- Novo Nordisk Inc. (Plainsboro, NJ)
- …of clinical trials 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
- Novo Nordisk Inc. (Plainsboro, NJ)
- …of clinical trials improvement/innovation projects for NACD and Novo Nordisk (eg, clinical trial site staff, IRBs, clinical research vendors). ... risk identification and mitigation planning for assigned clinical trial sites Drives and tracks site activation and start-up activities with clinical … more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- … contracts, budgets, site payment and related reporting including global clinical trial financial transparency and Medicare, Medicaid, and SCHIP Extension ... practices.Lead GCO process improvement initiatives for the global reporting of GCO clinical trial spend. Financial Transparency (FT) and MMSEA Reporting… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …activities in collaboration with the CRO and the study team. Oversee the site qualification process.Monitor clinical trial performance and quality metrics ... disorders. Summary The incumbent will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions, in adherence to Good … 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
- 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
- Merck & Co. (North Wales, PA)
- …of 9 years Statistical Analysis System (SAS) programming experience in a clinical trial environment. MS (preferred) in Computer Science, Statistics, Applied ... of 7 years Statistical Analysis System (SAS) programming experience in a clinical trial environment. Required Experience and Skills: Experience leading large… more
- Merck & Co. (North Wales, PA)
- …or related field plus 9 years SAS programming experience in a clinical trial environment.MS in Computer Science, Statistics, Applied Mathematics, Life ... 7 or more years SAS programming experience in a clinical trial environment. Department Required Skills and...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… more
- Insmed Incorporated (Bridgewater, NJ)
- … Director of Biostatistics is responsible for the statistical aspects for complex clinical trial (s) or indication product line. This role leads the protocol ... section development, study setup, execution, analysis, and reporting of clinical trials, and interacts with cross-functional teams.ResponsibilitiesAdditional representative responsibilities… more
- Taiho Oncology (Princeton, NJ)
- …of timelines, budget, recruitment and country/ site selection strategies, and provision of clinical trial materials. + Serves as main study contact for the ... Associate Director, Clinical Operations Pleasanton, CA,...sites. + Responsible for the financial management of the clinical trial in conjunction with his/her supervisor… more
- Taiho Oncology (Princeton, NJ)
- Study Associate I, Clinical Operations Pleasanton, CA,...Knowledge, Skills, and Abilities: + 2 years of relevant clinical trial support or site ... Must possess the ability to multi-task and effectively prioritize in order to ensure clinical trial goals. + Recognize potential obstacles and work to resolve… 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
- J&J Family of Companies (Raritan, NJ)
- …will actively participate in or lead aspects of, medical review of clinical trial data, including adverse events, efficacy data, patient screening/eligibility ... Associate Director, Clinical Project Scientist -...Safety Management Plans * Performs medical monitoring/reporting, evaluates ongoing clinical trial data * Liaise with external… more
- Kelly Services (New York, NY)
- …aspects of a clinical trial including, but not limited to, clinical site selection, study visits, preparation of study contracts and budgets, and ... clinical study, including (but not limited to): + Clinical site selection + Site ...plan, case report forms, etc.). + Remain current on clinical trial regulatory requirements and guidelines (eg… more
- Actalent (Basking Ridge, NJ)
- …from monitoring plan + Monitors and updates investigator/ site status for the trial , and supports with clinical trial registry postings + Contributes ... Immediate Opening for Clinical Trials Assistant/ Associate Description: + ...+ Collates data for assessments such as feasibility and site selection and reviews site usability database… more
- Merck (Trenton, NJ)
- …+ Attend local Investigator Meetings if requested to. + Interface with GCTO partners on clinical trial execution. + Escalates site performance issues to CRM ... clinical trials. Under the oversight of the Clinical Research Director (CRD) or Head of Site...+ Expertise in and excellent working knowledge of core trial management systems and tools **Behavioral Competency Expectations:** +… 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
- Astrix Technology (New York, NY)
- …as needed for on- site monitoring visits. + Certification as a Certified Clinical Research Associate / Professional (CCRA / CCRP) or similar credential is ... Clinical Research Associate Clinical ...protocols. + Regionally based and involves working with multiple clinical trial sites across multiple protocols. +… more
- Merck (North Wales, PA)
- … Safety Statistics + Interact with Safety Physicians, Safety Scientists, Clinical Trial Physicians , Regulatory, Early/Late Development Statistics, Statistical ... skills. + Good understanding of worldwide regulatory requirements and clinical trial expertise . + Strong oral...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …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
