Statistical Programmer for Clinical Trials

hace 3 semanas


Bogotá, Bogotá D.E., Colombia PSI CRO A tiempo completo

Company Overview

At PSI CRO, we strive to be the best in our field. With a global presence and over 2,700 dedicated professionals, we bring new medicines to those who need them.

About the Role

This is an exciting opportunity to join our team as a Statistical Programmer for Clinical Trials. You will contribute to statistical programming activities related to global clinical trials, working closely with international teams of statisticians, programmers, and data managers.

Key Responsibilities

  1. Develop analysis data sets structure to support clinical research projects.
  2. Develop program requirements and specifications to meet project needs.
  3. Program data sets and summaries using SAS software (SAS BASE/SAS STAT/SAS GRAPH).
  4. Support SAS program validations to ensure accuracy and reliability.
  5. Prepare and review program documentation to maintain quality standards.
  6. Produce technical reports and communicate effectively with project teams and company departments.

Requirements

  1. You hold a university or master's degree in applied science, mathematics, statistics, or a related field.
  2. You have knowledge of SAS software and experience working in the SAS system.
  3. A strong understanding of programming logic, SQL, and macro programming is preferred.
  4. You are proficient in English, both spoken and written.
  5. You have experience within clinical trials and/or biostatistics.
  6. Good analytical skills are essential for this role.
  7. Proficiency in standard MS Office applications is required.
  8. Excellent communication and interpersonal skills are necessary for success in this position.

Salary

We offer a competitive salary range of $80,000 - $120,000 per year, depending on your qualifications and experience.



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