- Novo Nordisk (Stamford, CT)
- …of clinical trials and improvement/innovation projects for NACD and Novo Nordisk (eg, clinical trial site staff, clinical research vendors). Manages ... Development (NACD) goals, including successful delivery of studies within the clinical trial portfolio. Contributes to local or increasingly complex… 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
- Bristol Myers Squibb (Madison, NJ)
- …Summary / Objective** + Responsible for implementation, planning, and execution of assigned clinical trial activities. Serves as Clinical Trial ... team members + May support clinical development planning (collaboration with Clinical Development Lead/ Clinical Trial Physician for provision and… more
- Merck (Rahway, NJ)
- …and SAP team members to further extend capabilities and functionalities on our existing Clinical Trial Supply Management (CTSM) solution in order to satisfy and ... Management and Distribution areas with a strong focus in Clinical Trial Supply Management (CTSM) is highly...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… more
- J&J Family of Companies (Raritan, NJ)
- …in optimizing our site engagement strategies and facilitating successful clinical trial operations globally. **Key Responsibilities:** + Collaborate closely ... Associate Director, Site Engagement Strategy -...impact to participant health and wellbeing by reinventing the clinical trial experience. The Innovative Health Engagement… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and ... clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good … more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …the TMF technical capabilities and oversight of standardization, training, quality, and timely clinical trial documentation across the clinical program. The ... impact. Join Gilead and help create possible, together. **Job Description** The Associate Director, Clinical Records & Information Management will partner with… 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
- IQVIA (Parsippany, NJ)
- …may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... in accordance with contracted scope of work and Good Clinical Practice. * Work with sites to adapt, drive,...site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's… more
- Merck (Rahway, NJ)
- …+ Attend local Investigator Meetings if requested to. + Interface with GCTO partners on clinical trial execution. + Escalates site performance issues to CRM ... will be key to ensure strong monitoring in our clinical trials. Under the oversight of the CRD or...Under the oversight of the CRD or Head of Site Management and Monitoring, the person is responsible to… more
- Merck (Rahway, NJ)
- …Point of Contact (POC) for assigned protocols and link between Country Operations and clinical trial team (CTT). + Responsible for project management of the ... and escalates performance issues and training needs to CRA ( Clinical Research Associate ) manager and/or functional vendor...country roles ensuring a strong collaboration (including the CTC Clinical Trial Coordinator, CRAs and COM … more
- Hackensack Meridian Health (Hackensack, NJ)
- …change. The Clinical Research Nurse is responsible for coordinating and overseeing clinical operations of a clinical trial and participates in assessing, ... complete, up-to-date records on each patient participating in a clinical trial protocol in all applicable systems...Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified … 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 (Hackensack, NJ)
- …change. The Clinical Research Nurse is responsible for coordinating and overseeing clinical operations of a clinical trial and participates in assessing, ... complete, up-to-date records on each patient participating in a clinical trial protocol in all applicable systems...Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified … more
- Regeneron Pharmaceuticals (Armonk, NY)
- …the Clinical Study Lead (CSL) by taking responsibility for areas of clinical trial delivery. This role applies to internally sourced studies and studies ... based in Armonk, NY or Basking Ridge, NJ._ A Clinical Study Associate Manager (CSAM) role supports...maintenance of study systems including but not limited to Clinical Trial Management System (CTMS) and … more
- Hackensack Meridian Health (Nutley, NJ)
- …works under the general supervision of the principal investigator responsible for the clinical trial (s) to which is assigned. **Responsibilities** A day in the ... 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
- AbbVie (Florham Park, NJ)
- …knowledge of database concepts. + Experienced in the life sciences domain and clinical trial processes + Demonstrated ability to influence others without direct ... bringing people, process, and technology together to generate business value from clinical trials data. Our operational model is exemplified through execution and… more
- Merck (Rahway, NJ)
- …and sustained. The Sr CCQM Lead supports large to medium size country/cluster clinical trial operations to achieve those objectives. Under the guidance of ... and/or functional lines. This includes line management of Country Clinical Quality Managers (CCQMs) and Associate Country...line management position. + Deep knowledge and understanding of Clinical Trial processes, GCP and applicable … more
- Bristol Myers Squibb (Madison, NJ)
- …projects * Efficiently plans, coordinates, and delivers complete, high quality and reliable clinical trial data in a timely manner for assigned projects * ... R&D pipeline . This role may report into Director, Clinical Data Management or Associate Director, ...functional study team members to ensure on-going review of trial data currency , quality and completeness * Represents… more
- Pfizer (Pearl River, NY)
- …Designs clinical studies to meet the stated objectives of a program. Assures that clinical trial objectives of each study fit with the clinical program ... to enable quality, compliance and patient safety at the trial , site and patient level. + Accountable...+ Provides protocol specific training to study team, investigators, clinical research associate , and others. + Interacts… more