- ICON Clinical Research (Blue Bell, PA)
- Senior Clinical Trial Manager -...crucial role in ensuring the successful delivery of all clinical aspects of the studies . Your expertise and ... clinical development. We are currently seeking a Senior Clinical Trial Manager to...study oversight. + Optimizing Performance: Train and mentor Clinical Research Associates (CRAs) to optimize their performance. +… more
- Stryker (Concord, NH)
- ** Senior Clinical Study Manager (Remote)** Stryker is hiring a Senior Clinical Study Manager to support our Medical Division. In this ... do** + Manage day-to-day operations of one or more clinical studies , ensuring compliance with GCP, FDA...of relevant clinical research experience, preferred in clinical study management. Preferred Qualifications: + Medical… more
- GRAIL (Menlo Park, CA)
- …technology, and healthcare companies. For more information, please visit grail.com . The Senior Clinical Data Manager (CDM) will lead data management ... and we are using the power of next-generation sequencing (NGS), population-scale clinical studies , and state-of-the-art computer science and data science to… more
- Regeneron Pharmaceuticals (Armonk, NY)
- …onsite in one of our locations. Relocation is provided to those who qualify._ The ** Senior Clinical Study Lead** (CSL) is expected to operate with ... trials from study design, through execution, to study close out. The Senior CSL is...studies + Oversees and provides input to the study drug and clinical supplies forecasting, drug… more
- Edwards Lifesciences (Portland, OR)
- …up. **How you'll make an impact:** + As a key member of the Medical Affairs Clinical Science team, the Senior Manager (formal internal title is Senior ... providing scientific expertise throughout the development and implementation of clinical studies and clinical evaluations...for a dynamic portfolio of products across TMTT. The Senior Manager will be an experienced medical… more
- ConvaTec (Lexington, MA)
- …and Convatec's policies and SOPs. **Key Responsibilities:** + Working closely with Clinical Study Managers (CSMs) and Clinical Research Associates ... Clinical Research Organizations (CROs) and other vendors for clinical studies that are outsourced to third...documents such as the protocol, investigator brochure, regulatory documents, clinical study reports and other documents and… more
- BeOne Medicines (San Mateo, CA)
- …Lead and depot PM setting up distribution and return/destruction procedures for studies following the logistics related procedures. + Coordinate drug destruction at ... external audit as needed on logistics data preparation per study or compound level. + Facilitate and coordinate with...Depot vendor's performance and report Depot metrics (KPIs) to senior management. + Ensure the requirements and business process… more
- Bristol Myers Squibb (San Diego, CA)
- …regulatory documents in accordance with ICH, GCP, and company standards including: + Clinical Study Protocols and Amendments + Informed Consent Forms (ICFs) + ... Investigator Brochures (IBs) + Clinical Study Reports (CSRs) + Clinical sections of regulatory submissions (eg, INDs, CTAs, NDAs, MAAs, briefing documents) +… more
- AbbVie (North Chicago, IL)
- …bringing people, process, and technology together to generate business value from clinical trials data. Our operational model is exemplified through execution and ... best in industry resources. This role is on our Study Data Tabulation Model focused team. Responsibilities: + Manage...equivalent. + Must have 8+ years of experience with clinical database design, data loading, and database modeling concepts… more
- HCA Healthcare (Savannah, GA)
- …HCA Healthcare colleagues invested over 156,000 hours impacting our communities. As a Senior Clinical Research Site Manager with Memorial Health University ... vary by location._** Come join our team as a Senior Clinical Research Site Manager ....at the site . Actively engage in tracking of studies conducted at the site . Oversee study… more