Principal Statistician (Pharmacokinetics)

Psi CRO Ag; France; Sur place; EUR 50 000 - 70 000; Plein temps

Résumé du poste

Psi CRO Ag is seeking a Biostatistics Project Lead in France to contribute to statistical activities in global clinical trials. The role involves leading teams of statisticians and programmers, conducting various statistical analyses, and preparing protocols according to CDISC ADaM standards. Successful candidates will have an MSc in Statistics, expert knowledge in SAS and pharmacokinetics principles, along with strong communication skills. This is a full-time position requiring fluency in English.

Qualifications

• Full working proficiency in English.
• Expert knowledge of statistical principles used in clinical research.
• Experience in conduct of NCL and population PK analysis.

Responsabilités

• Act as a communication line for project teams regarding statistical questions.
• Conduct statistical analysis for clinical trials.
• Lead teams of SAS programmers on the project level.

Connaissances

Statistical analysis

SAS programming

Communication skills

Statistical principles and methods

Formation

MSc in Statistics or equivalent

Outils

Phoenix WinNonlin

NLME

Description du poste

Full-time

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 lead.

In 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
• 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 pharmacokinetics principles, concepts, methods and standards used in clinical research, including the conduct NCL and population PK analysis
• Expert knowledge and understanding of Phoenix WinNonlin and NLME
• Expert knowledge and understanding of relevant regulations and guidelines (e.g. FDA, EMA, ICH)
• Ability to apply a range of 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.