Statistician - SM/AD

PURPOSE OF THE JOB :

The position is responsible for Developing, coordinating, and provides biostatistical support at trial level.

CORE JOB TASK

• Develops individual protocols and data analysis plans and determines appropriate statistical methodology for data analysis.

• Participates in database design meetings to ensure that the data evaluated are in high quality and satisfy analysis requirements.

• Collaborates with the statistical programming staff to ensure that all programs meet analysis requirements, internal standard operating procedures, and external regulatory requirements.

• Analyzes data and interprets results from clinical trials to meet objectives of the study protocol. Applies and implements basic and complex techniques to these analyses under supervision.

• Prepares oral and written reports to effectively communicate results of clinical trials to the project team.

• Provides responses to queries relating to study design, analysis, and interpretation posed by the clinical monitors, regulatory agencies, and/or investigators.

• Participates with management in discussions with corresponding scientific personnel at regulatory agencies and with investigators concerning proposed or ongoing studies.

• Involved in research activities for innovative statistical methods and applications in clinical trial development

MINIMUM REQUIREMENTS

• Master's degree in Statistics, Biostatistics, Mathematics, or a related field. A PhD degree is a plus;

• A minimum of 68 years’ experience in statistical experimental design and analysis, preferably in a pharmaceutical or biotech setting;

• Proficiency in statistical programming languages, such as R or SAS;

• Knowledge of machine learning and data mining techniques;

• Excellent problem-solving skills and the ability to work both independently and collaboratively;

• Strong written and verbal communication skills, with the ability to explain complex statistical concepts to non-statisticians;

• Fluent in English.