Principal Statistician

Location: Via Milano

Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do.

A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description You will contribute to statistical activities related to global clinical trials and work closely with international teams of statisticians, programmers and data managers, including the role of biostatistics project  this role, you will:

Act as a communication line for project teams, clients, vendors and internal team on statistical questions

Conduct statistical analysis for clinical trials including, interim analysis, final analysis, analysis for DSMBs/DMCs and PK analysis

Develop and review study protocols, statistical analysis plans, analysis dataset specifications according to CDISC ADaM standard and other project-specific documents

Review statistical deliverables such as tables, figures, listings and analysis datasets

Conduct departmental induction course and project-specific training for statisticians and SAS programmers

Prepare for and attend internal and external study audits pertinent to Statistics Participate in preparation of internal/external audits follow up Provide input to standard operating procedures and other Quality Systems Documents (QSDs) pertinent to activities of Biostatistics department

Liaise with DM on statistical questions related to data issues

Participate in bid defense and in kick-off meetings

Lead teams of SAS programmers and/or statisticians on the project level

Qualifications

MSc in Statistics or equivalent

Full working proficiency in English Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research

Expert knowledge and understanding of the SAS programming

Expert knowledge and understanding of CDISC ADaM standard

Expert knowledge and understanding of adaptive designs

Expert knowledge and understanding of sample size calculation

Expert knowledge and understanding of relevant regulations and guidelines (e.g. FDA, EMA, ICH)
Ability to apply advanced statistical techniques in support of clinical research studies and to analyze, interpret, and draw conclusions from complex statistical information

Ability to consult with clinical investigators, interpret research requirements, and determine statistical analysis strategies

Strong presentation and communication skills

Please submit your CV in English.

Additional Information Our mission is to be the best CRO in the world as measured by our employees, clients, sites, and vendors.

Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way.
#J-18808-Ljbffr