- J&J Family of Companies (Trenton, NJ)
- …of day-to- day aspects of investigational site activities on assigned clinical trials. The Clinical Research Associate should ensure compliance ... Sr Clinical Research Associate - 2406209639W **Description**...for internal and external audits to ensure all essential clinical Trial Master File (TMF) documents are… more
- Bristol Myers Squibb (Princeton, 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
- System One (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 ... Role: Clinical Study Associate I Type: 12...information and coordinate with DS Regulatory Operations to post trial information on required public forums (eg.clinicaltrials.gov). Support Fair… more
- Bristol Myers Squibb (Princeton, NJ)
- …of smart systems and optimal approaches to support the end to end clinical trial data lifecycle, from collection through submission. + Holding accountability ... in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director, Clinical Data Standards is a...**Experience Requirements** + At least 12 years of global clinical trial expertise and a successful track… more
- Bristol Myers Squibb (Princeton, NJ)
- …clear product vision and strategy for the clinical data ecosystem especially with clinical trial design and data science methodologies to enable clinical ... team! **Position Summary:** We are seeking a highly motivated and detail-oriented Associate Director - Product Manager with broad clinical data experience… more
- WuXi AppTec (Plainsboro, 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
- Philips (Mercerville, NJ)
- …**Your role:** + Owning the overall study process and adherence to clinical trial procedures by keeping oversight, identifying possible problems/risks, creating ... ** Clinical Research Associate (Remote-Home Based)** Together...corrective actions using timely communication for daily monitoring and site mgmt. + Supporting site identification, selection,… more
- Bristol Myers Squibb (Princeton, NJ)
- …strong working knowledge of Pharmaceutical R&D business processes, particularly in Clinical Trial Operations, with demonstrated command of key concepts, ... enable Global Development Operations (GDO) function, specifically focusing on Veeva Clinical Vault (Veeva CTMS, Veeva eTMF). This role owns end-to-end responsibility… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …and the study team. Oversee the site qualification process. + Monitor clinical trial performance and quality metrics and share with study team, Operations ... will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions, in...work in collaboration with Outsourcing Procurement Management. + Lead trial feasibility and site identification activities in… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …from monitoring plan + Monitors and updates investigator/ site status for the trial , and supports with clinical trial registry postings + Performs ... to the clinical study team(s) responsible for clinical trial execution. The CSS may be...assignments from the Clinical Study Lead or Clinical Study Associate Manager. The CSS will… more
- Bristol Myers Squibb (Princeton, NJ)
- …more: careers.bms.com/working-with-us . Global Data Management (GDM) is responsible for clinical trial data acquisition, data standards governance, data ... trials across the BMS Research & Development portfolio. The Associate Director, External Data Acquisition is a leadership role...Acquisition is a leadership role with oversight of external clinical trial data acquisition and integration and… more
- Hackensack Meridian Health (Edison, 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
- Bristol Myers Squibb (Princeton, NJ)
- …Include : + Conduct risk assessments specific to medical affairs and clinical trial /research activities, utilizing a combination of data analytics, ... easy to understand policies specific to medical affairs and clinical trial /research activities that empower the business...out the highest potential of each of our colleagues. **On- site Protocol** BMS has a diverse occupancy structure that… more
- Bristol Myers Squibb (Princeton, NJ)
- …This includes a centralized triage function for informed consent negotiations with global clinical trial sites, IRBs/ECs, and health authorities, as well as ... internal and external best practices and exploring technologies. The Associate Director (AD), Informed Consent Management role reports to...Simplification. + Knowledge of IT systems used to support clinical trial processes and the authoring of… more
- Bristol Myers Squibb (Princeton, NJ)
- …leads the development and execution of statistical aspects for one or more clinical trials, including contribution to study trial design, analysis planning, ... their personal lives. Read more: careers.bms.com/working-with-us . **Purpose** The Associate Director, Biostatistics is a core member of cross-functional development… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …Research (CESR) projects. Candidates should have a comprehensive understanding of clinical trial management, with firsthand experience managing collaborative ... centered around rare diseases and immune disorders. **Summary:** The Associate Director will lead the execution and lifecycle management...to ensure timely follow-up and resolution of issues. + Clinical Trial Management: Oversee clinical … more
- Bristol Myers Squibb (Princeton, NJ)
- …the development and implementation of innovative strategies and technologies for clinical trial programming + Independently develops, validates, troubleshoots, ... towards industry experience + Proficient knowledge of drug development process, clinical trial methodology, regulatory guidance, industry standards, statistical… more
- Bristol Myers Squibb (Princeton, NJ)
- …towards industry experience + Proficient knowledge of drug development process, clinical trial methodology, regulatory guidance, industry standards, statistical ... work and in their personal lives. Read more: careers.bms.com/working-with-us . Associate Director, TA (Therapeutic Area) Analysis Standards Leader is accountable for… more
- Bristol Myers Squibb (Princeton, NJ)
- …in late stage drug development and activities required for and related to clinical trial initiation, maintenance and completion + Strong verbal and written ... to Senior Scientific Director Translational Medicine (TM), the TM Associate Director will be part of the late stage...group. The individual will be responsible for TM and clinical biomarker activities to support drug development programs in… more
- Bristol Myers Squibb (Princeton, NJ)
- …synopses and protocols. Contribute in cross-functional rapid response teams to respond to Clinical Trial Application (CTA) queries on new protocols and protocol ... clinical plans and marketing objectives. + Experience with clinical trial assays (CTA) in drug ...experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location.… more