- Edwards Lifesciences (Trenton, NJ)
- …subject documentation is within parameters of study hypothesis, as well as monitoring clinical trial/study safety, in keeping with protocols, GCP (Good ... skills. + Providing input on strategic direction on field monitoring of studies and data collection for clinical...cardiology trials + Master's Degree in related field + Clinical research certification (ACRP or SoCRA … more
- Parexel (Trenton, NJ)
- …Specialist, Clinical Data Scientist) + May act as a Mentor for Clinical Research Associates **Skills:** + Monitoring Experience: Minimum 3 years ... (DSMM) + Partners with SCP and Country Study Operations Manager (SOM) + When required Partners with other Study...relevant experience in clinical research site monitoring (preferably 2 years in… more
- Parexel (Trenton, NJ)
- …Remote - Need for SE Region - FL** **ONCOLOGY preferred** **Job Purpose:** The Clinical Research Associate (CRA) has local responsibility for the delivery of the ... delivery of the study. The CRA is responsible for the preparation, initiation, monitoring , and closure of assigned sites in clinical studies, in compliance… more
- Parexel (Trenton, NJ)
- The Senior Clinical Research Associate (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the ... delivery of the study. The SrCRA is responsible for the preparation, initiation, monitoring , and closure of assigned sites in clinical studies, in compliance… more
- Parexel (Trenton, NJ)
- MUST HAVE AT LEAST ONE YEAR OF DIRECT CENTRAL MONITORING EXPERIENCE The Manager , Central Monitoring is accountable for centralized monitoring activities ... data and presenting as an integral member of the Clinical Study team for clinical development studies....interpreted, reported and presented to the study teams. The Manager , Central Monitoring , will be responsible for… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Senior Clinical Research Director **Location:** Cambridge, MA or Morristown, NJ **About the Job** Join the engine of Sanofi's mission - where deep ... the impossible into possible for millions. As the **Senior Clinical Research Director** (Senior CRD) within the...review of data within the scope of the Centralized monitoring , clinical and medical information for the… more
- Vitalief (New Brunswick, NJ)
- …in New Brunswick, NJ. Job Responsibilities: + Under the direct supervision of the Nurse Manager of Clinical Research Center (CRC), you will be responsible ... and managing patient care (patient retention). + Assist with monitoring patient visits. + Track deviations and documenting SAEs...Minimum of 1 to 2 years of experience in Clinical Research as a Clinical … more
- Regeneron Pharmaceuticals (Warren, NJ)
- …landscape + Applies basic scientific expertise to support initiation and execution of clinical research and development studies for early and/or late stage ... The Senior Manager , Hematology, Clinical Scientist leads in...seeking proven knowledge of the drug development process, Good Clinical Practice, study design, clinical research… more
- Taiho Oncology (Princeton, NJ)
- …Under minimal supervision, leads and manages complex global studies to support the Clinical Development Plan. The Senior Study Manager (SSM) is responsible for ... and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources… more
- Vitalief (New Brunswick, NJ)
- …partner working at the intersection of Sites, Sponsors, and CROs across the research and clinical trials landscape. By blending deep subject matter expertise ... that ultimately benefit patients. We are seeking a problem-solving, "hands-on" Grants Manager to join our exceptional client team. WHY VITALIEF? + You can… more
- Regeneron Pharmaceuticals (Warren, NJ)
- …ICH/GCP. This role applies to internally sourced studies and studies out-sourced to Clinical Research Organizations (CROs) and the balance of direct leadership ... point of contact for IVRS issues, and support oversight of unmasked clinical monitoring + Responsible for direct supervision of CTM staff. Line management… more
- IQVIA (Parsippany, NJ)
- …- Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements ie ICH GCP and relevant local laws, ... understanding of project financials. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …sciences or related field; advanced degree a plus. + 6-8 years of experience in clinical quality assurance or clinical research within the pharmaceutical or ... **Job Summary** The Senior Manager of Global Quality Management (GQM) supports the...of Global Quality Management (GQM) supports the execution of clinical quality activities to ensure compliance with Good … more
- Bristol Myers Squibb (Princeton, NJ)
- …* Global experiences since this position has responsibility for strategy and clinical research in oncology in multiple geographies. **Key Competency ... the context of autoimmune disease * Supervises the development, monitoring , analysis, and interpretation of clinical trials...their inputs on emerging science in drug and biomarker research , disease knowledge, and design of clinical … more
- Medtronic (Morristown, NJ)
- …you will be driving sales growth and market share by promoting our Respiratory & Monitoring Solutions portfolio to key clinical leaders in the ICU, General Care ... valid driver's license is essential for this role. Medtronic's Acute Care & Monitoring (ACM) business works together with the global healthcare community to solve… more
- Sanofi Group (Morristown, NJ)
- …+ External contacts: Investigators, Clinical Site Services Providers, early phase Clinical Research Organizations, clinical trial vendors, clinical ... + External contacts: Investigators, Clinical Site Services Providers, early phase Clinical Research Organizations, clinical trial vendors, clinical … more
- Bristol Myers Squibb (Princeton, NJ)
- …manage a group of professionals including MDs or PhDs or PharmDs with clinical research experience. + The successful candidate will understand early-stage drug ... development plans + This leader will supervise the development, monitoring , analysis and interpretation of clinical trials...plus since this position has responsibility for strategy and clinical research in oncology in multiple geographies… more
- Regeneron Pharmaceuticals (Warren, NJ)
- …other departments + Applies advanced scientific expertise to propose, design, and execute clinical research and development studies for early and late stage ... of the Clinical Study Team and Global Clinical SubTeam + Line Manager for CS...and/or reviews documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical … more
- Bristol Myers Squibb (Princeton, NJ)
- …other scientific field preferred) **Experience Requirements** + 5+ years of experience in clinical science, clinical research , or equivalent + Proficient ... and in their personal lives. Read more: careers.bms.com/working-with-us . The Senior Clinical Scientist reports through the Clinical Science function which… more
- Bristol Myers Squibb (Princeton, NJ)
- …in order to gain their inputs on emerging science in drug and biomarker research , disease knowledge, and design of clinical development studies and programs * ... at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Clinical Trial Physician sits within Clinical Development, which is a… more