In the competitive field of clinical research and pharmaceutical analytics, a well-crafted resume can set you apart. Whether you're a fresher or transitioning from a related field, having an ATS-compliant, detailed, and skills-focused resume is crucial. This guide provides resume examples and insights to help you secure a Clinical SAS Programmer role in 2025.

1. Resume Sample for Fresher

John Doe

Email: [email protected] | Phone: +91-9876543210 | Location: Bangalore, India | LinkedIn: linkedin.com/in/johndoe

Objective:

Detail-oriented and highly motivated individual with a strong foundation in Clinical SAS programming. Successfully completed a hands-on project on Clinical SAS using oncology data at Handson School of Data Science. Seeking an entry-level Clinical SAS Programmer role to contribute to pharmaceutical research and clinical trials.

Education:

• Postgraduate Diploma in Clinical Research & SAS Analytics – Handson School of Data Science, 2024
• B.Sc. in Biotechnology – XYZ University, 2023

Technical Skills:

• SAS Base & Advanced (SAS Macros, PROC SQL, Data Step)
• Clinical Data Management & Reporting
• SDTM, ADaM, CDISC standards
• Statistical Analysis & TLF generation

Live Project:

• Project: Oncology Data Analysis for Clinical Trials
• Description: Processed and analyzed oncology clinical trial data to create SDTM datasets, ADaM datasets, and TLFs under FDA compliance.
• Tools Used: SAS Base, SAS Macros, PROC SQL

Certifications:

• SAS Certified Base Programmer
• CDISC SDTM &ADaM Training

Soft Skills:

• Analytical Thinking
• Attention to Detail
• Team Collaboration

2. Resume Sample for Professionals from CRO/Pharmacovigilance/Medical Coding

Jane Smith

Email: [email protected] | Phone: +91-9876543211 | Location: Hyderabad, India | LinkedIn: linkedin.com/in/janesmith

Objective:

Experienced Pharmacovigilance Analyst with 3+ years of expertise in safety data management and adverse event reporting. Recently trained in Clinical SAS programming to transition into statistical programming roles in clinical research. Looking for opportunities in a CRO or pharmaceutical company.

Education:

• Advanced Certification in Clinical SAS Programming – Handson School of Data Science, 2024
• M.Pharm in Pharmacology – ABC Institute of Pharmaceutical Sciences, 2021

Technical Skills:

• SAS Base & Advanced (PROC REPORT, PROC MEANS, SAS Macros)
• Adverse Event Data Processing
• Regulatory Compliance (ICH-GCP, FDA guidelines)
• MedDRA, WHODrug Coding
• SDTM &ADaM Standards

Work Experience:

XYZ CRO Pvt. Ltd. – Pharmacovigilance Analyst (2021 – Present)

• Managed case processing for adverse event reports using Argus Safety
• Collaborated with clinical teams to ensure accurate safety data submission
• Performed signal detection using SAS statistical procedures

Live Project:

• Project: Adverse Event Data Analysis for Regulatory Submission
• Description: Utilized SAS to analyze adverse event reports and generate summary tables compliant with CDISC standards
• Tools Used: SAS, Argus Safety, SQL

Certifications:

• SAS Certified Clinical Trials Programmer
• Good Pharmacovigilance Practices (GVP) Training

Soft Skills:

• Data Analysis
• Regulatory Compliance
• Communication Skills

3. Resume Sample for Biotechnology/Biostatistics/Quality Control Professionals

Rahul Verma

Email: [email protected] | Phone: +91-9876543212 | Location: Mumbai, India | LinkedIn: linkedin.com/in/rahulverma

Objective:

Biotechnology professional with 4+ years in quality control and clinical data analysis, recently transitioned into SAS Clinical Programming. Seeking a role in statistical programming and clinical research data management.

Education:

• Professional Diploma in Biostatistics & SAS Programming – Handson School of Data Science, 2024
• M.Sc. in Microbiology – DEF University, 2020

Technical Skills:

• SAS Programming (Data Step, PROC SQL, PROC MEANS, PROC UNIVARIATE)
• CDISC SDTM &ADaM Mapping
• Statistical Modeling& Data Analysis
• Quality Control & Compliance in Clinical Trials

Work Experience:

ABC Biopharma Ltd. – Quality Control Analyst (2020 – Present)

• Ensured regulatory compliance for drug formulation and safety testing
• Conducted biostatistical analysis for product quality validation

Live Project:

• Project: Clinical Data Analysis for Drug Safety in Microbiology Research
• Description: Performed SAS-based statistical analysis on microbiological clinical trial data, prepared reports for regulatory review
• Tools Used: SAS, Excel, R

Certifications:

• SAS Certified Biostatistics Programmer
• Good Clinical Laboratory Practice (GCLP) Certification

Soft Skills:

• Data Interpretation
• Statistical Analysis
• Problem-Solving

Conclusion

These sample resumes showcase how professionals from different backgrounds—freshers, pharmacovigilance analysts, medical coders, biostatisticians, and microbiologists—can transition into Clinical SAS programming.

If you are looking to upskill and start a rewarding career in Clinical SAS, visit Handson School of Data Science to explore industry-focused training programs.