Research Biostatistician I Weill Cornell Medical CollegeResearch Biostatistician INew York, NY$90,000–$104,200 / yearCornell 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." Analyzes health care data and health care claims data using basic and advanced statistical methodologies, interprets results for investigators, and prepares reports.
Project Associate Research Foundation of The City University of New YorkProject AssociateNew York, New YorkThe Behavioral Health Care Coordination training program has been operating from the Hunter College, CUNY, School of Social Work (Silberman) in collaboration with the New York State Office of Mental Health and the New York City Department of Health and Mental Hygiene since July, 1990. The goal of the BHCC training program is to provide Care Coordinators and Care Coordination Supervisors with essential skills to ensure whenever possible that consumers are maintained in the least restrictive community environment.
NewAssistant Director of HR: Payroll Research Foundation of The City University of New YorkAssistant Director of HR: PayrollNew York, New York$117,442–$137,015 / yearThe Assistant Director ensures adherence to federal, state, and local payroll regulations, maintains payroll integrity within Workday (aka OneRF) and related systems with a strong emphasis on post-implementation stabilization, optimization and continuous improvement. Working in close partnership with the Payroll Manager, the Assistant Director supervises a team of Campus Payroll Coordinators in administering all aspects of payroll management and serves as a subject matter expert.
Senior Counsel, Anti-Counterfeiting Chanel S.A.Senior Counsel, Anti-CounterfeitingNew York, NYCareer and Leadership Development: We have dedicated in-house teams focused on supporting the onboarding of employees, developing leadership skills via custom programs like Imagine Chanel People, Heart of Leadership and group and individual coaching, and blended online and live classes offered on our Bloom platform and by skilled trainers, such as Shape Your Career, to develop career building skills. In partnership with the U.S. Head of Intellectual Property, you will safeguard the integrity of the House-protecting brand equity, craftsmanship, and client trust by leading the U.S. anti-counterfeiting program across online/digital and brick-and-mortar environments.
Associate Director, Compliance & Ethics Investigations Bristol-Myers Squibb CoAssociate Director, Compliance & Ethics InvestigationsPrinceton, NJ$157,080–$190,344 / yearProven successful investigation/project management in developing and executing all phases of an investigation plan including: collection, review and analysis of data, information and records; conducting interviews; documenting work completed; drafting findings and conclusions; accountability for successful completion. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
NewInternal Medicine Field Medical Antiviral FMD, Senior Director, non-MD PfizerInternal Medicine Field Medical Antiviral FMD, Senior Director, non-MDNew York City, New YorkIn addition to the AV FMD territory responsibilities listed below, this Senior Director–level AV FMD role responsibilities also include but are not limited to: Representing the FMD role on the assigned LCM clinical study team(s) and proposing appropriate FMD early engagement activities for endorsement by the AV FMD TLs and IM FMD Group VP; Conducting the appropriate training for FMDs (in collaboration with the respective study teams) on how to compliantly engage with clinical trialists and ensure the FMDs have the requisite protocol knowledge and understanding of the respective LCM protocols; Recommending and ensuring approval of relevant medical content and related materials FMDs will need with which to engage these contracted clinical trialists; Mentoring additional FMD colleagues that may be identified to assist in representing the FMD group on the clinical study team(s); Developing processes to track, measure, and characterize the impact of the FMD earlier engagement work for the assigned LCM clinical program working with key cross-functional partners in R & D, Global Medical Affairs, and MEI; Ensuring FMD leadership is aligned with and endorses the respective LCM early engagement support and maintain effective relationships with the respective internal cross-functional partners. In collaboration with US and/or Global Medical Affairs colleagues, partner with IM/SC Research & Development and Global Product Development (GPD) in the identification of potential sites for Pfizer-sponsored clinical trials, including identification of sites serving under-represented patient populations in trials.
NewInternal Medicine Field Medical Antiviral FMD, Senior Director, MD PfizerInternal Medicine Field Medical Antiviral FMD, Senior Director, MDNew York City, New YorkIn addition to the AV FMD territory responsibilities listed below, this Senior Director–level AV FMD role responsibilities also include but are not limited to: Representing the FMD role on the assigned LCM clinical study team(s) and proposing appropriate FMD early engagement activities for endorsement by the AV FMD TLs and IM FMD Group VP; Conducting the appropriate training for FMDs (in collaboration with the respective study teams) on how to compliantly engage with clinical trialists and ensure the FMDs have the requisite protocol knowledge and understanding of the respective LCM protocols; Recommending and ensuring approval of relevant medical content and related materials FMDs will need with which to engage these contracted clinical trialists; Mentoring additional FMD colleagues that may be identified to assist in representing the FMD group on the clinical study team(s); Developing processes to track, measure, and characterize the impact of the FMD earlier engagement work for the assigned LCM clinical program working with key cross-functional partners in R & D, Global Medical Affairs, and MEI; Ensuring FMD leadership is aligned with and endorses the respective LCM early engagement support and maintain effective relationships with the respective internal cross-functional partners. In collaboration with US and/or Global Medical Affairs colleagues, partner with IM/SC Research & Development and Global Product Development (GPD) in the identification of potential sites for Pfizer-sponsored clinical trials, including identification of sites serving under-represented patient populations in trials.
Manager, Global Production Management Sumitomo Mitsui Banking CorpManager, Global Production ManagementJersey City, NJ$165,000–$170,000 / yearSupervise and guide a team of engineers who perform the day to day work, have responsibility for the system operation management, make systems available at the correct time, respond to alerts that are generated by systems and ensure that the work to address the alerts are allocated to the correct support team and resolved, and monitor the systems environment to prevent system issues. (SMBC), SMBC Nikko Securities America, Inc., SMBC Capital Markets, Inc., SMBC MANUBANK, JRI America, Inc., SMBC Leasing and Finance, Inc., Banco Sumitomo Mitsui Brasileiro S.A., and Sumitomo Mitsui Finance and Leasing Co., Ltd.
Director Biostatistics in Princeton, New Jersey, United States of America | Development Operations at Genmab Government of DenmarkDirector Biostatistics in Princeton, New Jersey, United States of America | Development Operations at GenmabPrinceton, NJDirector Biostatistics in Princeton, New Jersey, United States of America | Development Operations at Genmab Skip to main content Skip to main content Healthcare Professionals Patients & Care Partners Partnerships Contact Working at Genmab Career Areas Application Process Locations Talent Community Job Search Corporate Sign in Close the popup Sign in to Phenom Careers Enjoy a personalized jobs search Sign in with Google Employee Login Sign in with Google Sign up Saved jobs (0) Healthcare Professionals Patients & Care Partners Partnerships Contact Saved jobs (0) Toggle navigation - - Recruitment Fraud Warning: Please note that Genmab never requests payment, banking details, or Social Security numbers during the recruitment process. Close Covid-19 banner Director Biostatistics Category Development Operations Job Id R17259 Remote This job available in 3 locations Princeton, New Jersey, United States of America Copenhagen, Capital, Denmark Utrecht, Netherlands Save Apply Now We are extra[not]ordinary*(ex· tra· not· or· di· nary |\ ik- str-not- r-d - ner- ) Adjective: A unique word for Genmab meaning to go way beyond what is usual; to be remarkable; proudly unique and authentic Back to search results Previous job Next job JOB DESCRIPTION At Genmab, we are dedicated to building extra[not]ordinary futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases.
Grants Manager Columbia UniversityGrants ManagerNew York, NY$75,000–$85,000 / yearReporting to the Associate Director of Finance and Administration (DFA), the Grants Manager is the lead administrator for pre- and post-award grant activities, acting as the department's representative to sponsoring agencies. At least 3 years of relevant experience in a research administration environment, Collaborate with the Associate Director of Finance & Administration to implement operational priorities and track performance metrics.
Director/Senior Director, Clinical Development SystImmune, Inc.Director/Senior Director, Clinical DevelopmentPrinceton, NJ$230,000–$300,000 / yearSystImmune is seeking an experienced Director/Senior Director of Clinical Development to lead the direction, planning, execution, and interpretation of clinical trials within the Clinical Development program. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs).
Program Coordinator, TMP Columbia UniversityProgram Coordinator, TMPNew York, NY$66,300–$67,000 / yearThe TechMPower (TMP) project is looking for a Program Coordinator to support a 4-year, NIDA-funded innovative study that aims to prevent and treat HIV and overdose in criminal justice settings through the implementation of a comprehensive bundle of evidence-based strategies that will enhance the effective delivery of interventions for both HIV and substance use disorder (SUD). Support TMP events as directed by the Project Director, including organizing planning meetings and events related to the Community Advisory Board and TMP implementation strategies (Trainings, coalition workgroup meetings, implementation team meetings, and navigation case management) as needed.
New["Document Management Analyst II","Document Management Analyst II"] Contact Government Services Llc["Document Management Analyst II","Document Management Analyst II"]New York$48,000–$52,000 / yearDrafting investigatory subpoenas and discovery requests; -Reviewing and analyzing documents and information obtained during investigations or turned over during litigation discovery, preparing demonstrative exhibits and aiding attorneys in presentations, meetings and court proceedings; -Researching, collecting and analyzing data, developing metrics, statistics and other tracking methods to measure and assess the data; creating and maintaining databases and constructing complex database queries; converting complex data into easily comprehensible reports, PowerPoint presentations and other data visualizations for investigations and litigation; -Assisting in the preparation for and participating in witness interviews and depositions; -Analyzing incoming information to identify violations of the Controlled Substances Act and/or the False Claims Act; -Reviewing electronic evidence using platforms such as Relativity; -Data mining and organization; -Data analysis using Excel, Access and similar software; -Coordination with investigators, consultants and expert witnesses; -Preparing talking points, presentations and other materials; -Working collaboratively with Assistant U.S. Attorneys and legal support staff. CGS is searching for a Document Management Analyst to help support the Civil Division of a large federal agency in addressing civil pandemic- related healthcare fraud and/or opioid-related matters.
Assistant /Associate Professor Movement Disorder RWJBarnabas HealthAssistant /Associate Professor Movement DisorderNew Brunswick, NJParticipate in community service responsibilities of the department in such areas as providing neurological care for indigent patients and teaching or advising lay community groups in multiple areas relating to movement disorders, including deep brain stimulation, in coordination with the Department of Neurosurgery. Qualifications: MD Candidates must be graduates of an ACGME-accredited neurology residency, be board certified or eligible in neurology; have completed a fellowship in movement disorder or related clinical neurosciences and be eligible for a New Jersey License.
Research Associate Case Western Reserve UniversityResearch AssociateNew York, NY$56,000–$61,000 / yearA strong background in qualitative and quantitative methodologies, the design and conduct of clinical research/clinical trails, building and managing data mangement systems including routine quality control of data and report generations is highly desirable. CWRU considers factors such as (but not limited to) the specific grant funding and the terms of the research grant, as well as the scope and responsibilities of the position, candidate's work experience, education/training, key skills, and internal peer equity.
Senior Medical Director, Hematology Pfizer IncSenior Medical Director, HematologyNew York City, NY$274,500–$444,100 / yearIn this role, you will: • Clinical Development Leadership on Study Teams and Development Subteams • Serves as the Clinical Development Lead on subteams including for Marketing Authorization Applications • Conduct medical monitoring activities including eligibility assessment, data review and safety monitoring • Lead peer-to-peer interactions with investigator • Serve as the point of contact for clinical issues between the study team, investigators • Lead and contribute to development and maintenance of clinical trial and regulatory documents, in collaboration with Clinical Scientist and the cross-functional team. • Medical degree with 5+ years clinical/industry experience • Hematology/Oncology clinical experience in academia/industry • Late-stage clinical development experience • Experience overseeing and providing clinical development leadership across several study teams • Excellent communication skills to present complex technical concepts to colleagues from all disciplines and levels • Strong strategic and analytical skills.
Clinical Research Nurse VitaliefClinical Research NurseNew Brunswick, NJDeliver high-quality, compassionate, hands-on oncology nursing care while coordinating closely with investigators, clinical teams, and ancillary departments (e.g., pathology, radiology, clinical laboratory, surgery, infusion services) in accordance with study protocols, treatment plans, and Good Clinical Practice (GCP) guidelines. IMPORTANT NOTE: Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis.
Clinical Study Specialist ICON PlcClinical Study SpecialistBasking Ridge, NJCompiles study manuals including but not limited to: study reference binders and manuals and maintains versioning of study reference materials (e.g., regulatory, pharmacy, and laboratory binders. Tracks and monitors close out activities - study close-out documents (1572s, Investigational Product reconciliation, Financial Disclosures, etc.) and CRA close-out visits.
Research Scientist Network Systems Peraton IncResearch Scientist Network SystemsBasking Ridge, NJ$135,000–$216,000 / yearPeraton Labs'' cybersecurity and network research protects mission-critical systems and national cyber infrastructure and efficiently utilizes spectrum and system resources by employing technologies in the areas of computer network defense, secure-by-design, AI/ML and deterministic and stochastic optimization. Required Qualifications: Minimum of 8 years of experience with BS/BA; Minimum of 6 years with MS/MA; Minimum of 3 years with a PhD in Computer Science, Computer Engineering, Electrical Engineering, Applied Mathematics, Physics, or related scientific/engineering disciplines.
Door Guard - Uniformed Saks OFF 5THDoor Guard - UniformedElizabeth, NJYour Life and Career at Saks OFF 5TH: Be part of an empowered, innovative team; work with an adventurous spirit and a customer-centric mindset; play a critical role in making decisions that will position us to win. Your Life and Career at Saks OFF 5TH: Be part of an empowered, innovative team; work with an adventurous spirit and a customer-centric mindset; play a critical role in making decisions that will position us to win.