The role provides critical support to CMS leads in achieving project objectives while optimizing speed, quality, and cost of delivery
Job Summary
The role provides critical support to CMS leads in achieving project objectives while optimizing speed, quality, and cost of delivery.
Incumbents are responsible for reviewing site visit reports, ensuring data integrity, and escalating issues in compliance with ICH/GCP guidelines.
The position requires managing operational insights, performing trend analysis on clinical study metrics, and developing analytics strategies to address clinical risks.
Matching Summary
The role provides critical support to CMS leads in achieving project objectives while optimizing speed, quality, and cost of delivery.
Skills & Requirements
Must-have
Centralized monitoring experience
ICH GCP regulatory compliance knowledge
Clinical trial protocol review skills
Site visit report analysis expertise
Risk assessment and mitigation planning
Nice-to-have
Mentoring junior staff capabilities
Cross-functional collaboration skills
Strong written communication abilities
Therapeutic area knowledge depth
Analytical problem-solving mindset
Key Requirements
Bachelor's degree in Clinical or Life Sciences
Minimum 4 years relevant work experience
At least 2 years in centralized monitor role preferred