack, New JerseyThe Emergency & Trauma Center Operations Technician will work under the management of the ETC Operations Manager and is responsible for maintaining the operational needs of the department including customer service, transportation, supplies, equipment and environmental service needs. The posted rate of pay in this job posting is a reasonable good faith estimate of the minimum base pay for this role at the time of posting in accordance with the New Jersey Pay Transparency Act and does not reflect the full value of our market-competitive total rewards package.
Emergency Trauma Center Operations Technician - Full Time - Evening Hackensack Meridian HealthEmergency Trauma Center Operations Technician - Full Time - EveningHackensack, New JerseyFull timeThe Emergency & Trauma Center Operations Technician will work under the management of the ETC Operations Manager and is responsible for maintaining the operational needs of the department including customer service, transportation, supplies, equipment and environmental service needs. The posted rate of pay in this job posting is a reasonable good faith estimate of the minimum base pay for this role at the time of posting in accordance with the New Jersey Pay Transparency Act and does not reflect the full value of our market-competitive total rewards package.
Sr. Manager, Patient Experience Privia Health Group, IncSr. Manager, Patient ExperienceNY$80,000–$100,000 / yearThe Privia Platform is led by top industry talent and exceptional physician leadership, and consists of scalable operations and end-to-end, cloud-based technology that reduces unnecessary healthcare costs, achieves better outcomes, and improves the health of patients and the well-being of providers. ?Technical Requirements (for remote workers only, not applicable for onsite/in office work): In order to successfully work remotely, supporting our patients and providers, we require a minimum of 5 MBPS for Download Speed and 3 MBPS for the Upload Speed.
Clinical Informatics Specialist Richmond Medical CenterClinical Informatics SpecialistStaten Island, New YorkThis role is responsible for the design, optimization, governance, and sustainment of clinical workflows and electronic health record (EHR) solutions to support patient safety, regulatory compliance, quality outcomes, and efficient clinical operations. · Build, maintain, and support clinical content including order sets, documentation templates, clinical decision support (CDS), alerts, and workflows.
Director of Clinical Services - Supportive Housing URI CareersDirector of Clinical Services - Supportive HousingNew York, New YorkThe Director, Clinical Services collaborates closely with Case Managers, Housing Specialists, the Economic Empowerment Specialist, Operations leadership, and external clinical partners to ensure services reflect best practices in supportive housing, domestic violence recovery, and family stabilization. In addition to emergency and transitional housing, URI delivers a robust continuum of Justice Initiatives—including economic empowerment, legal education and advocacy, prevention and youth programming, and abusive partner intervention—designed to break cycles of violence, instability, and poverty.
Director, Privacy Counsel Omada Health IncDirector, Privacy CounselNY$242,880–$303,600 / yearThis individual contributor role will operate at the intersection of healthcare regulatory law, consumer technology, and clinical operations, providing practical, business-oriented guidance that enables innovation while protecting our members' data and trust. You bring 8+ years of privacy law experience, including meaningful in-house experience at a healthcare, digital health, or life sciences company and/or at a top-tier law firm counseling healthcare, digital health, and/or life sciences clients.
Assistant Nurse Manager CareWell HealthAssistant Nurse ManagerEast Orange, NJThis position also supports the Nurse Manager’s operational leadership functions including staffing coordination, payroll validation, scheduling oversight, chart quality review, staff counseling, policy development, interview participation, and patient experience initiatives. In collaboration with physicians, nursing leadership, and the interdisciplinary team, the ANM assists in identifying at-risk patients, coordinating care plans, and ensuring optimal patient outcomes.
Senior Director, Clinical Pharmacology PTC Therapeutics IncSenior Director, Clinical PharmacologyNJ$237,400–$298,900 / yearThis includes performing, coordinating, and overseeing PK & PK/PD assessment(s) in patients; interpreting data; and providing timely Clinical Pharmacology-related support to various functions, including, but not limited to, clinical, biostatistics, medical writing, regulatory, commercial, toxicology, preclinical pharmacology, discovery research as well as external Contract Research Organizations (CROs). D. or equivalent academic training in pharmacokinetics, pharmaceutical sciences or a related discipline and a minimum of 9 years of relevant and progressively responsible experience in clinical pharmacology including extensive experience in DMPK in a pharmaceutical, biotechnology or related environment OR equivalent experience and/or education.
Director, Global Procurement - Marketing Operations Merck & Co IncDirector, Global Procurement - Marketing OperationsRahway, NJ$156,900–$247,000 / yearTypical Activities: Contract review/negotiations; PO issue resolution; creation of new vendors; supplier issue resolution; technology/process execution; dialogues and meetings with Global Procurement in connection with supplier and stakeholder resolution; data gathering and analysis leading to short/medium term insights not in connection with Sourcing Management Process or strategy creation/execution; all transactions not in connection with Sourcing Management Process or strategy creation/execution which ensure sustainability of the procurement function. Responsibilities: This role is responsible and accountable for sustaining existing and developing new cooperation frameworks across three stakeholder groups: With Procurement Colleagues: Participates/leads teams of global, regional & local representatives to develop and implement strategic source plans as well as to ensure alignment on key initiatives and priorities for broader Marketing services categories.
Clinical Research Administrative Assistant Frontage Clinical Services IncClinical Research Administrative AssistantSecaucus, NJ$20–$22 / hourOur core competencies include pre-clinical, drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials. Position Summary: We are seeking a proactive and detail-oriented Clinical Research Assistant to provide critical administrative and operational support within our research environment.
Chair, Radiology New York Medical CollegeChair, RadiologyValhalla, New YorkPart timeEnsure an academically robust and fully accredited Graduate Medical Education (GME) Program supported by a dedicated, professional teaching faculty that is welcoming to learners, and is overseen by knowledgeable program directors that represent and uphold the SOM educational mission, working collaboratively with the SOM designated institutional official and the Dean of GME as appropriate. Ensure that the Department remains current with all payments to NYMC for services and benefits provided by the SOM, including CME fees, Faculty Deans Dues, charges for the support of residents conducting research, fees for biostatistical support services for research, etc., as applicable.
Healthcare Systems Implementation Project Manager RSM US LLPHealthcare Systems Implementation Project ManagerNew York, NY$95,400–$192,000 / yearAs a member of the RSM's National Healthcare consulting practice, you will join professionals with a broad knowledge of the Healthcare industry including: financial analysis and revenue cycle management, clinical operations, regulatory reporting and compliance, HIPAA privacy, security, and Healthcare IT. Support the implementation of leading packaged software solutions that have been developed to accommodate healthcare business and management processes, regulatory requirements and other business needs such as: Epic, Meditech, Cerner, and Solventum (3M).
Executive Director, Product Development Team Leader, Clinical Research, Hematology - Lymphoma Merck & Co IncExecutive Director, Product Development Team Leader, Clinical Research, Hematology - LymphomaNJ$310,900–$489,400 / yearWorking closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects, and assist the Associate Vice President and/or Vice President in ensuring that appropriate Corporate personnel are informed of the progress of studies of our company and competitors' drugs, and of internal and external expert opinion on scientific questions relevant to their areas of responsibility. Leading internal governance presentations to senior management and committees, communicating progress and key changes in product development strategy between stage gates, ensuring early alignment with line management, and facilitating issue escalation and cross-functional collaboration as needed for governance approval.
NewClinical Research Coordinator - Raleigh, NC IQVIAClinical Research Coordinator - Raleigh, NCParsippany, North CarolinaThe ideal candidate has hands-on clinical research experience, is comfortable performing study-related procedures, and possesses strong organizational skills in both data management and regulatory documentation. Experience supporting regulatory processes , including electronic regulatory filing, document maintenance, and ensuring study documentation complies with sponsor and regulatory requirements.
CRM Practice Lead IQVIACRM Practice LeadParsippany, New JerseyThis role will focus on enabling effective, scalable, and consistent sales execution through platforms and capabilities such as CRM, Sales Enablement, account planning, opportunity management, pipeline management, forecasting, sales content, reporting, and related commercial technologies. • Lead discovery and intake activities with sales leaders, commercial operations, regional stakeholders, and end users to identify opportunities to improve sales productivity, process consistency, data quality, and platform adoption.
Manager Clinical Supply Chain - Operations Alnylam Pharmaceuticals IncManager Clinical Supply Chain - OperationsNY$122,400–$165,600 / yearYou will partner closely with cross-functional teams including Clinical Operations, Quality Assurance, Regulatory Affairs, and external vendors to execute clinical trials effectively. In this position, you will play a pivotal role in ensuring reliable, compliant execution of clinical supply across programs, supporting Alnylam's growing pipeline and patient needs.
NewSupervisor, Clinical Laboratory Operations Northwell Health IncSupervisor, Clinical Laboratory OperationsNYWhen determining a team members base salary and/or rate, several factors may be considered as applicable (e.g., location, specialty, service line, years of relevant experience, education, credentials, negotiated contracts, budget and internal equity). a fast-paced environment by providing operational leadership and by interacting with clients, presenting organizational capabilities, defining scope of work and delivering results through.
NewSenior Clinical Systems Programmer (JReview), Data Operations Integrated Resources, IncSenior Clinical Systems Programmer (JReview), Data OperationsWoodcliff Lake, New JerseyFull timeStrong SAS programming skills in Windows and UNIX environment, with proficiency in SAS/Base, SAS Macros, SAS/Graph, SAS/AF, SQL; • Strong JReview skills in terms of program development, administration, maintenance, and user support; • Extensive experience of handling external data, e.g., laboratory data, PK, ECG,Tumor, etc. • Design and develop macros, applications, and other utilities to expedite programming activities and usage by the Oncology Data Management and other areas of Clinical for data review.
NewSenior 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.
NewClinical Supply Manager Integrated Resources, IncClinical Supply ManagerJersey City, New JerseyContractorExperience with the following clinical supply demand management tools are highly preferred: TC, IVR/IWR/IRT, Forecasting and Simulation, Optimizer, IVRS, and SAP.• Experience with any or all of the following functions or processes are highly preferred: S&OP, clinical supply pack/label/distribution, clinical trial operations, project management, pharma/bio research and development, and inventory management.• Job DescriptionQualifications• A minimum of a Bachelor's Degree and 4 years of experience in clinical supplies or a related supply chain role (supply or demand planning) is required OR a minimum of 8 years of experience in clinical supplies or a related supply chain role is required.•
NewDirector, IT Network Operations --FULLTIME Integrated Resources, IncDirector, IT Network Operations --FULLTIMENewark, New JerseyFull timeAn advanced degree is a plus, preferably in Engineering or Science10 plus years prior IT Network/Telecom related work experience Additional licensing, certifications, registrations:Data Network certifications (CCNP or CCNA) requiredMCSE (Microsoft Certified System Engineer) requiredTelephone PBX System certification preferred • ITIL certification preferredQualificationsSkills and Abilities:Requires exceptional analytical thinking skillsRequires excellent verbal and written communication skillsRequires excellent interpersonal skills and the ability to work effectively with others as a teamRequires having managed a budget of $10+ millionRequires having managed a blended team of full time employees and contractors (about 30 total)Travel (If Applicable): There will be travel from time to time within the state of NJ. Responsible for development and management of network strategies and initiatives that take advantage of existing technologies as well as bring new technologies to ensure that all data is protected and available to appropriate systems, applications, and customers in an efficient mannerManage the overall Disaster Recovery plans for the voice and data network to meet business, legal and regulatory requirements.
NewClinical Research Associate Integrated Resources, IncClinical Research AssociateSouth Plainfield, New JerseyFull timeRequirements:Support project management oversight of Clinical Development activities for multiple domestic and international trials, including:Track study timelinesReview and track study budgetsProvide periodic updates on Clinical DevelopmentGradually develop responsibilities for management of contract research organization (CROs) activities for clinical and data managementProvide monitoring support, in some cases functioning as the primary site monitor. Qualifications• Thorough knowledge of Good Clinical Practice, clinical trial design, regulatory processes, and global clinical development process.• 3-5 years of investigative site monitoring or study coordinator/study nurse experience.• Hands-on experience in data cleaning and analysis required.•
NewSenior Clinical Trial Associate Sarepta Therapeutics IncSenior Clinical Trial AssociateNJ$107,200–$134,000 / yearThe salary offer is commensurate with Sarepta's compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity. Coordinates and tracks the distribution and subsequent retrieval of clinical documents, including but not limited to protocols, protocol amendments, IBs, ICF's, monitoring visit reports, etc.
Anatomic Pathology Operations Manager MRINetwork JobsAnatomic Pathology Operations ManagerPleasantville, New YorkJob Summary: The Anatomic Pathology Operations Manager is responsible for coordinating and reviewing all activities of the histology, cytology, and MOHS laboratories to achieve maximum quality of testing and compliance with all requirements by regulatory agencies. Any hazardous chemicals the employee may be exposed to are listed in the hospital’s SDS (Safety Data Sheet) data base and may be accessed through the hospital’s Intranet site (Employee Tools/SDS Access).
Clinical Research Associate II, Oncology Pharmaron Beijing Co LtdClinical Research Associate II, OncologyNYRemote$90,000–$100,000 / yearWhat We are Looking for: Bachelor's degree, RN, or equivalent combination of education and relevant experience; life sciences background preferred 3+ years of clinical monitoring experience within sponsor, CRO, or investigative site environments Hands-on oncology monitoring experience required, including Phase I studies Strong knowledge of ICH-GCP guidelines and applicable regulatory requirements Ability and willingness to travel up to 30% based on study needs Excellent organizational skills with strong attention to detail Strong communication skills and ability to manage site relationships effectively Experience using CTMS, EDC, eTMF, and other clinical trial systems Experience in early-phase startup environments Ability to independently prioritize workload across multiple sites and studies Why Pharmaron? Position: Clinical Research Associate II, Oncology Location: Remote (East Coast USA Preferred) Salary: $90,000 to $100,000 D.O.E Unfortunately, we cannot support work visa permit applications for this role About Pharmaron Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life.
Senior Associate, People Operations & Early Career Programs Roivant Sciences IncSenior Associate, People Operations & Early Career ProgramsNew York, NY$110,000–$130,000 / yearSince its inception in 2014, Roivant has achieved the following critical milestones in support of its vision: built over 20 Vants; 12 consecutive positive Phase 3 trials; 8 FDA approvals; 5 successful IPOs; >$6B in capital raised; >$10B in global pharma partnerships and proceeds; and continued pipeline expansion across various modalities and therapeutic areas through in-licensing and acquisition of novel product candidates and technology platforms. Position Summary: This role sits at the intersection of people operations and early career program management, owning both the day-to-day execution of people operations activities across Roivant and its portfolio companies and the strategic design and delivery of our early career talent programs.
Deputy Director of Pharmacy Operations Metroplus Health Plan IncDeputy Director of Pharmacy OperationsNew York, NY$175,000–$183,909 / yearAdditionally, this position is responsible for ensuring fraud, waste and abuse risks are identified and addressed through internal monitoring and partnering with the PBM, MPH Special Investigation Unit (SIU) and oversight of the Restricted Recipient Program (RRP). This position engages with senior leaders and key stakeholders to ensure the optimal utilization of technology and resources, to support the implementation of enterprise-wide pharmacy systems and processes, including large-scale operational projects.
NewCustomer Site Operations Technician Azenta IncCustomer Site Operations TechnicianSouth Plainfield, NJ$22–$28 / hourDatabase entry into Watson LIMS, POLARIS, LabMatrix IT systems, and REES (with potential for other databases as well) in order to support normal Specimen Library operations and study design changes needed due to protocol amendments. Serve as a REES On-call tech a minimum of 1 week per month in the event of temperature excursions planned or otherwise Initiate communication with multiple contacts within customer site to maintain or cultivate relationships and gather intelligence about customers' needs and problems.
Clinic Manager - Hyperbaric Medicine & Practice Operations MD HyperbaricClinic Manager - Hyperbaric Medicine & Practice OperationsManhasset, NYAs our Manhasset location expands its insurance-based offerings, we are seeking a highly organized and detail-oriented leader with experience in medical practice operations, insurance verification, authorizations, patient financial coordination, and healthcare administration. We are seeking a hands-on Clinic Manager with a strong clinical background (e.g., MA, EMT, RN, LPN, Practice Manager, or similar) to own and operate the day-to-day performance of our hyperbaric oxygen therapy (HBOT) center.
Maintenance Operations Coordinator MedsMaintenance Operations CoordinatorElmhurst, New YorkSupply Chain & Inventory Control Inventory Management: Monitor levels of non-medical supplies (packaging, cleaning agents, lab consumables) and place orders to ensure zero stock-outs. Preventative Maintenance: Schedule and oversee routine maintenance for HVAC, plumbing, electrical, and specialized laboratory equipment (e.g., compounding hoods, mixers, and climate-control systems).
Clinical Application Specialist (MRI/CT/PACS Admin/Cardio/Ortho/Analytics) Sectra ABClinical Application Specialist (MRI/CT/PACS Admin/Cardio/Ortho/Analytics)NY$70,000–$90,000 / yearOur scalable and innovative enterprise imaging platforms allow healthcare organizations to expand across various specialties, while our secure communication systems provide unparalleled data protection. By joining Sectra, you'll be part of a team that delivers real value to society, providing solutions that improve patient care, increase healthcare efficiency, and enhance cybersecurity.
Medical Director Clinical Strategy Cohere Health Technologies LLCMedical Director Clinical StrategyNYRemote$250,000–$300,000 / yearBacked by leading investors such as Deerfield Management, Define Ventures, Flare Capital Partners, Longitude Capital, and Polaris Partners, Cohere Health drives more transparent, streamlined healthcare processes, helping patients receive faster, more appropriate care and higher-quality outcomes. Provide physician leadership in the creation of comprehensive research packages, investigating specific clinical areas/offerings and strategic partners of interest to strengthen the offering, then execute on cultivating any external partnerships and/or vendor relationships as necessary.
NewClinical Data Manager Integrated Resources, IncClinical Data ManagerWoodcliff Lake, New JerseyContractorPerform 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.
NewSenior Clinical Data Manager Integrated Resources, IncSenior Clinical Data ManagerWoodcliff Lake, New JerseyFull timeQualifications• Bachelor degree or above in scientific or related field Minimum 5-7 years' experience in Data Management with experience in managing projects, project teams• Experience with In-Form or other EDC software is desirable however, should have some experience in supporting Oncology studies• Must be able to work independently• Proficiency on all related regulations, GCP, and Good Clinical DM Practice• Project management skills required• Strong oral and written communication skills. Senior Clinical Data ManagerIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.