Job Summary
Due to continuous business growth, we are expanding our Biostatistics team, and looking for a full-time Biostatistician to join our office-based team in Central London or Stirling. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success.
This role is responsible for Biostatistics activities for clinical trial projects; to ensure that work is completed within the defined time frames to appropriate quality levels, and present the Biostatistics function at conferences, external non-study meetings and bid defense meetings. If you want an exciting career where you can use your previous expertise and develop and grow your career even further, then this is the opportunity for you.
Responsibilities
* Contribute to clinical development of plan preparation;
* Review of study protocol and preparation of statistical methodologies;
* Development of detailed Data Analysis Plan for assigned projects;
* Programming of study analysis, review of study results and preparation of statistical methods section for clinical/statistical reports;
* Communicate project requirements for CRF design, database design and database clean-up to ensure the key study variables are suitable for analysis;
* Communicate statistical results to medical writing personnel to ensure accurate interpretation.
Qualifications
* Ph.D. degree in Biostatistics / Statistics / Medical Statistics;
* Experience in SAS Programming;
* Knowledge of advanced statistical methods and knowledge of the pharmaceutical industry;
* Knowledge of regulatory requirements/guidelines for drug development;
* Previous experience in a pharmaceutical or CRO preferred.
#J-18808-Ljbffr