Senior Biostatistician

Applicants must have the legal right to work in the country they are located at the time of application. Please note that we are unable to provide visa sponsorship for this role.

Contract initially for 6 months with opportunity to extend.

Preferred locations: UK, EU, SA.

The Senior Biostatistician will be responsible for performing, and validating statistical analyses in support of Medical Affairs, inclusive of overseeing the work of programming for external vendors in accordance with departmental SOP and guidelines, as needed.

About the Role Essential Functions

5+ years of experience working in clinical trials 2+ years Oncology TA experience required, recent experience strongly preferred Experience in CDISC Experience in SAP development and review, eCRF review Experience as study lead statistician Experience working on integrated/pooled analyses (e.g. ISS/ISE) Strong communication and collaboration skills

Qualifications

Master’s degree with >2 years of experience; OR PhD in statistics, mathematics or a related discipline with a statistical focus.

Required Skills

Proficient in drug development regulations pertinent to statistical analysis in the Oncology therapeutic space Proficient SAS programming skills Understanding of CDISC SDTM and ADAM models and standards is preferred Excellent writing and communication skills, demonstrated leadership abilities and excellent interpersonal skills. Able to work in a fast-paced, flexible, team-oriented environment.