Description
We are looking for a
Study Data Manager (m/f)
Reference: -en
Start: asap
Duration: 12 MM++
Place: in Basel region
Branch: Herstellung von pharmazeutischen Spezialitäten und sonstigen pharmazeutischen Erzeugnissen
Your tasks:
- 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
Your qualifications
- 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
Skills:
- Clinical data manager