- Merck & Co. (Rahway, NJ)
- … Trial Assistant, Study Coordinator , Regulatory CTC ( Clinical Trial Coordinator ) or similar.MRLGCTO#EligibleforERPETJOBSNOTICE FOR INTERNAL ... and ensures continuity of site relationships through all phases of the trial .Performs clinical study site management/ monitoring activities in compliance… more
- Merck & Co. (Rahway, NJ)
- … Trial -Assistant, Study Coordinator , Regulatory CTC ( Clinical Trial Coordinator ) or similar.MRLGCTO#EligibleforERPETJOBSNOTICE FOR INTERNAL ... relationships and ensures continuity of site relationships through all-phases of the trial .Performs clinical study site management/ monitoring activities in… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …with the CRO and the study team. Oversee the site qualification process.Monitor clinical trial performance and quality metrics and share with study team, ... and immune disorders.SummaryThe incumbent will be responsible for ensuring execution of clinical studies across geographic regions, in adherence to Good Clinical … 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 ... rare diseases and immune disorders. Summary Assist in planning and execution of clinical studies, under the supervision of the Study Manager role the Study Associate… more
- Vitalief (Newark, NJ)
- …Join us and help clients adapt to evolving requirements in the research and clinical trial industry with cutting-edge solutions. Reasons to Work for Vitalief: + ... and managing patient care (patient retention). + Assist with monitoring patient visits. + Track deviations and documenting SAEs...of experience in Clinical Research as a Clinical Research Coordinator , with experience in patient… more
- New York University (New York, NY)
- …provide full-time intervention support on Systems Aligning for Equity (SAFE) Spaces, a clinical randomized control trial funded by The National Institute of ... Coordinator include: + Supporting management and organization of clinical and study data + Supporting student coach/trainee recruitment, on-boarding,… more
- Weill Cornell Medical College (New York, NY)
- …of trial activities and their rights as a study participant. + Performs monitoring of patients, collection and recording of clinical data. + Conducts patient ... Title: Assistant Research Coordinator Location: Upper East Side Org Unit: Parag...the coordination, implementation and management of all aspects of clinical research studies **Job Responsibilities** + Assists in the… more
- Merck (Rahway, NJ)
- …Clinical Trial Assistant, Study Coordinator , Regulatory CTC ( Clinical Trial Coordinator ) or similar. **MRLGCTO** **\#EligibleforERP** **ETJOBS** ... through all phases of the trial . + Performs clinical study site management/ monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws &… more
- Abbott (Manhattan, NY)
- …knowledge, procedure support (as needed), procedure outcomes and early indication of trends, clinical trial enrollment, and ICH-GCP and clinical research ... clinical sites + Promptly reports the findings of monitoring visits according to Abbott processes. + Maintain accurate,...needed, provide clinical and technical expertise for clinical trial procedure support + Attend study… more
- Weill Cornell Medical College (New York, NY)
- …**Experience** Approximately 5 or more years of related research experience in clinical trial management. **Knowledge, Skills and Abilities** + Knowledge of ... Title: Clinical Research Project Manager Location: Upper East Side...Completes all WCM regulatory submissions including Protocol Review and Monitoring Committee (PRMC), Institutional Review Board (IRB), Data Safety… 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 ... rare diseases and immune disorders. **Summary** Assist in planning and execution of clinical studies, under the supervision of the Study Manager role the Study… more
- HSS (New York, NY)
- …research budgets with sponsors for new studies and amendments. + Primary contact for clinical trial budget creation; oversees finances related to the clinical ... 2+ years of clinical research experience and comprehensive understanding of the clinical trial process + Proficiency in Microsoft Office suite + Excellent… more
- Hackensack Meridian Health (Hackensack, NJ)
- …audits, as well as ensuring ongoing compliance of study-related documentation throughout the clinical trial lifecycle for all assigned clinical trials. ... the Medicare Coverage Analysis, budget and contract for a clinical trial in order to initiate a...+ Certified Clinical Research Professional or Certified Clinical Research Coordinator or Society of … more
