SAS/R Programmer

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Please find the requirement below. If you find yourself comfortable with the requirement please reply back with your updated resume or call me back at

Position : SAS/R Programmer

Location : Remote (Only for EST/CST Candidates)

Duration: 12+ Months Contract

Note : Client won't be able to sponser any visa for this role.

Job Description :

Client has a Remote SAS/R Programmer contract role for a biopharma client.

We are seeking a highly skilled Clinical SAS Programmer with strong R programming experience to join our dynamic team. This role will involve working with clinical trial data, performing statistical analysis, and generating comprehensive reports to support clinical research and regulatory submissions.

**Key Responsibilities:**

1. **Data Management:**

- Develop and maintain SAS programs to import, clean, and validate clinical trial data.

- Use R for data manipulation, analysis, and visualization.

2. **Statistical Analysis:**

- Perform statistical analyses in accordance with study protocols and analysis plans.

- Generate tables, listings, and figures (TLFs) using SAS and R.

3. **Report Generation:**

- Create and QC statistical outputs and clinical study reports for regulatory submissions.

- Document programming activities and ensure compliance with Standard Operating Procedures (SOPs).

4. **Collaboration:**

- Work closely with biostatisticians, data managers, and clinical researchers.

- Provide programming support for ad-hoc analysis requests and exploratory data analyses.

5. **Quality Assurance:**

- Perform rigorous quality checks on all deliverables.

- Maintain annotated datasets and ensure traceability of data processing.

**Qualifications:**

- **Education:** Bachelor's or Master's degree in Statistics, Computer Science, Biostatistics, or a related field.

- **Experience:** Minimum of 3 years of clinical SAS programming experience, with a strong background in R.

- **Technical Skills:**

- Proficiency in SAS and R, including data step programming, PROC SQL, and R packages for data analysis.

- Experience with CDISC standards (SDTM, ADaM).

- Knowledge of clinical trial processes and regulatory requirements (e.g., FDA, EMA).

- **Soft Skills:**

- Strong analytical and problem-solving skills.

- Excellent communication skills, both written and verbal.

Details found in the job post

Retrieved from the description

Developer Role

Data Engineering, Quality Assurance

Technology

R, SQL

Thanks,

Vinay Kumar

Senior Technical Recruiter

VISION INFOTECH INC

Phone:
Email:
368 Main Street, st #3, Melrose MA 02176

E-Verified Company

Regards,

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