- IQVIA (Raleigh, NC)
- …Management & Monitoring staff in the initiation, oversight, and follow-up of clinical studies . This is done in a strictly scientific, non-promotional manner, and in ... the initiation and conduct of prioritized Company clinical trials. + Supports clinicals study sites with knowledge and training on the disease, the treatment, the… more
- United Therapeutics (Raleigh, NC)
- …advocacy function at various internal cross-functional team meetings + Provide study recruitment support and patient partnership + Enhance patient recruitment for ... research including clinical trials, medical affairs studies , HEOR studies , qualitative research, and human factors studies + Identify opportunities for… more
- IQVIA (Durham, NC)
- …The Principal Biostatistician is responsible for providing statistical support for drug development programs in early phases. **Additional Benefits:** + Home-based ... to establish project timelines. + Provide statistical input to study protocols. + Writes the statistical sections of clinical...is PREFERRED.** + Experience to help with dose escalation studies , efficacy endpoints and solid tumor. + 1+ years… more
- Alaka'ina Foundation Family of Companies (Camp Lejeune, NC)
- …+ Responsible for coordinating the research activities of assigned IRB-approved study protocols. Work is evaluated by observation and outcomes for effectiveness ... patients through a research protocol, maintaining and document contact with study subjects and research personnel from government agencies, granting agencies,… more
- Otsuka America Pharmaceutical Inc. (Raleigh, NC)
- …Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and drug product at CDMOs + Design and lead ... method validation and implementation activities for drug substance and drug product ensuring compliance with relevant ICH and regulatory guidelines + Develop and… more
- Otsuka America Pharmaceutical Inc. (Raleigh, NC)
- …**pharmacometrics** studies , while providing input into all phases of drug development including, but not limited to dose finding, dose optimization, ... phase assets. **Job Description** + Conduct **pharmacometrics** activities related to study design, protocol development, study execution, reporting and… more
- Veterans Affairs, Veterans Health Administration (Fayetteville, NC)
- …in a testing designated position are subject to urinalysis to screen for illegal drug use prior to appointment. Applicants who refuse to be tested will be denied ... of the requirements below: (1) Successful completion of a full four-year course of study from an accredited college or university, leading to a bachelor's or higher… more
- IQVIA (Durham, NC)
- …Biostatistician is responsible for providing full range statistical support for drug development based on real world evidence (RWE). **Additional Benefits:** + ... as statistical lead and represents Biometrics on health outcomes and epidemiology studies . + Serves as subject matter expert for RWE/HEOR/HTA research design,… more
- ICON Clinical Research (Winston Salem, NC)
- …promotes the mission of Accellacare, and strives to meet and exceed study priorities. This individual is responsible for recruiting and promoting our service ... the Sr CRC will perform tasks required to coordinate and complete a study according to the protocol._ **Duties:** + Performing technical and clinical requirements of… more
- Fujifilm (Raleigh, NC)
- …needs and assist with the development and implementation of clinical studies and education solutions. Additionally, this role builds and nurtures relationships ... with clinical customers as it relates to participating in clinical studies and broader collaboration with the marketing organization. The incumbent is responsible… more