Freshers Associate Statistical Programmer Hiring | Catalyst Clinical Research

 Associate Statistical Programmer | Catalyst Clinical Research | Freshers MSc Statistics

Apply for Associate Statistical Programmer at Catalyst Clinical Research. MSc Statistics freshers or 1-year experience preferred. Apply now!

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Start your journey in clinical data science with Catalyst Clinical Research, a global leader in oncology and multi-therapeutic CRO services. The company is hiring for the position of Associate Statistical Programmer, offering a dynamic opportunity for MSc Statistics graduates and freshers to gain hands-on experience in clinical programming, biostatistics, and SAS development for global pharmaceutical studies.

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Company Overview

Catalyst Clinical Research is a trusted Contract Research Organization (CRO) delivering customized solutions to biopharmaceutical and biotechnology companies worldwide. With its divisions Catalyst Oncology and Catalyst Flex, the organization offers end-to-end clinical development and functional services across multiple therapeutic areas.

Catalyst combines innovative technology, global expertise, and flexible delivery models to accelerate the success of clinical trials. Known for its patient-first approach and scientific rigor, the company is a preferred partner for some of the world’s leading life sciences organizations.

Learn more at CatalystCR.com.

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Job Role & Responsibilities

As an Associate Statistical Programmer, you will be responsible for developing, testing, and validating SAS programs that support statistical analysis and data reporting for clinical studies.

Key Responsibilities:

• Develop and validate SAS programs to produce high-quality clinical trial deliverables within timelines.
• Support data analysis, report generation, and validation for Tables, Listings, and Graphs (TLGs).
• Work with CDISC standards and develop SDTM datasets as per project requirements.
• Collaborate with biostatisticians and data managers to prepare ad hoc analysis reports.
• Utilize PROC REPORT, PROC MEANS, PROC FREQ, PROC TABULATE, and PROC SQL in SAS to handle datasets effectively.
• Implement SAS Macros to automate repetitive tasks and streamline workflows.
• Ensure compliance with company SOPs, regulatory guidelines, and project documentation standards.
• Demonstrate analytical problem-solving abilities and a clear understanding of clinical study protocols and SAPs (Statistical Analysis Plans).

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Eligibility / Qualifications

Educational Background:

• M.Sc. in Statistics, Biostatistics, or Mathematics.

Experience:

• 0 to 1 year of experience in clinical data programming or statistical analysis.
• Freshers with relevant academic projects or SAS training are encouraged to apply.

Technical Skills:

• Strong working knowledge of Base SAS, SAS/SQL, SAS Macros, and SAS Procedures.
• Exposure to R programming or other analytical tools is an advantage.
• Understanding of clinical trial data flow, CRFs, CDISC, and SDTM datasets.

Soft Skills:

• Excellent written and verbal communication skills.
• Ability to collaborate with cross-functional global teams.
• High attention to detail and commitment to quality output.

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Location & Salary

• Location: Remote / Global (based on project allocation)
• Experience Level: Fresher to 1 Year
• Department: Biostatistics / Statistical Programming
• Employment Type: Full-Time, Regular
• Compensation: Competitive salary and performance-linked incentives.

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Application Process

Interested candidates can apply directly through the Catalyst Clinical Research Careers portal.
Ensure your resume highlights your SAS programming experience, statistical projects, or academic coursework in data analytics.

👉 Apply Here – Catalyst Clinical Research Careers Portal

⚠️ Apply early to secure your chance in this competitive opening!

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Why Join Catalyst Clinical Research?

• Work with a leading global CRO focused on oncology and multi-therapeutic research.
• Gain real-world experience in clinical data programming and biostatistical analytics.
• Exposure to CDISC, SDTM, and global regulatory standards.
• Opportunity to work alongside experienced statisticians and clinical data experts.
• Be part of a company that values innovation, collaboration, and continuous learning.

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FAQs

Q1: What qualification is required for the Associate Statistical Programmer role?
An MSc in Statistics, Biostatistics, or a related quantitative field is required.

Q2: Can freshers apply for this position?
Yes, candidates with up to 1 year of experience or strong academic knowledge in SAS and statistics are encouraged to apply.

Q3: What are the primary programming tools used?
Base SAS, PROC SQL, SAS Macros, and R (optional).

Q4: What kind of data will I be working with?
You’ll work with clinical trial datasets, CDISC, and SDTM standards for regulatory submissions.

Q5: Is remote work available for this role?
Yes, based on project requirements and team allocations.

Q6: What are the growth opportunities?
Successful candidates can progress to Statistical Programmer or Biostatistician roles within the organization.

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Summary Table

Category	Details
Company	Catalyst Clinical Research
Vacancy	Associate Statistical Programmer
Required Education	MSc (Statistics, Biostatistics, Mathematics)
Experience	0–1 Year
Location	Remote / Global
Department	Biostatistics / Statistical Programming
Job Type	Full-Time, Regular
Apply Link	Apply Here