- Parexel (Trenton, NJ)
- **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned ... study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and sponsor standards. The...Data Scientist) + May act as a Mentor for Clinical Research Associates **Skills:** + Monitoring Experience:… more
- Parexel (Trenton, NJ)
- The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials ... local country regulations + Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology) +… 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 ... associated with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures timely collection/uploading of… more
- Parexel (Trenton, NJ)
- …Physician in Industry or as a clinical trial investigator with significant clinical research experience The ability to travel 15-20% is required _**Internal ... expanding our esteemed Medical Sciences Team and seeking an Associate /Medical Director to support the growth of our Global...of the projects according to contracted agreement with the sponsor (ie: tasks and time per task contracted) and… more
- Memorial Sloan-Kettering Cancer Center (New York, NY)
- …Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our ... The ideal candidate will be an experienced CMIO (or Associate CMIO) and practicing physician with strong Epic expertise...impact of changes from the distributed build programs. **Non-Epic Clinical Systems, Data, Research and Security** +… more
- IQVIA (Parsippany, NJ)
- …prior monitoring experience. * Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (ie, Good Clinical Practice ... 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)
- …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
- IQVIA (Parsippany, NJ)
- …and owning local trial activites at the regional level._** **Additional Information** Associate Clinical Project Managers (aCPM)/Local Trial Managers are an ... - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements ie ICH GCP and relevant local laws,… more
- IQVIA (New York, NY)
- …bring breakthrough treatments to patients faster._ **Job Overview** We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play ... expectations. Your work will directly contribute to the integrity and quality of clinical research data. **Key Responsibilities** + Conduct all types of site… more
- AbbVie (New York, NY)
- …Description The CRA II advances AbbVie's pipeline by striving for excellence in clinical research , turning science into medicine for patients, and leveraging ... build meaningful, effective engagements that position AbbVie as the sponsor of choice in clinical trials. The... clinical trials. The role focuses on site clinical research by ensuring proper trial conduct,… more
- Fresenius Medical Center (Jersey City, NJ)
- …to act as a resource and provide on-going leadership and support to Clinical Research Assistant I, answering questions and providing assistance as needed ... + Conducts on the job training for Clinical Research Assistant I as requested +...and submitted in a timely manner to Frenova Renal Research , CRO, study sponsor or IRB as… more
- Mount Sinai Health System (New York, NY)
- …position is highly interactive and fast-paced, working closely with the clinical research project management team, Center leadership, operations, administration, ... Director of Operations.** Interested candidates will have experience in academic clinical research settings and familiarity with organizational procedures,… 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
- Bausch + Lomb (Trenton, NJ)
- …established over our 170-year history. We have a significant global research , development, manufacturing and commercial footprint of approximately 13,000 employees ... will serve as a key resource for eye care professionals, applying your clinical expertise and product knowledge to support order fulfillment, resolve issues, and… more
