- Bausch + Lomb (Juneau, AK)
- …clinical , labeling, adpromo areas. Serve as a strategic advisor to project teams, ensuring regulatory compliance, influencing key stakeholders, and optimizing ... business outcomes. **Responsibilities:** + Formulate, lead, and drive integrated regulatory strategies across CMC and clinical /non- clinical , labeling,… more
- Sanofi Group (Morristown, NJ)
- …+ External contacts: Investigators, Clinical Site Services Providers, early phase Clinical Research Organizations, clinical trial vendors, clinical ... possible. Ready to get started? **Main Responsibilities** **At the project level, the Clinical Lead, ECET will...Investigators, Clinical Site Services Providers, early phase Clinical Research Organizations, clinical trial… more
- Cedars-Sinai (Beverly Hills, CA)
- … clinical study coordination, subject recruitment/enrollment, data management/integrity, regulatory compliance, project /study evaluation and interfacing with ... department process (grade, attribution, treatment, etc.), and reports to regulatory and sponsor as required. + Records research...care that allows for safe and effective collection of clinical research data. + Triages patient by… more
- Cedars-Sinai (Los Angeles, CA)
- … clinical study coordination, subject enrollment, data management/integrity, regulatory compliance, project /study evaluation and interfacing with participants ... we'd love for you to apply. We highly value ** clinical research nurse experience** , as you'll...department process (grade, attribution, treatment, etc.), and reports to regulatory and sponsor as required. + Records research… more
- Ohio University (Athens, OH)
- …the biomedical research process while ensuring the integrity and quality of clinical research is maintained and conducted at the Heritage College Clinical ... tasks or assist with medical procedures performed in the clinical research setting, including but not limited...the research protocol + May assist with research project budget development + Ensuring site… more
- Boehringer Ingelheim (Ridgefield, CT)
- …Global Regulatory Strategy Document. + In cooperation with US/Global Labeling, provide project -related US regulatory input into content of the draft CCDS. + ... US Food and Drug Administration. + Provide analysis, advice and guidance on US regulatory strategies. + Research information on regulatory standards and… more
- University of Utah (Salt Lake City, UT)
- …and draft study protocol amendments. + Oversees, coordinates, and conducts monitoring of clinical research studies as needed. + Acquire and abstract primary or ... based on findings + Create, or manage creation of, any type of clinical research reporting document such as manuscripts, posters or oral presentations… more
- Parsons Corporation (San Antonio, TX)
- …responsible for assisting with the collection of supporting documentation, coordinating clinical research studies, and maintaining regulatory requirements. ... IACUC/IRB requirements. + Develop and coordinate the implementation of clinical research studies, including regulatory requirements, maintenance… more
- University of Colorado (Aurora, CO)
- …recruit a doctoral-level, quantitatively-oriented, highly-motivated researcher to contribute to clinical and epidemiologic research focused on injury prevention ... including dozens of published peer-reviewed manuscripts and scientific presentations. Our research also deliberately seeks to fill clinical and scientific… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …and functions include clinically facing clinical research management; regulatory affairs; training and education; and project management and monitoring ... across core CTO functions targeting non-faculty members of the study team: clinical research coordinators, regulatory operations, and research… more