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Sas Programmer Team Leader

Location:
Durham, NC
Posted:
February 21, 2025

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Resume:

DENNIS SMYTHE-MACAULAY

**** ********* ****** **.

Apt 1433

Durham, NC 27713.

919-***-****

Email: ********@*****.***

CLINICAL CERTIFIED SAS PROGRAMMER

Competent team leader and career oriented, professionally skilled and technically trained, possessing the ability

of multi-tasking and working until completion. Helpful, hardworking, honest, dedicated and self-motivated

individual with a drive for success while implementing a positive working environment. Accomplishment at

working with individuals and groups at various levels and completing team projects, while exercising

techniques in assigning and directing a successful team. Attention to detail, execution and quality of

performance. Understand the principles of effective time management and the necessity to work efficiently and

effectively day-to-day in a high speed, high-volume environment.

PROFESSIONAL EXPERIENCE

• In - depth familiarity in analyzing Clinical Trial Data, generate tables, listings and figures (TLF’s).

• Working knowledge of all Phases (I –IV) of Clinical Trials, using guidelines of Title 21 of the Code of

Federal Regulations in new drug development and application.

• Experience in creating, validating and maintaining CDISC, SDTM and ADaM datasets.

• Proficient in SAS Programming, merging SAS Data Sets, SAS Macro Facility.

• Experience in producing reports employing various SAS procedures like PROC SQL, PROC REPORT,

PROC FORMAT, PROC TABULATE, PROC FREQ, PROC MEANS, PROC GLM, PROC REG,

PROC UNIVARIATE and PROC SUMMARY.

• Thorough working understanding of SAS/BASE, SAS/SQL, SAS/ODS, SAS/STAT, SAS/GRAPH and

SAS/MACRO.

• Good analytical and communication skills, ability to work independently with minimal supervision and

also to perform as part of a team and willing to take on extra responsibility in getting the work done.

• Active and contributing member to South East SAS User Group.

CERTIFICATES & DEGREE:

• SAS Certified Clinical Trials Programmer Using SAS 9

• SAS Certified Advanced Programmer for SAS 9.

• SAS Certified BASE Programmer for SAS 9.

THE UNIVERSITY OF NORTH CAROLINA, Chapel Hill, NC

Bachelor of

Science in Mathematics, June 2008.

RELATED JMP COURSES:

Data Exploration

ANOVA and Regression

Introduction to Scripting Advance Scripting

Statistical Process Control Design of Classic

Experiment.

TECHNICAL

SKILLS:

Operating System: UNIX, Ubuntu, Linux, Windows 98/2000/NT/XP/Vista/Windows 7.

Languages: Pascal, FOTRAN, C++, Java and Matlab.

Office Tools: MS Office (Word, Excel, Access, PowerPoint and FrontPage)

Statistical Packages : SAS, SPSS, SAS/JMP, SUDAAN, STATA and SQL.

EMPLOYMENT

Senior Data Analyst

Key Responsibilities: o Review and provide/collect SAS feedback on data transfer specifications

and test transfers from external vendors as applicable for reconciliation

purpose, SDTM and other programming tasks.

o Review and provide/collect SAS feedback on eCRF development and

changes and evaluate the impact on programming activities and exports.

o File documentation associated with client delivery including project emails

on an ongoing basis and perform final archival activity at study close.

o Define specifications/test data to facilitate vendor and/or SAE reconciliation,

medical coding, investigator payments, data review (e.g., SAS data checks

and patient profiles) and other needs, as requested.

o Develop QC test plans, perform independent unit testing, complete

documentation for SAS code installs and utilize source code management

software.

o Set up default clinical data transfer and/or perform scheduled and ad-hoc transfers.

SAS Data Programmer

Key Responsibilities: o Draft, update and maintain the Master Plan for assigned project and review

study plans for other departments.

o Review and provide feedback on project timelines and ensure that project

tasks are completed timely and with acceptable quality.

o Assume responsibility for project budget, and perform monthly time

projections.

o Attend internal team meetings and relevant client team meetings, as

needed.

o Review data transfer specifications and test transfers from external vendors

as applicable for reconciliation purpose

o Review and provide/collect SAS feedback on eCRF development and data

structure changes and evaluate the impact on programming activities

o Define specifications/test data, program and generate reports to facilitate

vendor and/or SAE reconciliation, medical coding, investigator payments,

data review (e.g., SAS data checks and patient profiles) and other needs, as

requested

o Define specifications and test plans for data imports

o Develop specifications and programs to integrate local lab normal ranges

with data extract

o Set up project-specific J-Review system for InfoLink and/or InForm.

o Support programming activities for medical coding group, including

integration of coded terms with data extract files

o Develop QC test plans, perform independent unit testing, complete

documentation for SAS code installs and utilize source code management

software

o Assist with process improvement initiatives, as agreed to by management

HISTORY: CREE, Durham, NC

May, 2013 – Present.

Manufacturing Technician

• Maintains a Statistical Process Control System using SAS JMP software.

• Sets up reactor runs for daily production.

• Experience with RTA, probers, Wet Benches and Temescal evaporators.

• Calculates and interprets process capability indices.

• Creates OCAP steps for operators to take when out of control state occurs.

• Effectively work with Technicians/Engineers to resolve discrepancies in order to meet

company quality objectives and customer commitments.

• Hazmat Emergency Response Team member, responsible in the evacuation,

coordinating clean up and disposal of hazardous waste and materials.

CREE, Durham, NC

June, 2010 – May, 2013.

Process Operator

• Performs operations pertaining to wafer preparation in Surface Prep such as wafer

cleaning, frontside/backside etch, implant, furnace, anneal and oxidation process.

• Inspection of Single Sided Polish wafers.

• Performs cleaning and characterization for process of Power & RF substrates in the SiC

Epilayer Dept.

• 3+ year of Cleanroom experience.



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