towards development of clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual, investigator... of Investigator agreements and trial payments; Is responsible for clinical data review to prepare data for statistical analyses...
educational materials and support programs for personnel. Discuss Investigator Initiated and Collaborative study concepts...
investigator/lead, generating original technical ideas and research or development strategies. Represents TMS in cross functional...
of scientific protocols, Investigator Brochures, Clinical Study Reports, Clinician Reported Outcome Dossiers, regulatory submissions...
development. Contributes to design, analysis, interpretation, presentation and reporting of scientific protocols, Investigator...
of scientific protocols, Investigator Brochures, Clinical Study Reports, Clinician Reported Outcome Dossiers, regulatory submissions...
development. Contributes to design, analysis, interpretation, presentation and reporting of scientific protocols, Investigator...
investigator/lead, generating original technical ideas and research or development strategies. Represents TMS in cross functional...
closely with the principal investigator to: Assist with running pipelines on a Unix-based high performance compute cluster...
, you will: Collaborate with the investigator to ascertain study patient eligibility for clinical trial, including documentation of criteria...
, monitoring plan, study manual, investigator brochure, annual reports) with minimal direction. Ensure trial registration... and execution of Investigator agreements and trial payments. Leads clinical data review to prepare data for statistical analyses...
approaches used. Effectively work and communicate with investigator, staff and patients in professional, sensitive and mature...
, and principal investigator meetings Develop and communicate APTURE’s value proposition in a continuously evolving space...
presentation and peer-reviewed publications Managing nonregulated studies (e.g., Investigator initiated, Registries, Real-world...
towards development and approval of clinical trial protocols, informed consents, investigator brochures, committee charters...
consents, investigator brochures, committee charters, and other study materials. Conduct routine review of adverse events (AEs...
for company sponsored and investigator initiated research. Collaborate with evidence generation colleagues from Preclinical... execution (investigator brochures, training materials, etc.) Work closely with Medical Safety team to ensure adverse events...
for company sponsored and investigator initiated research. Collaborate with evidence generation colleagues from Preclinical... execution (investigator brochures, training materials, etc.) Work closely with Medical Safety team to ensure adverse events...
towards development of clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual, investigator... of Investigator agreements and trial payments Responsible for clinical data review to prepare data for statistical analyses...
trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual... and oversees Clinical Research Associates (CRAs); Oversees and supports the development and execution of Investigator agreements...