Lead Centralized Monitoring Analyst (SAS/Cluepoints)

QUK IQVIA Ltd.; City Of London; Remote; GBP 50,000 - 70,000; Full time

Job summary

A leading clinical research organization is seeking a Lead Programmer (CMA) with strong SAS programming and data management skills. This role requires at least 3 years in pharmaceutical research and involves direct client communication, managing the Centralized Monitoring process. The ideal candidate will have experience with Cluepoints and demonstrate excellent initiative and problem-solving capabilities.

Qualifications

• At least 3 years of relevant experience in pharmaceutical research.
• 2-3 years SAS experience including macro language.
• Knowledge/experience working on Cluepoints.

Responsibilities

• Support the Centralized Monitoring Lead in developing CM strategy.
• Setup/Program QTL, KRI, and Data Quality Assessments.
• Generate and maintain Centralized Monitoring Platform specifications document.

Skills

Communication skills

Organizational skills

SAS programming

Data management

Statistical analysis concepts

Confidentiality maintenance

Problem-solving skills

Tools

Cluepoints

Clinical Data Management Systems

EDC Systems

Job description

A leading clinical research organization is seeking a Lead Programmer (CMA) with strong SAS programming and data management skills. This role requires at least 3 years in pharmaceutical research and involves direct client communication, managing the Centralized Monitoring process. The ideal candidate will have experience with Cluepoints and demonstrate excellent initiative and problem-solving capabilities.