Clinical Research Coordinator
3 days ago
**About Medpace**
">MEDPACE IS A FULL-SERVICE CLINICAL CONTRACT RESEARCH ORGANIZATION (CRO). WE PROVIDE PHASE I-IV CLINICAL DEVELOPMENT SERVICES TO THE BIOTECHNOLOGY, PHARMACEUTICAL AND MEDICAL DEVICE INDUSTRIES. OUR MISSION IS TO ACCELERATE THE GLOBAL DEVELOPMENT OF SAFE AND EFFECTIVE MEDICAL THERAPEUTICS THROUGH ITS SCIENTIFIC AND DISCIPLINED APPROACH.
**Job Description**
We are seeking a talented individual to join our Clinical Trial Management team as an Associate Clinical Trial Manager. The successful candidate will work closely with Project Coordinators and Clinical Trial Managers to ensure the timely delivery of clinical trial management activities.
Responsibilities:
- Communicate and collaborate on global study activities;
- Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy;
- Compile and maintain project-specific status reports within the clinical trial management system;
- Interact with the internal project team, Sponsor, study sites, and third-party vendors;
- Provide oversight and quality control of our internal regulatory filing system;
- Provide oversight and management of study supplies;
- Create and maintain project timelines;
- Coordinate project meetings and produce quality minutes;
**Required Skills and Qualifications**
- A PhD in Life Sciences;
- Fluency in English with solid presentation skills;
- Ability to work in a fast-paced dynamic industry within an international team;
- Prior experience within the CRO or pharmaceutical industry not required but will be advantageous;
**Estimated Salary: $80,000 - $110,000 per year**
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