Job Summary : Responsibilities :

• Engage in clinical trial management on a day to day level;
• Work closely with the project CTM for timely delivery of recurrent tasks consistently with a high degree of accuracy;
• Compile and maintain project-specific status reports;
• Update CTMS with study milestones, enrolment projections etc.
• Update e TMF and perform ongoing e TMF QC;
• Support clinical trial manager to draft study plans and study specific guidance documents;
• Manager site feasibility, site activation preparation and study supply managements;
• Communicate with regional cross functional team, vendors and sponsor effectively;

Qualifications :

• Bachelor's degree in a health sciences field;
• Maintain thorough knowledge of project and ability to coordinate/present at internal/external meetings and conference calls;
• Excellent computer (word-processing, databases, Excel, Windows) and organizational skills.

Medpace Overview : Why Medpace? :
Medpace Perks

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility