- Mount Sinai Health System (New York, NY)
- …of experience in Phase I-IV clinical studies as a clinical trial assistant or clinical research associate is required. + Excellent Communication ... monitors all safety aspects of clinical research trial (s). Under guidance of the Associate Director...for adverse event reporting and tally. This includes evaluating clinical database for non- site reported adverse events… 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
- 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 (Berkeley Heights, 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
- Gilead Sciences, Inc. (Parsippany, NJ)
- …Join Gilead and help create possible, together. **Job Description** The Clinical Trial Capabilities (CTC) organization offers infrastructure, support, and ... Operations and Development Organizations with rapid, efficient, and compliant clinical trial execution to deliver transformative medicines to patients.… more
- IQVIA (Parsippany, NJ)
- …may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF)… 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 (Linden, NJ)
- …may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF)… 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)
- **Job Description** The Associate Vice President (AVP)/Section Head, Global Clinical Development, Ophthalmology will focus on driving strategy, development, and ... for clinical programs. + Supervises development of clinical documents including development plans, protocols, trial ...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… more
- Philips (Stamford, CT)
- …**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
- IQVIA (Parsippany, NJ)
- **Role Overview:** As a Clinical Research Associate , you'll be at the forefront of ensuring our study sites operate smoothly and efficiently. Your work will be ... to ensure smooth study progress. + **Documentation:** Maintain essential documents in the Trial Master File (TMF) and Investigator's Site File (ISF) as per… more
- Hackensack Meridian Health (Hackensack, NJ)
- …+ Maintains accurate, complete, up-to-date records on each patient participating in a clinical trial protocol in all applicable systems (ie electronic medical ... record, clinical trial management system, departmental and protocol...Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified … 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 (New York, NY)
- IQVIA is seeking a Senior Clinical Research Associate with at least 2 years of monitoring experience in one of the following therapeutic areas: Central Nervous ... copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF)… more
- IQVIA (Parsippany, NJ)
- **Job Overview** Join our team as a Clinical Research Site Manager, where you'll play a crucial role in ensuring our study sites operate seamlessly and adhere to ... initiation, monitoring, and close-out visits in line with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH)...the start-up phase as required. + **Documentation:** Ensure all site documents are filed in the Trial … 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
- Hackensack Meridian Health (Hackensack, NJ)
- …15. Maintains accurate, complete, up-to-date records on each patient participating in a clinical trial protocol in all applicable systems (ie electronic medical ... record, clinical trial management system, departmental and protocol...Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified … more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …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
- 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