Mark Senior
London
Summary
Organised and dependable biostatistician with 11+ years of experience in the industry. Successful at managing projects and always done with a positive attitude. Willing to take on greater responsibilities to meet team goals.
Overview
13
13
years of professional experience
7
7
years of post-secondary education
1
1
Certification
Work history
Senior Biostatistician
Fortrea/Labcorp/Covance
Maidenhead, Windsor and Maidenhead
2021.10 - Current
- Perform Lead Biostatistician role, providing statistical oversight and attending relevant project meetings.
- Perform project management activities for identified projects including resource planning, timelines and milestone management.
- Preparation of Statistical Analysis Plans (including mock TFL shells)
- Perform statistical analyses, quality check statistical analyses developed by other statisticians.
- Conduct overall statistical review of TFLs prior to client delivery.
- Develop statistical sections of protocols.
- Provide statistical input and review of CSRs.
- Preparation and review of randomization specifications and generation of randomization schedules.
- Developing company standard SAS macros for statistical modelling.
- Mentoring junior statisticians
Biostatistician II
Fortrea/Labcorp/Covance
Maidenhead, Windsor and Maidenhead
2019.05 - 2021.10
- Executed Lead Biostatistician responsibilities with statistical oversight across projects.
- Attended project meetings to ensure alignment with objectives and timelines.
- Prepared Statistical Analysis Plans and mock TFL shells for medium complexity studies.
- Conducted statistical analyses for medium complexity studies, ensuring accuracy and compliance.
- Reviewed TFLs comprehensively prior to client delivery for medium complexity studies.
- Provided statistical input and reviewed Clinical Study Reports for simple studies.
- Performed SAS programming to facilitate presentation and analysis of clinical trial data.
- Communicated project budget status and task progress effectively to line management and project manager.
Biostatistician I
Fortrea/Labcorp/Covance
Maidenhead, Windsor and Maidenhead
2018.03 - 2019.04
- Preparation of Statistical Analysis Plans
- Perform QC/statistical review of data displays for study endpoints.
- Statistical analysis of clinical trial data using basic methodology.
- Preparation of sections of statistical reports, as well as input into Clinical Study Report
- Perform sample size calculations.
- Generate randomization schedules from provided specifications.
- SAS programming and related activities for presentations and analyses of clinical trial data.
Statistical Programmer II
Fortrea/Labcorp/Covance
Maidenhead, Windsor and Maidenhead
2015.09 - 2018.02
- Develop and review SAS programs and outputs as required for the management of clinical trial data, tabulation of data, preparation of patient data listings, graphical output, creation of derived datasets and statistical analysis of data as specified in Statistical Analysis Plans.
- Interact with project team members in related disciplines e.g. Clinical Data Management, Clinical and Biostatistics.
- Assume team member responsibilities, including representing Statistical Programming at internal project team meetings and at client meetings.
- Assist with training, mentoring of Statistical Programming staff.
- Participate in Statistical Programming review of Case Report Forms, annotated CRFs, database structures and study related documentation.
Statistical Programmer I
Fortrea/Labcorp/Covance
Maidenhead, Windsor and Maidenhead
2014.08 - 2015.08
- Develop and review SAS programs and output as required for the management of clinical trial data, tabulation of data, preparation of patient data listings, graphical output, creation of derived datasets and statistical analysis of data as specified in Statistical Analysis Plans.
- Develop programs for ad hoc tables and listings. Write, modify, and maintain programs that produce diagnostics and listing for data review in support of Data Management.
- Carry out electronic data transfer (both incoming and outgoing).
- Set-up utilities/SAS based systems to assist and facilitate Clinical Data Management activities.
- Interact with project team members in related disciplines e.g. Clinical Data Management, Clinical and Biostatistics.
Placement Programmer
Fortrea/Labcorp/Covance
Maidenhead, Windsor and Maidenhead
2012.07 - 2013.08
- Develop and review SAS programs and output as required for the management of clinical trial data.
- Develop programs for ad hoc tables and listings. Write, modify and maintain programs that produce diagnostics and listings for data review in support of Data management.
- Display a positive attitude at all times, promoting and contributing to a good team spirit with a productive and professional environment.
- Develop good problem solving skills and a willingness to learn and seek advice from senior statistical programming staff.
Education
Master of Science - Medical Statistics
University of Leicester
Leicester 2016.09 - 2019.07
Bachelor of Science - Mathematics with Sandwich
University of Brighton
Brighton 2010.09 - 2014.07
Skills
- Organisation
- Communication
- Dedication
- Adaptable
Languages
English
Fluent
Certification
Chartered Statistician
Affiliations
- Outside of work, I’m passionate about health and music. I train five days a week and play basketball regularly to stay active. I’m also a self-taught keyboardist and dedicate time each week to playing and improving my musicianship.
Timeline
Senior Biostatistician
Fortrea/Labcorp/Covance
2021.10 - Current
Biostatistician II
Fortrea/Labcorp/Covance
2019.05 - 2021.10
Biostatistician I
Fortrea/Labcorp/Covance
2018.03 - 2019.04
Master of Science - Medical Statistics
University of Leicester
2016.09 - 2019.07
Statistical Programmer II
Fortrea/Labcorp/Covance
2015.09 - 2018.02
Statistical Programmer I
Fortrea/Labcorp/Covance
2014.08 - 2015.08
Placement Programmer
Fortrea/Labcorp/Covance
2012.07 - 2013.08
Bachelor of Science - Mathematics with Sandwich
University of Brighton
2010.09 - 2014.07