Senior Real World Evidence (Statistician) Contractor - Remote

Overview

The Senior Real World Evidence Contractor will play a crucial role in statistical work for observational studies, market access, and clinical trials, working independently while collaborating with various stakeholders.

In Short

• Responsible for scientific and operational statistical work.
• Conducts critical review of study protocols and analysis methods.
• Participates in Study Execution Team meetings.
• Collaborates with multiple stakeholders in various departments.
• Supports development of key study documents.
• Provides input into programming specifications.
• Contributes to study reports and publications.
• Designs and analyzes observational studies.
• Strong programming skills in SAS and R.
• Works effectively in a fast-paced environment.

Requirements

• Master or PhD in Biostatistics or related fields.
• 3 to 7 years of relevant work experience.
• Minimum 2 years of experience in observational studies.
• 3 years of SAS and R programming experience required.
• Ability to multitask and show critical thinking.
• Excellent written and verbal communication skills.
• Ability to collaborate well with non-statisticians.
• Strong work ethic and a 'can-do' mentality.

Benefits

• Work directly with a single sponsor while enjoying global CRO benefits.
• Access to professional development opportunities.
• Supportive work culture focused on quality.
• Diversity and inclusivity in the workplace.
• Opportunity to contribute to meaningful healthcare advancements.