- Novo Nordisk Inc. (Plainsboro, NJ)
- …of clinical trials improvement/innovation projects for NACD and Novo Nordisk (eg, clinical trial site staff, clinical research vendors). Manages ... Development (NACD) goals, including successful delivery of studies within the clinical trial portfolio. Contributes to local or increasingly complex… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …of clinical trials improvement/innovation projects for NACD and Novo Nordisk (eg, clinical trial site staff, IRBs, clinical research vendors). ... risk identification and mitigation planning for assigned clinical trial sites Drives and tracks site activation and start-up activities with clinical … more
- Novo Nordisk Inc. (San Antonio, TX)
- …of clinical trials and improvement/innovation projects for NACD and Novo Nordisk (eg, clinical trial site staff, clinical research vendors). Manages ... Development (NACD) goals, including successful delivery of studies within the clinical trial portfolio. Contributes to local or increasingly complex… more
- Merck & Co. (Rahway, NJ)
- …CRM.Attend local Investigator Meetings if requested to.Interface with GCTO partners on clinical trial execution.Escalates site performance issues to CRM ... clinical trials. Under the oversight of the Clinical Research Director (CRD) or Head of Site...these guidelinesExpertise in and excellent working knowledge of core trial management systems and tools Behavioral Competency Expectations: High… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- … contracts, budgets, site payment and related reporting including global clinical trial financial transparency and Medicare, Medicaid, and SCHIP Extension ... practices.Lead GCO process improvement initiatives for the global reporting of GCO clinical trial spend. Financial Transparency (FT) and MMSEA Reporting… more
- Merck & Co. (Rahway, NJ)
- …new medicines to patients. The key areas of focus include: (1) diversity in clinical trials, (2) clinical trial recruitment and (3) general education ... enterprise wide (Internal and External) critical communications, focused on our global Clinical Trial efforts.This role is responsible for supporting the… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …activities in collaboration with the CRO and the study team. Oversee the site qualification process.Monitor clinical trial performance and quality metrics ... disorders. Summary The incumbent will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions, in adherence to Good … more
- Merck & Co. (North Wales, PA)
- … Clinical Safety StatisticsInteract with Safety Physicians, Safety Scientists, Clinical Trial Physicians , Regulatory, Early/Late Development Statistics, ... project management skills. --Good understanding of worldwide regulatory requirements and clinical trial expertise .Strong oral and written communication skills.… 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
- Merck & Co. (Rahway, NJ)
- …translational PK/PD approaches, population pharmacokinetic models, exposure-response models, clinical trial simulation, disease progression models, quantitative ... and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial applications… more
- Merck & Co. (Rahway, NJ)
- …or Master's plus minimum 7 years SAS programming experience in a clinical trial environmentExperience leading large and/or complex statistical programming ... Job DescriptionThe Associate Principal Programmer leads the statistical programming activities...to quality, compliance and timeliness requirements.-Expertise in SAS and clinical trial programming including data steps, procedures,… more
- Merck & Co. (North Wales, PA)
- …of 9 years Statistical Analysis System (SAS) programming experience in a clinical trial environment. MS (preferred) in Computer Science, Statistics, Applied ... of 7 years Statistical Analysis System (SAS) programming experience in a clinical trial environment. Required Experience and Skills: Experience leading large… more
- Merck & Co. (Rahway, NJ)
- …(popPK), PK/PD models, exposure response (ER) models, model-based meta-analysis (MBMA), clinical trial simulations (CTS) and disease progression modeling into ... our company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas.This...seek to improve cycle time, cost/size, number of trials, clinical trial design and Go/No Go decisionsFraming… 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
- Catalent (San Diego, CA)
- …and performance of line clearances in a Class 100,000 environment, maintenance of clinical trial material inventory logs;Duties include but not limited to ... Quality Assurance Associate II - Manufacturing Catalent Pharma Solutions in...manufacturing and stability storage and testing as well as Clinical Supply Services. At Catalent San Diego, we recruit… more
- Merck & Co. (North Wales, PA)
- …or related field plus 9 years SAS programming experience in a clinical trial environment.MS in Computer Science, Statistics, Applied Mathematics, Life ... 7 or more years SAS programming experience in a clinical trial environment. Department Required Skills and...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… more
- DivIHN Integration Inc (San Diego, CA)
- …please contact one of our Talent Specialists Sivanesan at 224 369 0756 Title: Clinical Trial Assistant (CTA) Location: San Diego, CA Duration: 12 Months ... with biological specimens and data sets, ideally with some clinical trial familiarity Will be providing general...and internal tracking systems. To assist in tracking of clinical studies and site related purchase orders,… more
- Insmed Incorporated (Bridgewater, NJ)
- … Director of Biostatistics is responsible for the statistical aspects for complex clinical trial (s) or indication product line. This role leads the protocol ... section development, study setup, execution, analysis, and reporting of clinical trials, and interacts with cross-functional teams.ResponsibilitiesAdditional representative responsibilities… more
- Arthrex (Naples, FL)
- …, biomaterials and biomechanical professionals. Arthrex is actively searching for an Associate Clinical Study Manager to join the Orthopedic Research department. ... development is preferred.Machine, Tools, and/or Equipment Skills:Experience in Microsoft Office, Clinical trial Electronic Data Capture systems, is required.… 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...Will this job require the employee to work on site ? No Employee Onsite Status Hybrid Telework: Required Background… more
