- 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
- IQVIA (Parsippany, NJ)
- …is required, Nursing experience in addition to this is ideal!_ **Job Overview** Associate Clinical Project Managers (aCPM)/Local Trial Managers are an ... integral part of clinical trial delivery, liaising with clinical teams to improve patients' lives by bringing new drugs to the market faster. The aCPM is a… more
- Merck (Rahway, NJ)
- …Documentation, Clinical Investigations, Clinical Judgment, Clinical Reporting, Clinical Research, Clinical Trial Documentation, Clinical ... **Job Description** The Associate Vice President (AVP)/Section Head, Global Clinical Development, Pediatrics will focus on driving strategy, development, and… 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 (Parsippany, NJ)
- …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
- Bristol Myers Squibb (Princeton, NJ)
- …projects * Efficiently plans, coordinates, and delivers complete, high quality and reliable clinical trial data in a timely manner for assigned projects * ... BMS R&D pipeline. This role may report into Director, Clinical Data Management or Associate Director, ...functional study team members to ensure on-going review of trial data currency, quality and completeness * Represents DM… 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)
- …+ Develop model-based strategies (translational PK/PD strategies, mechanistic model, POPPK/PD, clinical trial simulations, etc) for quantitative analyses, within ... / Rahway, NJ is seeking a curious and collaborative Associate Director to support our rapidly expanding cardiometabolic and...drug development including, but not limited to dose selection, clinical trial design, and go/no-go decisions. +… 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
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- … Director/Director). + An advanced understanding of drug development principles and clinical trial implementation, management and reporting are essential and ... **Job Description** Otsuka is seeking a Director, Global Clinical Development (GCD), who will be responsible for the design and oversight of clinical research… 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
- 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
- IQVIA (Parsippany, NJ)
- …legal, financial and/or technical writing skills. * Strong understanding of regulated clinical trial environment and knowledge of drug development process. * ... regulatory requirements, SOPs and company's Corporate Standards. * Good understanding of clinical trial contract management. * Ability to develop and suggest… more
- Sumitomo Pharma (Trenton, NJ)
- …marketed products. + Conduct safety surveillance over product life cycle, reviewing clinical trial and post-marketing Individual Case Safety Reports (ICSRs), ... highly motivated, and experienced individual for the position of ** Associate Medical Director.** The Associate Medical Director...safety of clinical trials, including monitoring of clinical trial safety and laboratory data. +… 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
- 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