We are an Award Winning CRO specialising in data focussed projects supporting clinical human trials across Europe. Developing life saving drugs supporting global pharma, biotech, medical devices and animal health partners with ground-breaking clinical develop services. Ideally you would have experience in a CRO or Pharma background, leading studies and for the right candidate my client would be willing to pay a very competitive rate.
• Acting as Lead Programmer across multiple studies.
• Creator of CDISC compliant SDTM and ADaM programs and supporting documentation.
• Senior role will include project leadership activities.
• Minimum of 4+ years SAS Programming experience.
• Expertise in CDISC standards, including thorough understanding of SDTM / ADaM.
• Experience of leading project teams.
• Understanding of clinical development process.
• Leadership and mentoring skills.
email@example.com / 0203 019 5963