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Statistical Programmer Analyst

0-1 years
Not Disclosed
10 Oct. 8, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Join Fortrea: Junior Statistical Programmer

As a leading global contract research organization (CRO), Fortrea is dedicated to scientific excellence and boasts decades of experience in clinical development. We offer pharmaceutical, biotechnology, and medical device clients a comprehensive range of clinical development, patient access, and technology solutions across over 20 therapeutic areas. With more than 19,000 employees operating in over 90 countries, Fortrea is transforming the landscape of drug and device development for partners and patients worldwide.

Job Overview

We are seeking a Junior Statistical Programmer to support our Statistical Programming services. In this role, you will develop SAS (Statistical Analysis System) programs and outputs to manage and report clinical trial data.

Key Responsibilities

  • Provide statistical programming services, developing SAS programs for clinical trial data management and reporting.

  • Create programs for data transfers according to client specifications.

  • Review draft and final production runs to ensure quality and consistency.

  • Ensure the quality of your work and engage with project team members across Clinical Data Management, Clinical Operations, and Biostatistics.

  • Manage your workload effectively to meet deadlines.

  • Foster a positive team spirit in a professional environment.

  • Continuously enhance your skills and problem-solving abilities.

  • Adhere to Fortrea’s Standard Operating Procedures (SOPs) and Good Clinical Practice (GCP) guidelines.

  • Perform other duties as assigned by senior Statistical Programming staff.

Preferred Qualifications/Experience

  • Bachelor’s degree in computing, life sciences, mathematics, or a related statistical field.

  • 0–1 year of programming experience using SAS; foundational programming knowledge is essential.

  • Mandatory SAS certification.

  • Basic understanding of the clinical trial process.

  • Strong time management skills and ability to prioritize work effectively.

  • Excellent communication skills and a cooperative, team-oriented approach.

  • Self-motivated with a focus on quality and results.

Fortrea seeks motivated problem-solvers and creative thinkers who are passionate about overcoming barriers in clinical trials. Our commitment to revolutionizing the development process ensures the swift delivery of life-changing therapies to patients in need. Join our exceptional team and experience a collaborative environment that nurtures personal growth, enabling you to make a meaningful impact globally.

Fortrea is an Equal Opportunity Employer. We embrace diversity and inclusion, making employment decisions based solely on business needs and individual qualifications. We do not discriminate based on race, religion, gender, age, disability, or any other legally protected characteristic. We encourage all qualified candidates to apply.

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