Associate Clinical Trial Manager – PhD – Oncology – Hematology – Radiopharm
| Company | Medpace, Inc. |
|---|---|
| Location | Irving, TX, USA |
| Salary | $Not Provided – $Not Provided |
| Type | Full-Time |
| Degrees | PhD |
| Experience Level | Entry Level/New Grad |
Requirements
- PhD in Life Sciences
- Fluency in English with solid presentation skills
- Ability to work in a fast-paced dynamic industry within an international team
- Excellent computer (word-processing, databases, Excel, Windows), organizational, and communication skills
Responsibilities
- Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager
- 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.
Preferred Qualifications
- Prior experience within the CRO or pharmaceutical industry not required but will be advantageous