Job title: Clinical project coordinator (medpace)

Roles and Responsibilities

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 eTMF and perform ongoing eTMF 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 life 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.