Job Title: Clinical Study Data Lead Duration: Full Time Location: Cincinnati, OH Technical/Functional Skills:
Overall in-charge of all Data Management activities for a study/ies including Study Set up, Conduct and Close Out.
Primary point of contact for CDM and works are liaison for CP, DAS and CCS activities too
Monitors and evaluates overall study progress, identify the potential risk / challenges faced during the course of the study
Conducts regular team meetings for study updates and provides guidance on study related issues to Roche as well TCS internal teams
Monitor, maintain & report KPI / SLAs /metrics on the study
Performs tasks/activities as communicated by the TCS Group Leader (GL) and / or Project Manager (PM) and Roche Study Data Manager (SDM)
Ensures adequate resource for the Study throughout its lifecycle in collaboration with Group leader and informs Roche (SDM and/or Alliance Manager (AM) as applicable) contact of any changes in staff
Keeps TCS Group Lead & Project Manager fully informed about the need for the resources so the resource requests can be finalized with Roche AM and TCS PM
Keeps record of all activities to ensure the smooth flow of the study throughout its lifecycle
Set priorities and targets of the study within the CP, DM, CCS, DAS teams
Responsible for recruitment, selection, training of team members & managing attrition
Works as mentor for DM staff assigned on the study/ies
Preferred Educational Qualification for the role: Bachelors/Masters Degree in Life Sciences with overall 6 to 8 years of relevant experience Preferred experience for the role:At least 6 + years of related work experience in a clinical or pharmaceutical industry/company
