- ThermoFisher Scientific (Greenville, NC)
- …of issues in consultation with the Global Medical Indication Lead + Interpret the clinical trial data for regulatory documents (eg CSR, INDs, Annual Reports, ... team, in order to provide reliable, high quality study data within time and budget. **A day in the...years of industry experience required. Experience should be in clinical development in a Pharmaceutical, Biotech or CRO… more
- Otsuka America Pharmaceutical Inc. (Raleigh, NC)
- …day-to-day operations of assigned trial(s), as assigned.** **Participates in ongoing review of clinical trial data focusing on data integrity, trending and ... **Job Summary** Under the direction of the Director/Associate Director of Clinical Management, the Senior Clinical Study Manager is responsible for the oversight… more
- IQVIA (Durham, NC)
- …including timelines, deliverables, and availability of resources. + Collaborate with Data Management, Clinical Development, and Clinical Pharmacologists/PK ... Level:** FSP Senior or Principal Biostatistician for Early Phase Clinical Development (PK) **Location:** Home-based in the US or...**Location:** Home-based in the US or Canada **Why DSSS?** Data Sciences Staffing Solutions, DS3, is a unit within… more
- Otsuka America Pharmaceutical Inc. (Raleigh, NC)
- …to add value strategically. + Provides strategic oversight in our vendor and CRO relationships and provides clinical input into their governance committees. + ... + Working knowledge of associated disciplines, including immunology, biostatistics, clinical pharmacology, formulation science, data management, and medical… more
- Otsuka America Pharmaceutical Inc. (Raleigh, NC)
- …innovations to add value. + Provide strategic oversight in our vendor and CRO relationships and provide clinical input into their governance committees. + ... + Working knowledge of associated disciplines, including immunology, biostatistics, clinical pharmacology, formulation science, data management, and medical… more
- IQVIA (Durham, NC)
- …research programs including review of new business proposals, preclinical and/or clinical data , study protocols, training materials, informed consent, ... study proposals, preparation of training sessions, and interpretation of clinical data , report writing, etc. . Assists... research as study physician/investigator or in the Pharma, CRO , or Biotech industry . Ability to work in… more
- IQVIA (Durham, NC)
- …Provides technical and/or operational support in the delivery and application of industry clinical data standards within the statistical programming data ... with implementing CDISC standards that supports strategies and processes for clinical trials is required.** **Responsibilities:** + Develop, update, and maintain… more
- IQVIA (Durham, NC)
- …database components and theory. + Excellent application development skills. + Strong understanding of clinical trial data and extremely hands on in data ... Programmer + Home Based + Min 7+ years of CRO /Pharma Industry + Therapeutic Areas: Oncology // Immunology //...internal and external clients and (iii) the programming quality control checks for the source data and… more
- IQVIA (Durham, NC)
- …standards of data accuracy and integrity by implementing rigorous quality control processes throughout the data handling and analysis phases. + Demonstrated ... and abilities:** + In-depth knowledge of RWE databases, including large administrative claims data , EMR, disease registries, and clinical trial data . +… more
- IQVIA (Durham, NC)
- …including timelines, deliverables, and availability of resources. + Collaborate with Data Management, Clinical Development, and Clinical Operations ... data derivations. + Performing sample-size/power calculations. + Performing clinical trial simulations. + Performing detailed literature reviews and summarization… more