KOFFI ENAM ADANLESSOSSI
Silver Spring,VA
Summary
Detail-oriented, organized, and competent Statistical SAS Programmer with experience working in the pharmaceutical industry and providing knowledge in data modeling, SAS data analytics, data extraction, transformation, analysis, quality assurance, and business analysis within the healthcare industry.. Adept in operating SAS 9.4, maintaining updated databases, extraction of usable data from information as well as writing required syntax. Passionate about achieving efficient processes with specialized data extraction, transformation, and analysis within the healthcare industry.
Overview
5
5
years of professional experience
1
1
Certification
Work History
Federal Advisory Partners (Now TRIA)
Arlington, VA
10.2022 - Current
- U.S. Department of Veterans Affairs (VA), Veterans Health Administration (VHA), Office of Finance (OF), Forecasting and OF leadership engaged F|A|P to develop an econometric model that support OF's efforts in formulating and negotiating the M
Clinical SAS analyst
PRA Health Sciences
01.2022 - 09.2022
- Analyzed data using SAS Procedures such as Proc Means, Proc Tabulate, Proc Freq, Proc Summary.
- Prepared new datasets from raw data files using Import Techniques and modified existing datasets using Data Steps, Set, Me
- Generated customized reports using the DATA _NULL_ and PROC REPORT techniques.
- Created reports using PROC REPORT and used ODS statements to generate reports in HTML, PDF, RTF, and list formats.
- Generated high quality reports and presentations into different formats, such as HTML, RTF, and PDF through employing S
- Extensively Used SAS/ODS for generating different output formats as requested.
- Involved in designing, implementation, and validation of SAS programs to produce descriptive/categorical statistical an
- Developed SAS code to automate transfer of results from PROC FREQ procedure output to Excel spreadsheets utilizing SAS
- Used PROC SQL procedure, connected to different databases via pass through facility to execute SQL queries using the da
- Established domain models according to SDTM specs and created new domains that are CDISC compliant and implemented the
- Developed SAS programs for listings and tables for data review and presentation, including Case Report Tabulations as p
- Mapped clinical trial data according to SDTM Model provided by the CDISC standards and expert in understanding SDTM mo
- Generated ADaM specifications under the guidance of project statistician.
- Involved creating ADaM datasets and generated TLF (Table, Listing, Figure).
- Assisted to create SAS datasets for in-house post-hoc statistical analysis and used SAS data steps for large data processing f
- Worked under the supervision of senior SAS developers to manage large volume of structured and unstructured data as well
- Helped end-users with software functionality by explaining techniques to deploy content to SAS web-based tools for distri
- Provided reports related to data management, descriptive tables, and gave data displays on the screen as and when required.
- Conducted post-hoc or exploratory statistical analysis with team and under the guidance of project statistician.
- Knowledge of the FDA Guidance, Regulatory Compliance, and Good Clinical Practices (GCP).
- Reviewed client requirements to understand projects related to clinical study report for agreement between in-text tables and
Clinical SAS programmer
Emmes
11.2020 - 11.2021
- Created and executed SAS edit check programs and SAS macro and format libraries.
- Communicated information about creating CDISC-compliant datasets.
- Prepared documentation with all datasets and variables within, including derived variables, and the project as whole.
- Performed data checks as needed, to ensure integrity and correctness of data displays.
- Prepared documentation for programs.
- Programmed customized data displays, including data listings, summary tables, and routine graphics in accordance with app
- Wrote codes with Base SAS programs, SAS procedures, or standardized macros.
- Performed data checks as needed to understand structure and content of data.
- Involved in statistical programming and validation of Analysis Datasets and Tables, Listings, Graphs (TLF’s).
- Created SDTM datasets for patient narratives.
- Created Patient narratives and generated XML outputs for FDA regulatory submissions.
- Assisted in preparation of various study specific documents.
- Assisted programming for ISS (Integrated Summary of Safety) tables and listings.
- Involved in data cleaning and edit checks.
Education
MS - Healthcare Administration
BS - Biological Sciences
Minor - Information System
Skills
- Microsoft Office Suites
- Communication skills
- Data analysis
- Problem-solving skills
- Statistical reports
- Econometric Forecasting
- Clinical trial understanding
- Analytical skills
- Detail oriented
- SAS programmer
- VHA Revenue Cycle
Certification
SAS Certified Programmer
Timeline
Federal Advisory Partners (Now TRIA)
10.2022 - Current
Clinical SAS analyst
PRA Health Sciences
01.2022 - 09.2022
Clinical SAS programmer
Emmes
11.2020 - 11.2021