Senior Statistician

PSI CRO

$110K — $130K *
US-AnywhereRemote in Durham, NC
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • MSc in Statistics or equivalent
  • Expert knowledge of statistical methods in clinical research
  • Proficiency in SAS programming
  • Familiarity with CDISC ADaM standards
  • Experience with adaptive study designs
  • Ability to perform sample size calculations
  • Understanding of FDA, EMA, and ICH regulations
  • Strong analytical and interpretative skills in statistics
  • Effective communication and presentation abilities

Responsibilities

  • Serve as the communication hub for teams, clients, and vendors regarding statistical inquiries
  • Conduct statistical analyses for clinical trials, including interim and final analyses
  • Prepare and review study protocols and statistical analysis plans
  • Evaluate statistical outputs such as tables and figures for accuracy
  • Lead departmental training for staff on statistical principles and programming
  • Prepare for and participate in audits related to statistics
  • Contribute to the development of standard operating procedures

Benefits

  • Supportive and straightforward recruitment process
  • Opportunity to work with global teams on impactful clinical trials
  • Training and development opportunities for career growth
  • Collaborative work environment among cross-functional teams
  • Engagement in high-level statistical discussions and strategic decision-making
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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