- Insmed Incorporated (Bridgewater, NJ)
- …and collecting TMF status updates and TMF metricsParticipates in the review of clinical trial agreements, CRO and vendor contractual documents, work orders, and ... review, processing and timely payment execution of invoices related to clinical trial agreements and CRO/vendor Scopes of work and contract terms.Assists with… more
- Merck & Co. (North Wales, PA)
- …is to lead the coordination and execution of major change projects across Global Clinical Trial Operations. The role will also assist with Program Management ... are updated and readily available for internal teams and senior leaders. Upon completion of a project, the PMO...degree with at least nine (9) years of pharmaceutical, clinical drug development, project management and/or medical field experience.… more
- Merck & Co. (Rahway, NJ)
- …and ensures continuity of site relationships through all-phases of the trial .-Performs clinical study site management/monitoring activities in compliance with ... site contact and site manager throughout all phases of a clinical research study,-taking overall responsibility of allocated sites.Actively develops and expands… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …submission documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to ... Planning and Execution: Provides input on major milestones of trial , clinical trial plan and...CRO / vendors / AROAdditional non-study related activities: Occasional senior management interactions at FIHC, WDC; Initiates contact w/KOL… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and ... clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good … more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …business, and other functional groups across NN. External relationships can include clinical trial sites and external vendors. Essential Functions Develop and ... escalating quality concerns. Relationships This position reports to the Associate Director of GXP Oversight and/or Head of GXP...or resolve, for example across various topics, such as clinical trial management, deviation handling, and product… more
- Merck & Co. (Boston, MA)
- … pharmacology, biomarkers of target engagement, experimental medicine platforms, early clinical trial designs and conduct, and operational understanding for ... Job DescriptionThe Associate Vice President (AVP)/Therapeutic Area Head, Immunology Translational Medicine, will be responsible for leading the Translational… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …study findings through presentations and/or publications in peer-reviewed scientific journalsAssess clinical trial and/or other data sources to contextualize ... areas centered around rare diseases and immune disorders. SUMMARYThe Associate Director, Pharmacoepidemiology position provides epidemiologic, methodological, and analytic… more
- Merck & Co. (North Wales, PA)
- …support for anticipated promotional messages and claims (aligned with marketing strategy) in clinical trial design and product labeling as it relates to the ... Job DescriptionReports to the Director/ Senior Director in the Office of Promotion and...in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the review and approval… more
- Merck & Co. (Rahway, NJ)
- …business.Under the guidance of the Clinical Development Finance Associate Director, the Finance Senior Specialist will:Provide financial planning, ... with stakeholders including the Global Project Manager, Global Trial Manager, Clinical Sub Team, Clinical Trial Team and Outsourced Trial Team for… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... and field alignment directors. They will also be the senior strategic representative of medical affairs in the relevant...clear direction on Medical Affiars engagement needs to the clinical data science & evidence team and other relevant… more
- George Washington University (Washington, DC)
- …University of Virginia and numerous clinical providers in Washington, DC. The Senior Research Associate will lead the day-to-day management of the study and ... Health at the George Washington University is seeking a Senior Research Associate to assist the department... clinical aspects of HIV disease Experience with clinical trials or efficacy trial conduct Experience… more
- Integrated Resources, Inc (Cambridge, MA)
- Job Title: Senior Drug Safety Specialist Location: Cambridge, MA Duration: 8+ Months Job Description: Duties: . Reporting to the Associate Director, Drug Safety ... role in drug safety activities, supporting records management and compliance across the clinical development and marketing programs. You will be a key contributor to… more
- Integrated Resources, Inc (West Sacramento, CA)
- …processing. * Delight customers and accurately resolve issues. * Primary customer contact for clinical , pharma and clinical trial testing. * Ensure all ... Job Title: Associate Project Manager Location: West Sacramento, CA, 95605...a complaint log documenting any customer issues and notify senior leadership of all perceived issues and complaints. *… more
- George Washington University (Washington, DC)
- …to redefine hemoglobin reference values used to diagnose anemia in pregnancy and a clinical trial to assess the optimal supplemental dose of vitamin B12 in ... I. DEPARTMENT INFORMATION Job Description Summary: Postdoctoral Associate position is in Maternal Nutrition Clinical...the approval of the department head and may require senior officer approval. Appointments are usually for not less… more
- George Washington University (Washington, DC)
- …maintaining standard operational efficiencies. Duties and Responsibilities: Works with the clinical trial management system - OnCore. Oversees all communication ... and Research Administration, is recruiting for a Research Program Associate to work in a dynamic and growing translational...to work in a dynamic and growing translational and clinical research environment. . In order to support the… more
- Bausch + Lomb (Rochester, NY)
- …of eye health in the future. **Objectives** Under the supervision of the Director, Clinical Operations / Sr. Clinical Trial Manager, responsible for ... all applicable regulations. Under the supervision of the Director, Clinical Operations / Sr. Clinical Trial...of the Director, Clinical Operations / Sr. Clinical Trial Manager, responsible for supporting the… more
- Boehringer Ingelheim (Ridgefield, CT)
- **Description** The Senior Associate Director, Clinical Trial Diversity supports the Clinical Development & Operations (CD&O) strategy for Diversity ... developing goals and strategies for diverse patient enrollment. The Senior Associate Director monitors progress intervenes as...the development and execution of Diversity & Inclusion in clinical trial strategies, core processes and best… more
- Lilly (Indianapolis, IN)
- …Assurance (QA) is responsible for providing quality oversight of all materials used in clinical trials. PRD QA Clinical Trial (CT) Packaging is responsible ... for global packaging operations and provide on-going Quality oversight to outsourced Clinical Trial Packaging activities. The Packaging CP Oversight role is… more
- Merck (Columbus, OH)
- …is to lead the coordination and execution of major change projects across Global Clinical Trial Operations. The role will also assist with Program Management ... are updated and readily available for internal teams and senior leaders. Upon completion of a project, the PMO...degree with at least nine (9) years of pharmaceutical, clinical drug development, project management and/or medical field experience.… more
