**Biostatistician required for a full-service clinical contract research organisation (CRO) based in London **
You will be responsible for leading the Biostatistics activities for multiple complex clinical trial projects, working directly with the client and collaborating with other departments and Clinical Trial Management team, operating in a leadership position and representing the Biostatistics department at client meetings.
You will be responsible for the development of analysis databases and detailed Data Analysis Plan for assigned projects. Collaborating with the wider statistics team further responsibilities will include programming of study analysis, review of study results, and preparation of statistical methods section for clinical/statistical reports, and related regulatory submission documents. You will communicate statistical results to medical writing personnel to ensure accurate interpretation; and collaborate with Global Statistics team members and programmers to ensure study outputs are produced to a high quality and in a timely fashion.
You will have a MSc or PhD in biostatistics, or equivalent areas and strong relevant industry experience with expertise in biostatistical methodologies applicable to Clinical Trials. Strong SAS Programming experience is also desirable along with excellent communication and leadership skills
- Agency: Cpl Life Sciences
- Contact: Stephen Wincott
- Reference: JO-2102-462470
Website: Cpl Life Sciences
- Posted: 9th February 2021
- Expires: 9th March 2021