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:
1. Act as a communication line for project teams, clients, vendors and internal team on statistical questions
2. Conduct statistical analysis for clinical trials including, interim analysis, final analysis, analysis for DSMBs/DMCs and PK analysis
3. Develop and review study protocols, statistical analysis plans, analysis dataset specifications according to CDISC ADaM standard and other project-specific documents
4. Review statistical deliverables such as tables, figures, listings and analysis datasets
5. Conduct departmental induction course and project-specific training for statisticians and SAS programmers
6. Prepare for and attend internal and external study audits pertinent to Statistics
7. Participate in preparation of internal/external audits follow up
8. Provide input to standard operating procedures and other Quality Systems Documents (QSDs) pertinent to activities of Biostatistics department
9. Liaise with DM on statistical questions related to data issues
10. Participate in bid defense and in kick-off meetings
11. Lead teams of SAS programmers and/or statisticians on the project level
Qualifications
12. MSc in Statistics or equivalent
13. Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research
14. Expert knowledge and understanding of the SAS programming
15. Expert knowledge and understanding of CDISC ADaM standard
16. Expert knowledge and understanding of adaptive designs
17. Expert knowledge and understanding of sample size calculation
18. Expert knowledge and understanding of relevant regulations and guidelines (e.g. FDA, EMA, ICH)
19. Ability to apply advanced statistical techniques in support of clinical research studies and to analyze, interpret, and draw conclusions from complex statistical information
20. Ability to consult with clinical investigators, interpret research requirements, and determine statistical analysis strategies
21. 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.