Study Data Manger (m/f)

-Lead the CDM study team and maintain oversight of all activities for one or more studies
-Escalate study issues appropriately and address corrective action plans
-Responsible for the implementation of standards within PDM across one or more CDM study teams
-If necessary, perform program-level activities for molecules where a Program Data Leader is not assigned
-Responsible for complex deliverable for the subfunction for one or more studies
-Effectively communicate ideas, project goals and status of work and independently present at department meetings
-Set targeted timeframes for deliverables and anticipate potential scenarios that may create timeline delays
-Evaluate probability, impact and priorities of risks and develop and implement mitigation plan
-BA/BS degree or equivalent and moderate industry-related experience
-Moderate practical and theoretical expertise within your subfunction
-In-depth understanding of the business
-Ability to work under minimal guidance
-Functional knowledge in the development of processes, training and related documents
-Technical proficiency and ability to complex assignments within defined parameters
-Ability to partner with PTM training community to ensure best training practices are being leveraged in focused training
-Experience with RAVE is of advantage

Weitere Qualifikationen: Clinical data manager