- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …(FDA) regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines.The Senior Clinical Study Manager will have routine interaction ... in the US and abroad, governmental, academic, community and industry organizations.The Senior Clinical Study Manager role is primarily a tactical study… 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
- 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)
- …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
- 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)
- …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
- 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
- Vera Therapeutics (Brisbane, CA)
- Title: Clinical Trial Manager Associate Location:...Summary: The Clinical Trial Manager Associate will report to the Senior Director, ... databases, spreadsheets, and other study tools * Serve as a back up to the Clinical Trial Manager and team * May lead a component of a routine clinical … 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
- Ascension Health (Carmel, IN)
- …**Additional Preferences** Ascension St. Vincent is looking for an **RN** - ** Clinical Trial Research Coordinator.** Minimum requirements: The right candidate ... have their **Indiana RN** license with Cardiology experience and Clinical Trial Research experience. **The areas of...of care, including more than 140 hospitals and 40 senior living communities in 19 states. Our Mission, Vision… more
- University of Southern California (Los Angeles, CA)
- …the design and development of investigator-initiated trials (IIT) and their required clinical trial databases. The investigator-initiated clinical trial ... documents for clarity and consistency, and management of the clinical trial database design and implementation. The...person will also work closely with CISO Director and Associate Director in ensuring optimal support for IIT development… more
- Catalyst Clinical Research LLC (Raleigh, NC)
- As a Senior Clinical Research Associate with...is provided to the Field Monitor from the assigned Clinical Trial Associate . + Works closely ... strong Car-T/Cell therapy experience, you will monitor clinical trial programs and manage regional clinical trial sites to support biological and… more
- Abbott (Alameda, CA)
- …+ Must have 3+ years of relevant experience in site monitoring, clinical trial practices and regulations. **Preferred Qualifications** + Demonstrated excellence ... working mothers, female executives, and scientists. **The Opportunity** The Senior CRA will assist in the clinical ...management. + Solid understanding and demonstrated experience of the clinical trial process including study design and… more
- Boehringer Ingelheim (Ridgefield, CT)
- **Description** The role of Senior Clinical Program Leader (CPL) - Retinal health, assumes full medico-scientific and strategic leadership of clinical ... and other contributors), Clinical Development Plans or similar documents, Core Clinical Trial Protocols, including the CTP strategy and core CTP elements… more
- WuXi AppTec (Austin, TX)
- …can be made and every disease can be treated." **Responsibilities** **Job Summary:** The Senior Clinical Research Associate is a critical position within the ... and is assigned as a study lead to manage clinical trial studies. The Senior ...Education:** + Minimum of 4 years experience as a Clinical Research Associate in the pharmaceutical/biotech or… more
- Boehringer Ingelheim (Athens, GA)
- …benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Senior Clinical Research Associate (SCRA) supporting Environmental Fate ... for tracking timelines and deliverables and interfacing with internal collaborators (eg, clinical trial supply, data management, regulatory affairs, PV). The… more
- United Therapeutics (Durham, NC)
- …reports); Oversee database generation and production of tables and listings; Ensure clinical trial material (CTM) is available for sites and/or Contract ... + Demonstrated understanding of the overall drug development process with clinical trial design, study implementation, sponsor/site interactions, scientific and… more
- Lilly (IN)
- … Data Analytics Associate is responsible for programming and testing clinical trial data reports/listings, dashboards and analytics. This requires an in ... testing, data technology, data flow, and data standards. The Clinical Data Analytics Associate collaborates with the...and test data reporting, dashboarding and analytics for a trial or set of trials within a program using… more
- Lilly (IN)
- … Clinical Study Build Programmer is responsible for programming and testing clinical trial data collection databases, including the mapping, testing and ... collection systems and associated data repository mappings for a trial or set of trials within a program using...Partner with Data and Analytics colleagues such as the Clinical Data Associate , Clinical Data… more
