Drive the clinical operations of assigned studies from Commit to Study Initiation through to study archiving
Craft robust, accelerated delivery plans to ensure timelines and quality standards are met
Lead the Operational Working Group and participate as a key member of the Central Study Team
Ensure compliance with ICH/GCP guidelines and GSK SOPs for assigned studies

Requirements

Bachelor’s degree: life sciences or related discipline
In-depth experience in clinical research: study management, monitoring, data management
Strong skills and experience in project management
Strong performer / executor of operational tasks
Strong understanding of the clinical study, drug development, and quality requirements

Benefits

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools

clinical researchstudy managementmonitoringdata managementproject managementoperational tasksdrug developmentquality requirements

Soft Skills

leadershipcommunicationorganizational skills