- Merck & Co. (Rahway, NJ)
- …(Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the ... clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications,...percent of the time to manage future or ongoing clinical research projects.Qualifications Education MD or MD/Ph.D.Required… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …with minimal direction from group head and provide statistical scientific leadership for clinical trial safety data. Lead the statistical support for safety ... Safety analysis methodology and standardizationDevelop and support statistical safety analysis methodology and standardization across the clinical … more
- Eisai, Inc (Nutley, NJ)
- …related technical and end user support to other areas of Data Operations, Data Management, Clinical Safety Data Review and Clinical team. The Assoc. Director ... in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of...your profile, we want to hear from you. The Associate Director, Clinical Programming must have expertise… more
- Merck & Co. (Rahway, NJ)
- …enhance performance.Maintain a strong focus on compliance and Environmental Health and Safety (EHS) to drive supply excellence.Serve as the primary technical contact ... to resolve manufacturing challenges and minimize supply disruptions.Collaborate with Research Laboratories groups during New Product Introductions/Technical Transfers and… more
- Merck & Co. (Durham, NC)
- …the Master Data team with general Material Handling Steward tasksDrive safety , quality and process enhancements throughout the supply chain - Project ... and frozen storage needs/capacity.Collaborate with EHS team to ensure all departmental safety and training requirements are met, related to any new project… more
- Merck & Co. (Rahway, NJ)
- …biologics, vaccine) Drug Product development and Good Manufacturing Practice (GMP) clinical supply manufacturing facility in Rahway, New Jersey.The Sterile Process ... Engineer role at the Associate Director level will leverage the individual's leadership, technical,...and communication skillsets to drive the success of our clinical manufacturing facility and organization. As the facility is… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …CSPV to enable/effectively support safety signaling detections and across compounds safety reviews (ie, ILD). Collaborate with Clinical Development and ... primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Summary: The purpose… more
- Eisai, Inc (Exton, PA)
- …is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, ... your profile, we want to hear from you. The Associate Director of Biologics Operations Upstream and Downstream is...in development through their lifecycle (Preclinical through phase III clinical development) at the Biologics Pilot Plant as well… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …drug coding conventions (MedDRA, WHO-DD). preferredExtensive knowledge of FDA regulations, clinical and safety databases, preferredFamiliarity with Good ... primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Job Summary: This… more
- Merck & Co. (North Wales, PA)
- …including data steps, procedures, SAS/MACRO, SAS/GRAPH and programming expertise with clinical endpoint data (efficacy and safety ) and pharmacokinetic data ... programming requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data, transform the data into… more
- Merck & Co. (Rahway, NJ)
- …diversified portfolio of prescription medicines, vaccines, and animal health products. Our Research Scientists are our Inventors. We identify and target steps in ... global healthcare. The Biologics and Biopharmaceutics team is responsible for the research and development of sterile & parenteral drug products for biologics… more
- Merck & Co. (Rahway, NJ)
- …GMP (Good Manufacturing Practices) manufacturing facility in the Small Molecule Process Research and Development (SM PR&D) organization. The SSO pilot plant enables ... on assistance for daily production activities while ensuring compliance with Safety & Environmental (S&E) and current Good Manufacturing Practices (cGMPs)… more
- Merck & Co. (Rahway, NJ)
- …GMP (Good Manufacturing Practices) manufacturing facility in the Small Molecule Process Research and Development (SM PR&D) organization. The SSO pilot plant enables ... on assistance for daily production activities while ensuring compliance with Safety & Environmental (S&E) and current Good Manufacturing Practices (cGMPs)… more
- Eisai, Inc (Phoenix, AZ)
- …decision-makers through understanding of issues and opportunities in territory. Deliver clinical , efficacy, and safety messaging and information about product ... is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines,… more
- Cedars Sinai (Los Angeles, CA)
- …improving patient outcomes. Are you ready to be a part of breakthrough research ? The Clinical Research Associate I works directly with a Clinical ... and research objectives. Responsible for completing case report forms, entering clinical research data, and assist with regulatory submissions to the IRB.… more
- Cedars Sinai (West Hollywood, CA)
- …investigation. To learn more, please visit: MIRIAD IBD Biobank & Database | Cedars-Sinai. The Clinical Research Associate I works under the direction of a ... Clinical Research Coordinator, Research Program Administrator, ...including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines.… more
- Arrowhead Pharmaceuticals (San Diego, CA)
- …who are collaborating to bring new therapies to patients in need. The Position The Clinical Research Associate (CRA) provides support to Study Lead(s) in ... 2 years in clinical research 2 years as a Clinical Trial Associate ; study coordinator Proficient knowledge and understanding of ICH-GCP Excellent… more
- Mount Sinai Hospital (New York, NY)
- Job Description The Clinical Research Associate I monitors all aspects of clinical research trial(s) Clinical study life-cycle responsibilities ... clinical study for the identification and evaluation of safety issues and any patterns that are identifiable. Reports...studies as a clinical trial assistant or clinical research associate is highly… more
- Pennsylvania Medicine (Havertown, PA)
- …mission of providing the highest level of care to patients, conducting innovative research , and educating future leaders in the field of medicine. Working for this ... leading academic medical center means collaboration with top clinical , technical and business professionals across all disciplines. Today at Penn Medicine, someone… more
- Dana-Farber Cancer Institute (Boston, MA)
- …with activity completed. Qualifications Bachelor's Degree or 1 year of Dana-Farber Associate Clinical Research Coordinator experience required. 0-1 years ... Early Detection and Interception of Blood Cancers seeks a Clinical Research Coordinator to assist in the...to monitor visits, external site enrollment, amendments, receipt of Safety Reports, etc. into Clinical Trial Management… more
