- GAP Solutions Inc (Bethesda, MD)
- …+ Maintains all professional certifications, if applicable. + Maintain a current clinical trial and clinical research study Good Clinical Practice GCP knowledge ... reports. + Enter data into research databases, systems and applications for ongoing studies . 4 + Verify study participants information and collect data and… more
- Boehringer Ingelheim (Ridgefield, CT)
- …+ Accountable for optimal planning, interpretation and data presentation of clinical studies from FIM throughout pivotal studies , ensuring integration of ... and other contributors), Clinical Development Plans or similar documents, Core Clinical Trial Protocols, including the CTP strategy and core CTP elements within a… more
- IQVIA (Durham, NC)
- **PURPOSE** IQVIA Design Analytics delivers clinical trial design optimization services that integrates drug development and clinical trial expertise with real ... world data, transformative technologies, methods, and work models. The Associate Design Analytics Director primarily supports client consulting engagements,… more
- Guidehouse (Bethesda, MD)
- …completeness of documents. + Assist researchers collect, organize, and maintain all study documentation to include investigator qualifications, trial logs, and ... regulatory related documentation description. + Collect, organize, and maintain all study documentation to include investigator qualifications, trial logs, and… more
- Merck (North Wales, PA)
- …Under the oversight of the System and Data Integration Lead (SDIL), the Associate SDIL is responsible for the integration between our source systems (primarily Data ... coordination between our company's IT and Supplier, across the studies assigned, for the integration of applicable systems data...the Supplier system) in order to support generation of study KRIs and Quality Tolerance Limits (QTL)s out of… more
- Pennsylvania State University (University Park, PA)
- …. JOB DESCRIPTION AND POSITION REQUIREMENTS: Part-Time Junior Policy Associate : Paid Internship to Implement a BIPOC Policy Scholars Program ... connecting legislative officials with those who specialize in data and scientific study relevant to policymakers' current policy agendas. This also provides a… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …areas centered around rare diseases and immune disorders. **Summary** The Associate Director, Quantitative Systems Pharmacology (QSP) will work within the ... include target prioritization, therapeutic modality selection, biomarker characterization and clinical trial design. In addition, he/she will develop a QSP strategy… more
- UCLA Health (Los Angeles, CA)
- …mobile scalp and intracranial EEG, electro-, and psychophysiological recordings on study participants; perform task presentation using virtual and augmented ... for research projects in a neuromodulation and neuroimaging laboratory; perform pre- study interviews of participants and families, consent of participants, and… more
- Bristol Myers Squibb (Princeton, NJ)
- …selection, chemical/biotherapeutic optimization, biomarker characterization, combination assessment, clinical trial design, and trial interpretation. Our ... project teams to design, execute and interpret preclinical and clinical studies + Independently collaborate with stakeholders to identify and interpret experiments… more
- US Army Corps of Engineers (San Francisco, CA)
- …as a GS-04, students must have completed two full academic years of post-high school study or have an associate 's degree. To qualify for a Pathways Internship as ... data. This position is eligible for telework, but is not a remote or virtual position. Applicants must be willing to report to the duty station location. Housing… more
- US Army Corps of Engineers (San Francisco, CA)
- …as a GS-04, students must have completed two full academic years of post-high school study or have an associate 's degree. To qualify for a Pathways Internship as ... as a student trainee to support scientists with projects and studies . Housing NOT provided, relocation incentive NOT provided. Responsibilities Assist experienced… more
- University of Utah (Salt Lake City, UT)
- …sponsors to communicate and resolve issues Assumes considerable leadership responsibilities of studies throughout the network Provides feedback on study site ... offers opportunities to work with high functioning, cutting-edge teams that study , understand and improve multi-site research. Bring your background in strong… more
- University of Colorado (Aurora, CO)
- …all the affiliated sites in the I-SCREEN Hub. + Direct activities related to study procedure and set up in accordance with NCI/CTEP requirements including but not ... with other I-SCREEN staff and investigators to facilitate I-SCREEN study start up and recruitment activities. + Participate in...participate in the annual CSRN in-person meetings and other virtual meetings as required. + Utilize resources in the… more
- University of Michigan (Ann Arbor, MI)
- …for a federally funded clinical trial . The study is a SMART trial lookin to evaluate three virtual treatment interventions for alcohol use disorder. As ... Considerations 3. Investigational Products Development and Regulation 4. Clinical Study Operations (GCPs) 5. Study and Site...prepared candidate for this role will have: + an Associate 's degree in Health Science or an equivalent combination… more
- Boehringer Ingelheim (Ridgefield, CT)
- …In alignment with Clinical Operations, interacting with current and potential BI study investigators to support clinical trial activities. + Facilitating ... logistical communications between BIPI and HCPs regarding Investigator Initiated Studies (IIS), External Collaborative Research, company study contracts, etc.,… more