- Merck & Co. (Rahway, NJ)
- …supply chains. This role works closely with internal stakeholders in the clinical research , procurement, and finance organizations to achieve cross-functional ... ongoing contract management. This role will report to the Associate Director, Clinical Trial Central Labs to...in roles including but not limited to the academic research , pharmaceutical industry, clinical research … more
- Daiichi Sankyo, Inc. (Bernards, 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 an ... and approvals and associated interactions with vendors. Supports regular vendor/ sponsor discussions to identify risks and ongoing study support. Identifies… 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
- 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 ... anticipation of future needs, we are seeking an additional Associate / Medical Director to join Parexel's highly recognized...of the projects according to contracted agreement with the sponsor (ie: tasks and time per task contracted) and… more
- 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)
- …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
- Merck (Rahway, NJ)
- …supply chains. This role works closely with internal stakeholders in the clinical research , procurement, and finance organizations to achieve cross-functional ... ongoing contract management. This role will report to the Associate Director, Clinical Trial Central Labs to...in roles including but not limited to the academic research , pharmaceutical industry, clinical research … more
- System One (Basking Ridge, NJ)
- Title: Associate Director, Epidemiology Analytics 12 month contract Remote - US Based in EST - must be able to come to client site in NJ 1 x quarter Pay Rate $90/hr ... - $93/hr Contracting with this sponsor client offers a strong mix of professional growth,...data management of diverse data (eg, real-world setting and clinical trial) to set up epidemiologic data sets for… 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
- Gilead Sciences, Inc. (Parsippany, NJ)
- …help create possible, together. **Job Description** R&D Quality is seeking an Associate Director, Vendor Quality Management (VQM) to join our high-performing team ... that supports Clinical Development, Pharmacovigilance & Medical Affairs programs at Gilead. In this role you will be responsible for providing quality advice,… more
