Associate Director, Statistical Programming €55,000 - €70,000
- Clinical Research, Clinical Administrator, Clinical Project Manager, Clinical Research Associate, Clinical Research Nurse, Clinical Services, Clinical Supplies, Clinical Trials Manager / Administrator, Drug Safety, Feasibility, Pharmacoeconomics, Pharmacovigilance, Study Site Coordinator, Study Start Up, Data Management / Statistics, Clinical Data Management, Informatics, SAS Programming, Statistics, Information Technology, Design, Information Services, Programming, Medical Affairs, Medical Advisor, Project Management, R & D Project Management, Quality, QA / QC, Quality Validation Engineer, R & D , Biochemistry, Biology, Biotechnology, Chemistry, Pharmacology, Pre - clinical, Scientific, Regulatory Affairs, Sales / Commercial, Sales
We are looking to retain an Associate Director, Statistical Programming to be office based in Europe.
What are your responsibilities?
- You will oversee the delivery of studies across multiple therapeutic areas. You will play a key role in developing the programming team, interact closely with key stakeholders and vendors, developing tools and processes to deliver the portfolio of studies.
- Recruitment of both contract and permanent Staff.
- Identify opportunities to improve quality, efficiency, and effectiveness; and provide practical solutions for problems.
- Lead the provision of technical consulting expertise to the specification and delivery of the SDTM, RDB databases; TFL outputs; and CRT packages.
What will an ideal candidate look like?
- BSc or MSC in Mathematics or Statistics
- Extensive /Advance level of SAS programming experience
- Line management experience
- Knowledge of CDASH/SDTM/ADaM CDISC
- Clinical trial experience
Do you think this is for you?
Do you maintain some or many of these traits?
Apply for the chance to be apart of the process
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