, 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...
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...
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...
Abbottinternal stakeholders Collaborates and interact with QA, Global Monitoring, clinical Study Start-Up teams, Global Clinical... are reached and potential country issues properly followed-up. Collaborate and liaise with Clinical Study Teams and Global...
ICONquery 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...
Lifelancer