Centralized Monitoring Analyst | SAS & Cluepoints Lead

IQVIA; Tees Valley; Remote; GBP 40,000 - 60,000; Full time

Job summary

A leading global provider of clinical research services seeks a Lead Programmer (Centralized Monitoring Analyst) in Tees Valley. This role requires at least 3 years in pharmaceutical research and proficiency in SAS programming. You will support the Centralized Monitoring process and engage with stakeholders. Excellent communication and organizational skills are essential. Note: this role is not eligible for UK visa sponsorship.

Qualifications

• At least 3 years of relevant experience in pharmaceutical research and development.
• 2-3 years SAS experience including macro language.
• Ability to work autonomously and engage with stakeholders.

Responsibilities

• Support the development of CM strategy by identifying relevant elements.
• Setup/Program QTL, KRI and Data Quality Assessments.
• Generate and maintain Centralized Monitoring Platform specifications.

Skills

SAS programming

Communication skills

Organizational skills

Data management

Problem-solving skills

Interpersonal skills

Statistical analysis

Education

3 years relevant experience in pharmaceutical research

Experience with relational databases

Tools

Cluepoints

EDC Systems

Clinical Data Management

Job description

A leading global provider of clinical research services seeks a Lead Programmer (Centralized Monitoring Analyst) in Tees Valley. This role requires at least 3 years in pharmaceutical research and proficiency in SAS programming. You will support the Centralized Monitoring process and engage with stakeholders. Excellent communication and organizational skills are essential. Note: this role is not eligible for UK visa sponsorship.