- Novo Nordisk (Plainsboro, NJ)
- …of clinical trials improvement/innovation projects for NACD and Novo Nordisk (eg, clinical trial site staff, IRBs, clinical research vendors). ... identification and mitigation planning for assigned clinical trial sites + Drives and tracks site ...tracks site activation and start-up activities with clinical trial sites to support trial… more
- ThermoFisher Scientific (New York, NY)
- … clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy ... Impactful Work:** Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts...study systems are updated per agreed study conventions (eg Clinical Trial Management System, CTMS). Performs QC… more
- Abbott (Manhattan, NY)
- …of trends, clinical trial enrollment, and ICH-GCP and clinical research application Adheres to specified site nomination, qualification, and startup ... clinical staff (eg, operations management, study team, Site Contracts Associate ), as needed. **Manage all...needed, provide clinical and technical expertise for clinical trial procedure support + Attend study… more
- WuXi AppTec (Cranbury, NJ)
- **Overview** The Clinical Research Associate III Senior Oncology performs and coordinates aspects of field-based and office-based monitoring and data quality ... clinical monitoring and required reporting, including pre-study visits, site invitation visits, routine monitoring visits (both onsite and...or supervisor, including but not limited to mentoring of Clinical Research Associate (CRA) I and II… more
- Merck (Rahway, NJ)
- …members including clinical directors and study managers to lead/support clinical trial scientific activities. **Job Responsibilities** + Responsible for the ... clinical protocol(s). + Serves as the lead clinical scientist on the clinical trial...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… more
- IQVIA (Queens County, NY)
- …SOPs, policies and practices. **_Immediate need for candidates with CNS Clinical Trial Management experience._** **RESPONSIBILITIES** + Accountable for ensuring ... the integrated study management plan/project management plan. + Accountable for the clinical delivery (subject recruitment, site management, data integrity) per… more
- Hackensack Meridian Health (Neptune, NJ)
- …works under the general supervision of the principal investigator responsible for the clinical trial (s) to which is assigned. **Responsibilities** + Acts as ... on each protocol and each patient participating in a clinical trial protocol in the clinical...SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified … more
- Novo Nordisk (Plainsboro, NJ)
- … deliverables across NACD. This includes leading processes and technology improvements to link Clinical trial site needs, Finance and Supply forecasts that ... US and CA warehouses operations for US and CA Clinical Trial sites. Accountable for overall performance...projects for NACD & Novo Nordisk (eg Investigators and site staff, vendors etc.). Establish and manage senior level… more
- Merck (Rahway, NJ)
- …stakeholders including the Global Project Manager, Alliance Manager, Global Trial Manager, Clinical Sub Team, Clinical Trial Team, Outsourced Trial ... and improve lives. **Position Description:** Under the guidance of the Oncology Clinical Development Finance Associate Director, the Finance Senior Specialist… more
- Bristol Myers Squibb (Berkeley Heights, NJ)
- …the development and implementation of innovative strategies and technologies for clinical trial programming. A ssociate Director develop collaborative ... the development and implementation of innovative strategies and technologies for clinical trial programming + Independently develops, validates, troubleshoots,… more
- Memorial Sloan-Kettering Cancer Center (New York, NY)
- …employees. Job Description Exciting opportunity at MSK: Join our team as aRegulatory Associate , Prostate Cancer Clinical Trial Consortium! We're looking for ... regulatory documentation is complete, up-to-date, and accurate, and that site qualifications are maintained throughout the duration of a...compliance of such trainings for all involved in the clinical trial . Key Qualifications: + 2-7 years… more
- Merck (Rahway, NJ)
- …minimum of 9 years Statistical Analysis System (SAS) programming experience in a clinical trial environment. + MS (preferred) in Computer Science, Statistics, ... of 7 years Statistical Analysis System (SAS) programming experience in a clinical trial environment. **Required Experience and Skills:** + Experience leading… more
- Hackensack Meridian Health (Neptune, NJ)
- …contain accurate, complete and up-to-date records of each patient participating in a clinical trial and reviews source documents for completeness. + Provides ... : + SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research… more
- Merck (Rahway, NJ)
- …translational PK/PD approaches, population pharmacokinetic models, exposure-response models, clinical trial simulation, disease progression models, quantitative ... and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial applications… more
- Pfizer (New York, NY)
- …communication of statistical analyses, data presentations, and scientific reports, including clinical trial results, exploratory and meta-analysis results **,** ... + A minimum of 4 years' experience in the clinical trial setting (preferably in oncology of...dental and vision coverage. Learn more at Pfizer Candidate Site - US Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures… more
- Merck (Rahway, NJ)
- …(popPK), PK/PD models, exposure response (ER) models, model-based meta-analysis (MBMA), clinical trial simulations (CTS) and disease progression modeling into ... our company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas....seek to improve cycle time, cost/size, number of trials, clinical trial design and Go/No Go decisions… more
- Merck (Rahway, NJ)
- … pharmacology, biomarkers of target engagement, experimental medicine platforms, early clinical trial designs and conduct, and operational understanding for ... **Job Description** The Associate Vice President (AVP)/Therapeutic Area Head, Immunology Translational...strategy, bridging the continuum from Discovery Research through Late-Stage Clinical Development. The AVP provides strategic oversight for the… more
- Danaher Corporation (New York, NY)
- …related professional role. + Fundamental knowledge and good understanding of GCPs, clinical trial design, study development and project management. + Experience ... our office in remotely based in the USA Study site and study coordinator Come join a fantastic team!...clinical /medical science. + 5+ years' experience as a Clinical Research Associate , Clinical Project… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …team of outsourcing managers within a specific therapeutic area(s) and manages clinical trial vendor partnerships that supports alliance and outsourcing ... management across multiple service categories of clinical trial activities in R&D. **Key Responsibilities**...R&D. **Key Responsibilities** + Leads a team of Outsourcing Associate Directors and Managers within a specific TA, and… more
- New York State Civil Service (Brooklyn, NY)
- …and preparing detailed written reports of investigative findings. Substitution:an associate degree in criminal justice, cyber security, law enforcement, police ... child protective services investigator, in an investigative position involving trial preparations and detailed reports, or investigations within a branch… more