- IQVIA (Parsippany, NJ)
- …in lieu of degree. * In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, ie, Good Clinical Practice (GCP) and ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
- IQVIA (Parsippany, NJ)
- …in lieu of degree. * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. * ie, Good Clinical Practice (GCP) ... IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in… 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 ... all protocols, regulations, and sponsor requirements. **Essential Functions** + **Site Monitoring:** Conduct selection,...and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
- IQVIA (New York, NY)
- …according to local requirement. **MINIMUM RECRUITMENT STANDARDS:** + **2.5 years of clinical research coordination experience at site level** + Nursing or ... of education, training and experience IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
- IQVIA (Parsippany, NJ)
- **Position Summary** The Clinical Research Associate (CRA) will be responsible for designing, planning, coordinating, and conducting all activities involved ... Skills and Knowledge Requirements** + ≥2 years of experience as a Clinical Research Associate , with specific in vitro diagnostics study experience +… more
- IQVIA (Parsippany, NJ)
- …and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have: + A Bachelor's degree ... or at least three months of on-site monitoring experience. 2 years of clinical research coordinator experience strongly preferred. + Alternatively, you should… more
- Caris Life Sciences (New York, NY)
- …Communicate effectively with the research team, investigator(s), Clinical Research Associate (s), study sponsor and ancillary staff. **Required ... case report forms and other information related to data collection for clinical research . Must respond to queries in a timely fashion. Schedule on-site visits… more
- Mount Sinai Health System (New York, NY)
- **Job Description** The Clinical Research Associate is an integral part of the research study team and monitors all safety aspects of clinical ... studies as a clinical trial assistant or clinical research associate is required....all study related correspondence with the investigative sites and sponsor including, but not limited to associated correspondence, CEC… more
- Hackensack Meridian Health (Hackensack, NJ)
- …Preferred** : + Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical ... and serve as a leader of positive change. The ** Clinical Research Nurse** is responsible for coordinating...research finance personnel. + Prepares and assists for sponsor monitor site visits and ensures all supporting documentation… more
- Hackensack Meridian Health (Hackensack, NJ)
- …Preferred:** + Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical ... healthcare and serve as a leader ofpositive change. The Clinical Research Nurse is responsible for coordinating...research finance personnel + Prepares and assists for sponsor monitor site visits and ensures all supporting documentation… more
- Hackensack Meridian Health (Edison, NJ)
- …: + SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical ... to transform healthcare and serve as a leader of positive change. The ** Clinical Research Coordinator** is responsible for coordinating and overseeing … more
- Mount Sinai Health System (New York, NY)
- **Job Description** The Clinical Research Nurse is a Registered Professional Nurse who is responsible for assisting in the assessment, management, and ... coordination of care for subjects enrolled onto IRB approved research studies/ clinical trials, as specified by the research protocol, across the continuum of… more
- Intra-Cellular Therapies, Inc (Bedminster, NJ)
- …of approved and investigational compounds across different stages of clinical development. Our lead candidate, lumateperone (CAPLYTA(R)), is FDA-approved for ... bipolar depression in adults as monotherapy and as adjunctive therapy. ** Associate Director/Director, Data Management** will oversee and provide guidance (both… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. **Summary** This is ... and approvals and associated interactions with vendors. Supports regular vendor/ sponsor discussions to identify risks and ongoing study support. Identifies… more
- Research Foundation CUNY (New York, NY)
- …Programs (GSP) Office of the CUNY School of Medicine and Reporting to the Associate Dean for Research , the GSP Director manages and supports full-time staff ... and works closely with the Associate Dean for Clinical Administration, Finance, &...+ Provides timely reports to CUNY MED Dean and Associate Dean of Research that communicate the… more
- Research Foundation CUNY (New York, NY)
- Job Title: Investigator Development Core Manager PVN ID: MD-2410-006531 Category: Research Location: CUNY SCHOOL OF MEDICINE Job Description General Description The ... on primary care and reducing health disparities. As the recipient of a Research Centers in Minority Institutions (RCMI) U54 Cooperative Agreement, CUNY MED has… more