- Merck & Co. (Rahway, NJ)
- …The Specialist will be responsible for: Authoring scientifically valid clinical trial registration and results postings on www.ClinicalTrials.gov (United ... development portfolio and compliance in public disclosure of clinical trials and their results, document disclosure,...Specialist may occasionally prepare plain language (lay) summary trial results at a 6-8th grade reading level and… more
- Eisai, Inc (San Francisco, CA)
- …state, product prescribing information, approved promotional clinical trials , patient access to medication, and regulatory /compliance guidelines.Strong ... want to hear from you. Job Summary The Senior Oncology Sales Specialist is responsible for meeting/exceeding sales goals through promoting Oncology therapeutic… more
- Eisai, Inc (Louisville, KY)
- …state, product prescribing information, approved promotional clinical trials , patient access to medication, and regulatory /compliance guidelines.Strong ... want to hear from you. Job Summary The Senior Oncology Sales Specialist is responsible for meeting/exceeding sales goals through promoting Oncology therapeutic… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …time to accelerate and expand that transformation. At Legend Biotech, we are excited to bring clinical trials to patients in our pursuit of a cure. While we are ... OverviewThe QC Technician is responsible for QC sample labelling process. The QC Specialist is encouraged to work independently on routine tasks and have conceptual… more
- University of Pennsylvania (Philadelphia, PA)
- …of health and wellness programs and resources, and much more. Posted Job Title Clinical Research Regulatory Specialist B (Abramson Cancer Center) Job Profile ... Title Clinical Research Regulatory Specialist B Job Description Summary The...regulatory aspects of the initiation of Phase I-V clinical trials with a focus on required… more
- University of Southern California (Los Angeles, CA)
- … SpecialistApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ Clinical -Research- Regulatory - Specialist ... information pertinent to studying milestone progress, including but not limited to: clinical trial management systems, IRB databases, internal and external… more
- Baylor Scott & White Health (Plano, TX)
- ** Clinical Research Regulatory Specialist ** **The Heart Hospital** **Plano, TX** **JOB SUMMARY** The Clinical Research Regulatory Specialist ... to research involving human subjects. This position also provides regulatory guidance and direction to internal clinical ... requirements are met, to include ensuring requirements for trial registration, results and reporting are completed in a… more
- Methodist Health System (Dallas, TX)
- … clinical , investigator initiated trials (IITs), and retrospective analysis of clinical data. The Regulatory Specialist will support the mission, ... requirements * Obtain and facilitate tracking of relevant regulatory documents for clinical trials ...trials assigned. * Assist in the development of clinical trial documents for signature of principal… more
- University of Pennsylvania (Philadelphia, PA)
- …Title Veeva Quality Assurance Specialist (Abramson Cancer Center) Job Profile Title Clinical Research Regulatory Specialist B Job Description Summary The ... is a world leader in developing and conducting innovative clinical trials for the prevention, diagnosis, and...CRU Regulatory Affairs Office seeks a full-time Regulatory Affairs Veeva Quality Assurance Specialist to… more
- Beth Israel Lahey Health (Boston, MA)
- …Word, Excel, PowerPoint or Access. **Preferred Qualifications:** + 1-3 years of clinical trial regulatory affairs experience preferred. **Competencies:** ... a difference in people's lives.** The Regulatory Specialist supports regulatory compliance for clinical...local bio safety committees on oncology human gene transfer trials . + Act as a liaison between the IRB… more
