, as required, CRAs are accountable for study start-up and regulatory maintenance. Tasks may include collection, preparation, review... Authorities for start-up and for the duration of the study. Contributing to the nomination and selection of potential...
Syneos Health, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase... visit reports, generating follow-up letters and other required study documentation Collaborate and liaise with study team...
IQVIA, site selection and study start-up; and May be responsible for other projects and responsibilities as assigned...-award study feasibilities, build and maintain strategic relationships with our network of sites, and develop key strategies...
Medpacequery generation and resolution. May support start-up phase Ensure copies/originals (as required) site documents... findings and action plans by submitting regular visit reports, generating follow-up letters and other required study...
IQVIAquery generation and resolution. May support start-up phase Ensure copies/originals (as required) site documents... findings and action plans by submitting regular visit reports, generating follow-up letters and other required study...
IQVIA, etc.). REQUIRED KNOWLEDGE Local knowledge / expertise of regulatory environment, study start up process and associated timelines...) Contribute to, deliver and/or lead CRA, Investigator and Study Coordinator training Oversight and monitoring of applicable...
IQVIA, and study start up. You should be excited about working in a fast-paced environment within a hard-working and welcoming team..., and join our Clinical Affairs function as a Clinical Research Associate or Senior Clinical Research Associate (CRA). The role of CRA...
Abbott