Opening for experienced CRA to work for Remote CRA/ Central CRA, @ RPS /PRA/@ Novartis/ Hyderabad @ D6

Role: Central Clinical Research Associate


Job Description:

Perform ongoing central remote monitoring of patient data using available online data sources (eCRF, IRT, central lab etc.) to ensure consistency and correctness of the data ,Communicate any observations; deviations to protocol, safety alerts, quality issues, entry patterns, risk factors etc. that may affect the planned conduct of the trial to the clinical team and local ICRO organization / directly to site for timely follow-up actions and issue resolution. Perform data query resolution process (with site, local ICRO CRA and DM ) As required update ClinAdmin or other study management systems with e.g. key trial country and site event dates and enrollment figures. Provide input to the Monitoring Plan, eCRF design & review, and other documents and systems as applicable, ensuring accurate format for central monitoring. Acts as a close partner with the local ICRO CRAs, CSMs and Global Trial Lead. A team member of the clinical trial team (CTT) Interact with DM / CAF/ programming group and/or other line functions to ensure that efficient tracking and data reports are generated as required with flags and alerts for relevant deviations. 


Education:

UG - Any Graduate - Any Specialization, Graduation Not Required
PG - Any Postgraduate - Any Specialization, Post Graduation Not Required
Doctorate - Any Doctorate - Any Specialization, Doctorate Not Required

Contact @: Mr. Sai Kumar

e mail id: skumar2@rpsweb.com