Clinicaltrials Gov Jobs (NOW HIRING)

Maintain and update clinicaltrials.gov, collaborate with biostatisticians to create statistical analysis plans; clean study data and create plans for data cleaning; analyze study data * Create data ...

Manages clinical trial compliance and reporting on ClinicalTrials.gov; supports data sharing, export control, and controlled research activities. * Serves as the university's liaison with external ...

... clinicaltrials.gov, including facilitation of Quality Assurance (QA) * Participate in the collection of data, supporting both human and animal protocols. * Provide education and training to ...

Familiarity with NCCN guidelines and ClinicalTrials.gov * Ability to work independently in a hybrid environment; must be Dallas area based Strong Candidates Will: * Demonstrate strong clinical ...

Maintain protocol development databases, ClinicalTrials.gov records, and internal tracking systems. * Plan and facilitate monthly disease committee teleconferences, prepare meeting agendas, generate ...

For example, NCBI develops and delivers PubMed, an index of over 29 million biomedical research abstracts; and maintains ClinicalTrials.gov, a database of over 400,000 clinical studies around the ...

... clinicaltrials.gov, including facilitation of Quality Assurance (QA) * Participate in the collection of data, supporting both human and animal protocols. * Provide education and training to ...

Help maintain timely and accurate study registration and updates on ClinicalTrials.gov and other applicable registries. Coordinate Clinical Trial Team meetings and drive action item follow-up. ...

Maintain all clinical trials information on clinicaltrials.gov. Additional related duties as assigned-5%. * Manage correspondence, generate materials, and execute administrative tasks for ...

For example, NCBI develops and delivers PubMed, an index of over 29 million biomedical research abstracts; and maintains ClinicalTrials.gov, a database of over 400,000 clinical studies around the ...

Prepare and submit Initial IRB submissions, amendments, continuing reviews, and reportable events to the IRB while serving liaison with the JHU IRB, ClinicalTrials.gov, and external sponsors.

... ClinicalTrials.gov and other applicable registries. ● Coordinate Clinical Trial Team meetings and drive action item follow-up. ● Maintain clinical operations trackers, databases, and document ...

Ensure timely archiving of biologic specimens and clinical trial data and support registration and maintenance of studies on ClinicalTrials.gov. * Review Data and Safety Monitoring Plans (DSMPs) and ...

... ClinicalTrials.gov registration and results reporting, aligning IRB determinations with federal and sponsor requirements. Education, Collaboration, and Special Projects • Develops, delivers, or ...

Prepare and submit Initial IRB submissions, amendments, continuing reviews, and reportable events to the IRB while serving liaison with the JHU IRB, ClinicalTrials.gov, and external sponsors.

Regulatory & Compliance Support Maintain study registrations and results reporting in ClinicalTrials.gov and applicable international registries. Support regulatory submissions, amendments, and ...

Integrate diverse data sources-KOL & investigator interviews, conference intelligence, clinical-trial/market databases (e.g., clinicaltrials.gov, TrialTrove, BioMedTracker, Evaluate, Cortellis ...

Stay current with and manage regulatory processes including IRB, FDA, NIH, HIPAA, CITI, clinicaltrials.gov, Florence portal. * Responsible for training and supervising research trainees, students and ...

Assists in the maintenance of clinicaltrials.gov information for Investigator Initiated Trials and Sponsored Research Agreements. * Promotes research revenue cycle best practices through the ...

Maintain all clinical trials information on clinicaltrials.gov. Additional related duties as assigned-5%. * Manage correspondence, generate materials, and execute administrative tasks for ...