Analytical Monitor UK: Data Risk Insights Specialist

QUK IQVIA Ltd.; England; On-site; GBP 40,000 - 55,000; Full time

Job summary

A leading clinical research organization is seeking an Analytical Monitor to oversee data analytics and risk management across multiple clinical trials. The ideal candidate will have a bachelor's degree and over 4 years of experience in the pharmaceutical industry, skilled in data analysis and regulatory guidelines. Strong collaboration with Site Managers and other stakeholders is essential. This role requires effective English communication and is not eligible for UK visa sponsorship.

Qualifications

• 4+ years of experience in Pharmaceutical, CRO or Biotech industry.
• Experience with data analysis.
• Knowledge of clinical drug development and regulatory guidelines (ICH-GCP).
• Ability to collaborate with stakeholders and plan effectively.

Responsibilities

• Conducts activities in compliance with sponsor functional SOPs.
• Facilitates effective communication and manages multiple streams.
• Performs analytical monitoring activities for clinical trials.
• Collaborates closely with Site Managers to action trends.

Skills

Data analysis

Effective communication in English

Collaboration in cross-functional teams

Education

Bachelor's degree in Health Sciences or Data Sciences

Tools

Technology platforms for data collection

Job description

A leading clinical research organization is seeking an Analytical Monitor to oversee data analytics and risk management across multiple clinical trials. The ideal candidate will have a bachelor's degree and over 4 years of experience in the pharmaceutical industry, skilled in data analysis and regulatory guidelines. Strong collaboration with Site Managers and other stakeholders is essential. This role requires effective English communication and is not eligible for UK visa sponsorship.