Principal Statistician

PSI CRO

$100K — $130K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • MSc in Statistics or equivalent required
  • Expert knowledge of statistical principles and methods in clinical research
  • Proficiency in SAS programming
  • Familiarity with CDISC ADaM standards
  • Understanding of adaptive designs and sample size calculations
  • Knowledge of relevant regulations (FDA, EMA, ICH)
  • Ability to apply advanced statistical techniques and interpret complex data
  • Strong presentation and communication skills

Responsibilities

  • Serve as a communication link for project teams and stakeholders on statistical queries
  • Conduct comprehensive statistical analyses for clinical trials
  • Develop and review study protocols and statistical plans
  • Review statistical deliverables including tables and datasets
  • Conduct training for statisticians and SAS programmers
  • Prepare for and attend audits related to Statistics
  • Lead project teams of SAS programmers and/or statisticians

Benefits

  • Contribute to high-impact global clinical trials
  • Collaborate with international teams
  • Opportunities for professional development and training
  • Engagement in diverse statistical methodologies
  • Supportive recruitment process with guidance at every step
Full Job Description
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 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
  • 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


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.

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