- 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 ... will be responsible for ensuring the delivery execution of clinical studies in one or more geographic...US and abroad, governmental, academic, community and industry organizations.The Senior Clinical Study Manager role… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Clinical Director (Sr. Principal Scientist) has primary responsibility for the strategic planning and directing clinical research ... in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire...safety and efficacy as well as new drug applications, clinical study reports, or publication; andParticipation in… more
- Merck & Co. (Rahway, NJ)
- …Respiratory projects, including pipeline candidates and licensed productsSupervises development of clinical documents including protocols, clinical study ... Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical...development of assets within the Respiratory Section of Global Clinical DevelopmentMay serve as a senior therapeutic… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and Modeling and Simulation plans, design and lead study teams to execute Clinical Pharmacology studies , conduct hands on population PK and PKPD analyses and ... documentsServes as a specialist in PK-PD and Pop PK-PD concepts, phase 1-4 clinical studies , literature, and regulatory guidelines and can conduct/develop PK-PD… more
- Merck & Co. (North Wales, PA)
- …The Senior Director will manage the entire cycle of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, ... talented and dedicated colleagues while developing and expanding your career.The Senior Clinical Director (Sr. Principal Scientist) has primary responsibility… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …position, task oriented in the execution of processes, as directed by senior staff, playing a supportive role in ensuring adherence to Project objectives, ... vendors. Supports regular vendor/sponsor discussions to identify risks and ongoing study support. Identifies critical issues which may compromise patient dosing or… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …KPIs, KRIs, KQIs across all RD LFs. Define Cycle Times, Identity key milestones at Study , Country, and Site Level to gauge clinical trial performance. Build and ... and roles. Candidate will be responsible for managing external Benchmarking Study Submissions and seeking out external competitive intelligence to provide line… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …indications.Support as medical lead for select company-sponsored GMA evidence generating studies /projects. Manages all medical aspects such as study document ... research areas centered around rare diseases and immune disorders. Summary The Associate Director Global Medical Affairs Oncology (GMA), under the direction of the… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …requirements for diagnostics and devices.Provide strategic input on key development documents, clinical protocols, study reports, IBs, INDs, CTAs, IDEs, SRDs, ... dossier documents for submissions globally. Ensure high quality collaboration with Clinical Biomarker and Companion Diagnostics team for development of biomarker,… more
- Novo Nordisk Inc. (Durham, NC)
- …May consider an Associate 's degree in chemistry or relevant field of study from an accredited university with a minimum of three (3) years of experience ... & processes in accordance with relevant project plans & timelines. Relationships Senior Manager, Quality Control - OFP. Essential Functions Accuracy & Scientific… more
- Eisai, Inc (Nutley, NJ)
- …and Analytics plus 2 years of work experience in job offered or as Senior Systems Analyst/Data Analyst/ Associate Projects. Also requires 2 years of experience ... from you.Application Programmer sought by pharmaceutical company in Nutley, NJ.Support clinical applications for clinical data management. Perform data review… more
- University of Maryland, Baltimore (Baltimore, MD)
- *The University of Maryland, Baltimore*(UMB) is seeking a*Corporate & Clinical Trials Contracts Senior Associate * in the Center for Clinical Trials and ... **Reg or CII Exempt Staff* **Organization:** **Research and Development - Center for Clinical Trials* **Title:** * Senior Associate , Clinical Trials… more
- Catalyst Clinical Research LLC (Raleigh, NC)
- …pancreatic or advanced solid tumor? We have a role for you! Job Duties: As a Senior Clinical Research Associate , you will monitor clinical trial programs ... study sites. + Effectively communicates with site study staff and Catalyst clinical research personnel...Field Monitor from the assigned Clinical Trial Associate . + Works closely with the extended study… more
- Boehringer Ingelheim (St. Joseph, MO)
- …and benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Senior Clinical Research Associate (SCRA) conducts in-house and ... these duties for on-site and off-site (national and global) clinical studies and trials for all animal...drafts protocols and reports and can act as a Study Leader for studies . The SCRA is… more
- The Mount Sinai Health System (New York, NY)
- The Senior Clinical Research Associate manages all aspects of clinical research trial(s) coordination including activities involved in the planning, ... conduct and completion of a clinical trial(s) at multiple sites. Depending on the department and clinical trial there may be significant travel time required.… more
- Philips (Pittsburgh, PA)
- …and qualification, and initiation. As well, developing the monitoring plan for clinical studies . + Acting as Clinical Study Manager for designated ... **Your role:** + Owning the overall study process and adherence to clinical ...+ You've acquired 5+ years of experience as a Senior Clinical Research Associate , conducting/executing… more
- Lilly (IN)
- …in the study planning, execution, and close out activities of clinical studies . + Proactively identifies potential technical and operational issues/risks and ... Clinical Data Associate , Clinical Data Management Associate to deliver study database per business need and before first patient visit + Comply with… more
- Lilly (IN)
- …California; South San Francisco, California; Stamford, Connecticut; and Madrid, Spain. The Clinical Data Analytics Associate is responsible for programming and ... testing, data technology, data flow, and data standards. The Clinical Data Analytics Associate collaborates with the...standardized reports, dashboards and innovative analytics for use in study deliverables for global clinical trials. The… 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 ... Societies). + Accountable for optimal planning, interpretation and data presentation of clinical studies from FIM throughout pivotal studies , ensuring… more
- WuXi AppTec (Austin, TX)
- …position within the Operations team and is assigned as a study lead to manage clinical trial studies . The Senior CRA will partner with a Project Manager ... every disease can be treated." **Responsibilities** **Job Summary:** The Senior Clinical Research Associate is...teams, liaise with other functional areas to accurately coordinate clinical study activities + Coordinate clinical… more
