Clinical Programmer, FSP - Remote

Overview

The Clinical Programmer at Parexel plays a pivotal role in improving global health through the management and analysis of clinical trial data. This position is dedicated to a single sponsor and offers long-term job security and professional challenges.

In Short

• Responsible for data review and trial management deliverables.
• Program data review listings, reports, and metrics for clinical trials.
• Collaborate with Clinical Data Management and cross-functional teams.
• Develop software systems for efficient clinical data display.
• Create and document software archives and deliverables.
• Provide project planning estimates and record time spent on deliverables.
• Minimum of 5 years of experience in a clinical trial environment.
• Experience with SQL and relational databases.
• Familiarity with CDISC standards.
• Excellent communication skills in English.

Requirements

• Bachelor’s degree in Computer Science, Statistics, Mathematics, or Life Sciences.
• 5+ years of software development experience in clinical trials.
• 3+ years of clinical programming experience.
• Knowledge of data reporting tools specific to clinical trials.
• Experience in the Biotechnology or Pharmaceutical industries preferred.
• Familiarity with programming languages such as SAS, R, or Python is a plus.
• Ability to prioritize multiple assignments effectively.
• Strong familiarity with Microsoft Office products.
• Excellent verbal and written communication skills.

Benefits

• Open and friendly work environment.
• Opportunities for career development and skill enhancement.
• Involvement in significant clinical studies.
• Support from a global team with extensive expertise.
• Long-term job security and professional growth prospects.