Biostatistical Programmer Resume

Biostatistical Programmers work in research or pharmaceutical companies and develop SAS programs to analyze and report clinical data. They also develop and document datasets, tables, listings, analysis files or figures for clinical study or trials. If you are really interested to work in this profile, you will need a comprehensive and effective Biostatistical Programmer resume that will highlight your skills or credentials and will grab the attention of potential employers. Your resume must showcase expertise in SAS programming, SQL processes, clinical trials design and analysis principles, supporting clinical trials, developing tables and datasets as per specifications, troubleshooting programming issues, analysis of datasets in SAS, data and program quality control methods. To increase the chances of getting an interview call, include exceptional analytical, problem-solving, time-management, team-working and project management skills in your resume.

For more help, check out the given below sample Biostatistical Programmer resume and customize your resume accordingly:-

Biostatistical Programmer Resume Example

Sandra D. Ballard
4562 Green Avenue
New York, NY, 10002
Phone No: 212-774-7232
Email: sandraballard@anymail.com

Career Summary:

Highly-dedicated, enthusiastic, and professional Biostatistical Programmer with more than 5 years of experience in providing quality programming and analytical support for clinical study or trials. Expertise in designing and validating SAS programs, developing datasets, tables and figures for statistical analysis, troubleshooting statistical programming issues. Possess excellent programming, communication, team-working, project management, problem-solving and analytical skills along with the ability to maintain up-to-date knowledge of latest industry trends, advancements, programming and data standards.

Summary of Skills:

• Thorough knowledge of biostatistics, SAS and Matlab programming, clinical trial analysis, statistical data analysis plans and specifications, database management principles, clinical research regulations and requirements, data and software quality control, Windows and Linux operating systems
• Advanced SAS analysis and reporting skills along with the knowledge of SAS/BASE, SAS/MACRO, SAS/GRAPH programming tools as well as SDTM and ADAM datasets
• Proficiency in using MS SQL and relational databases as well as MS Office Suite applications
• Strong project management skills as well as the ability to solve complex programming issues
• Effective communication skills with the ability to present technical or project information to management personnel
• Ability to work in a fast-paced and challenging environment as well as under pressure
• Solid leadership skills as well as the ability to work in a team environment with clinical researchers, data managers, programmers and biostatisticians
• Strong organizational skills with the ability to work on multiple assignments simultaneously and complete work within specific deadlines

Work Experience:

Biostatistical Programmer
ASTEX Research Inc., New York, NY
September 2017 - Present

• Working collaboratively with technical team and developing SAS programs and standard software to generate datasets, listings, table shells, graphical representations or analysis files for clinical study or trial data
• Serving as the lead biostatistic programmer to provide technical support or training to less experienced programmers regarding data standards and programming as well as performing quality control of SAS programs, including source code, double-programming and log reviews
• Performing software testing and debugging functions and troubleshooting critical programming issues within the projects as well as developing SAS macros, templates, and other effective techniques for improving process efficiency
• Helping clinical teams in choosing appropriate analytical or statistical designs and data management approaches as well as writing study proposals including analysis sections to meet clinical study objectives
• Providing support in the implementation of computerized systems, subsystems or tools facilitating trial or project specific data analysis and documentation as well as suggesting effective solutions to biostatisticians regarding clinical trial database or other critical project issues
• Actively participating in the development and maintenance of specifications and related documentation for standard analysis datasets or files as well as reviewing and providing project deliverables as per client specifications

Biostatistical Programmer
Premier Corporation, New York, NY
April 2015 - August 2017

• Contributed in the overall development and management of new or junior biostatistical programming team as well as supported study team members, including project leads, statisticians and data managers in implementing statistical analysis plans for different clinical studies
• Provided support in programming and validating statistical analysis for clinical trials as per SAS data specifications as well as developed complete reports with accurate statistical results
• Reviewed project documentations for accuracy and completeness that included specifications, issue logs, deliverable status and statistical project plans as required
• Gathered and transformed clinical trial data into datasets for statistical analysis using SAS programming macro language as well as adhered to all department standards and regulatory requirements for programming, analysis and reporting of research projects or clinical trials
• Resolved unique queries related to data management and statistical analysis processes as well as performed quality control of data, SAS programs and related software to be used for analysis
• Contributing to the overall development and management of biostatistical projects as well as collaborated with management team to track project revenue, backlog, working days and times

Junior Biostatistical Programmer
Amgen Research Group, New York, NY
December 2013 - March 2015

• Assisted senior programmers in developing and implementing SAS programs and related software to provide trial or project specific listings, report-quality summary tables and graphical representations to the members of clinical team
• Maintained complete and accurate documentation of derived analytical data files for research team as well as assisted with data storage and management issues for new and ongoing projects
• Assisting lead programmers in identifying and developing effective solutions for critical programming issues within the projects as well as assessed and recommended new standards, policies and procedures as required
• Worked with biostatisticians and programmers to design and implement project analysis database structures as well as to program various algorithms for conversion between different database structures

Education:

• Bachelor's Degree in Computer Science
  Hofstra University, Hempstead, NY, USA
  2012

Certification:

• SAS (Statistical Analysis System) Certified Advanced Programmer
  2013

Reference:

On request.