- Actalent (Pennington, NJ)
- …communication distribution, shipping, filing, tracking, and summarization. + Assist in the clinical trial insurance process by tracking approvals, revisions, and ... skills. Additional Skills & Qualifications + Minimum of an associate 's degree; bachelor's degree preferred. + Previous experience in... Trial Master File systems. + Experience in clinical trial management systems. Pay and Benefits… more
- Mount Sinai Health System (New York, NY)
- …Experience in Phase I-IV clinical studies as a clinical trial assistant or clinical research associate is highly desirable. **Responsibilities** ... Research Associate I monitors all aspects of clinical research trial (s) Clinical study... trial (s) and investigative sites and maintenance of clinical trial master file (CTMF): assures all… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …and authors clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments + Authors and/or reviews documents ... We are seeking a Associate Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the… more
- IQVIA (Parsippany, NJ)
- …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. *… more
- IQVIA (New York, NY)
- …applicable, 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,...required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's… more
- IQVIA (Parsippany, NJ)
- …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. *… more
- Merck (Rahway, NJ)
- …and Word **Preferred Experience and Skills:** + Strong preference for experience with clinical trial specialty services + Experience, either at a sponsor or ... **Job Description** The Associate Director is responsible for defining sourcing strategies... Director is responsible for defining sourcing strategies for Clinical Innovative and Decentralized Services in support of our… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …technical and administrative support to the clinical study team(s) responsible for clinical trial execution. The CSS may be assigned to support the execution ... assignments from the Clinical Study Lead or Clinical Study Associate Manager. The CSS will...plan + Monitors and updates investigator/site status for the trial , and supports with clinical trial… more
- IQVIA (New York, NY)
- …of our client. You will provide peer-to-peer educational dialogue in support of the clinical trial teams. In addition, you will ensure compliant and high-quality ... **MSL Associate Director** We are excited to announce that...area (hepatology and/or infectious diseases) experience highly preferred + Clinical trial experience preferred. + Valid driver's… more
- Merck (Rahway, NJ)
- …Engineering or related field plus 9 years SAS programming experience in a clinical trial environment. + MS in Computer Science, Statistics, Applied Mathematics, ... plus 7 or more years SAS programming experience in a clinical trial environment. **Department Required Skills and Experience:** + Excellent interpersonal skills… more
- Bristol Myers Squibb (Princeton, NJ)
- …aligned medical communications plans; adjust communications plans in accordance with clinical trial results/milestones and changes in the healthcare landscape ... Professional (CMPP), and ISMPP active member highly desired + Understanding of clinical trial design and execution, statistical methods and clinical… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …and may author clinically relevant sections and review other scientific portions of clinical trial protocols and amendments + Assists with and may author/review ... process, regulatory requirements and ICH/GCP guidelines. Proven track in clinical trial process improvements. Considerable organizational awareness, including… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director, RBQM - HOCT, ICN will mainly be responsible for developing ... effective risk and issue management. Provide quality and compliance consultation to clinical trials teams throughout study lifecycle and establish a feedback loop to… more
- Merck (Rahway, NJ)
- …Engineering or related field plus 9 years SAS programming experience in a clinical trial environment + MS in Computer Science, Statistics, Applied Mathematics, ... plus 7 or more years SAS programming experience in a clinical trial environment **Department Required Skills and Experience:** + Excellent interpersonal skills… more
- Merck (Rahway, NJ)
- …+ Develop model-based strategies (translational PK/PD strategies, mechanistic, popPK/PD, clinical trial simulations, etc.) for quantitative analyses, within ... / Rahway, NJ is seeking a curious and collaborative Associate Director to support our robust infectious disease and...including, but not limited to translational strategies, dose selection, clinical trial design, and go/no-go decisions. +… more
- Merck (Rahway, NJ)
- …engagers, bispecifics) in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial ... and Pharmacometrics -** **Immune/Oncology** **(QP2-IO)** team in the role of Associate Director, Quantitative Systems Pharmacology (QSP). QP2-IO team is part of… more
- Mount Sinai Health System (New York, NY)
- …resources as needed. **Research duties include:** + Identifying patients eligible for clinical trial participation + Participating in research in conjunction ... the Mount Sinai Health System is recruiting a physician associate to serve as the manager of clinical... associate to serve as the manager of clinical care for the Pancreatic Multidisciplinary Program under the… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Associate Statistical Project Leader **Location:** Morristown, NJ, Cambridge, MA **About the Job** Are you ready to shape the future of medicine? The ... teams accelerate progress. Join our **Biostatistics Immunology & Inflammation (I&I) as Associate Statistical Project Leader** and you will lead several I&I phase 2… more
- Bristol Myers Squibb (Princeton, NJ)
- …DSURs, etc. + Co-lead the cross-functional rapid response teams to respond to Clinical Trial Application (CTA) queries on new protocols and protocol amendments ... and in their personal lives. Read more: careers.bms.com/working-with-us . ** Associate Director, Global Regulatory Strategy, Neuroscience** **Position Summary:** The… more
- Bristol Myers Squibb (Princeton, NJ)
- …6 years of experience. Experience must include the following: + knowledge of clinical trial + postmarketing safety + marketing authorization filing and ... Lead Safety Data Review (SDR) Teams in the review and evaluation of clinical data to support signal detection. Specially, this position will perform the following… more