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We handle the recruitment process, screening and shortlisting candidates.
Our specialists’ previous employers
HIRE Statistical Programmers (SAS / R)
Clinical SAS Programmer
Aaron D’Souza is a Clinical SAS Programmer with over 8 years of professional experience in clinical data programming, data analytics, and engineering project management. Skilled in SAS (Base, SQL, Macro, ODS, Graph) and experienced with Python (Pandas) and MySQL, Aaron specializes in data extraction, manipulation, and statistical reporting aligned with CDISC and SDTMIG standards. He has a strong understanding of clinical trial data structures, ICH-GCP compliance, and end-to-end data workflows. With proven leadership and analytical skills, Aaron consistently delivers high-quality, timely outputs while ensuring regulatory and technical precision across clinical projects.
AutoCAD
Base SAS
CDISC
Clinical Data Management Tools
HVAC Design & Validation Tools
ISO Documentation
MS Office
MySQL
SAS
SAS 9.3
SAS/GRAPH
SAS/Macro
+3 More
Senior Statistical Programmer
Nathan George is a Senior Statistical Programmer with over 9 years of experience in clinical research and statistical programming. Skilled in SDTM, ADaM, and TLF development, he specializes in programming, validation, and data mapping to support clinical trial analysis and regulatory submissions. Nathan has worked with leading organizations including Novartis, Bayer, QuintilesIMS, and St. John’s Research Institute, delivering high-quality statistical outputs aligned with FDA, DCGI, and EC standards. Proficient in Argus Safety, WHO Drug Dictionary, and MedDRA coding, he combines technical expertise with strong analytical and mentoring skills to ensure data integrity and compliance across global studies.
ADaM
Argus Safety
CDISC Standards
Clinical Reporting Tools
MedDRA
Metadata Documentation
MS Office
SAS
SDTM
TLF
WHO Drug Dictionary
Sr. Associate Manager – Data Analyst
Data-driven professional with 9 years of experience specializing in SAS and SQL programming within the clinical data management and analytics domain. Skilled in data validation, automation, reporting, and visualization using SAS, R, and Power BI. Adept at process optimization, developing automation utilities, and providing technical leadership. Strong foundation in CDISC, SDTM, and ADaM standards, with experience guiding data teams and improving operational efficiency through automation and SOP development.
ADaM
CDISC
Power BI
R
R Studio
SAS (Base & Advanced)
SAS EG 8.1
SDTM
SDTMIG
SQL
TOAD for Oracle
Senior Statistical Programmer – II
Results-driven professional with 11 years of experience in clinical research, including over 5.6 years in statistical programming. Skilled in SAS (Base, SQL, Macro) and R programming for clinical data analysis, development of SDTM and ADaM datasets, and generation of TLFs per study specifications. Demonstrated expertise in clinical trial data across Phases I–III, regulatory documentation, and cross-functional collaboration. Certified in Lean, Green Belt, and Six Sigma, with strong experience in KPI management, process improvement, and client interactions.
ADaM
Aris-G
CDISC (SDTM
Data Validation
KPI Management
Macros)
Process Automation
R
R Studio
regulatory compliance
Safety Data Analytics
SAS
+4 More
Senior Statistical Programmer
Results-oriented Senior Statistical Programmer with 8+ years of experience in clinical trial programming, statistical analysis, and data management. Skilled in developing ADaM, SDTM, and TLF datasets across oncology, immunology, and vaccine studies. Adept at regulatory submissions, process automation, and cross-functional collaboration. Proven leadership and mentoring abilities, with expertise in compliance (P21, 21 CFR Part 11) and advanced data visualization techniques.
21 CFR Part 11
ADaM
Advanced
CDISC
Clinical Data Repositories
GCP
GPP
Macros)
P21 Validator
R
R (Beginner)
SAS
+3 More
SHARED EXPERIENCES
"F5 BioTalent made hiring painless. Within days, we onboarded specialists who integrated seamlessly with our workflows."
Emily Sanchez
COO, Growth-Stage Biotech
We handle the recruitment process, screening and shortlisting candidates.
therapeutic area, function, tools, time zone, start date.
I’m looking for:
Clinical Data Manager
Skills
Clinical Data Manager
Medical Writer
Regulatory Specialist
Biostatistician
Suggested
Data Engineer / Data Scientist
AI Drug Discovery Engineer
Data QC Specialist
screening, assessments, and shortlists; you interview finalists.
Interview
Arjun Mehta
we handle contracting, onboarding, and ongoing support.
Bioinformatics
Clinical Operations
Pharmacovigilance
+5 Other
Employment Contract
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Expertise
Clinical Data Manager
Medical Writer
Regulatory Specialist
Biostatistician
Data Engineer / Data Scientist
+9 more
F5 BioTalent™
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Vetted Specialists
250+
Global Biotech Partners