Clinical Monitoring Analyst (cluepoints) - Remote

IQVIA

Remote
**
Sas programming experience
Cluepoints platform experience
Centralized monitoring plan (cmp)
** IQVIA is seeking a Clinical Monitoring Analyst (CMA) for a remote position that focuses on centralized monitoring processes. The ideal candidate should have strong SAS programming skills, experience in pharmaceutical research, and the ability to work independently while engaging with stakeholders. **

Job Summary

  • This unique role within IQVIA lends itself to a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) with strong communication and organisation skills.
  • The CMA contributes to the execution of the Centralized Monitoring process by performing the setup, programming and refresh(es) of the Centralized Monitoring platform, according to the study-specific Centralized Monitoring Plan (CMP).
  • Main responsibilities include: Supports the Centralized Monitoring Lead (CML) in the development of the fit-for purpose CM strategy by contributing to the identification of the relevant CM elements to be implemented for the study (Quality Tolerance Limits (QTL), Key Risk Indicators, data visualizations and Data Quality Assessments).

Matching Summary

Match Score: 75

** IQVIA is seeking a Clinical Monitoring Analyst (CMA) for a remote position that focuses on centralized monitoring processes. The ideal candidate should have strong SAS programming skills, experience in pharmaceutical research, and the ability to work independently while engaging with stakeholders. **

Skills & Requirements

Must-have

  • SAS programming experience
  • Cluepoints platform experience
  • Centralized Monitoring Plan (CMP)
  • Quality Tolerance Limits (QTL)
  • Key Risk Indicators (KRIs)
  • Data Quality Assessments

Nice-to-have

  • Strong communication skills
  • Organizational skills
  • Problem-solving skills
  • High levels of initiative
  • Collaborative work team participation

Key Requirements

  • At least 3 years relevant experience
  • 2-3 years SAS experience
  • Experience with relational databases
  • Advanced knowledge of federal regulations
  • Good Clinical Practice
  • Good Clinical Data Management Practices

Work Rights

Not specified

Tailored Resume

Cover Letter