Job Summary
Our European activities are growing rapidly, and we are currently seeking a full-time Project Assistant in either London, England or Stirling, Scotland, UK to join our Regulatory Affairs team, supporting two of our key sub-teams within the department:
* The central labeling team in development of clinical trial labels.
* The regulatory intelligence team to help maintain a central database.
This fully office-based administrative assistant position will provide daily administrative support to the teams to accomplish tasks and projects that are instrumental to the company’s success. If you want a new role with a stable organization then this is the opportunity for you.
Responsibilities
* Member of a small team managing the label review, country adaptation and translation process.
* Creating country specific labels in English, using our in-house database.
* Coordinating multiple translations with our vendor companies and local associates.
* Interacting with Medpace staff globally to finalize label reviews.
* Tracking progress and working to deadlines on multiple projects.
* Performing quality control of labels.
* Coordinating and providing minutes for departmental meetings/conference calls.
* Performing other tasks as needed.
Qualifications
* Experience in a detailed administrative role preferred.
* Minimum of a high school diploma.
* Great attention to detail.
* Ability to work well in a team environment.
* Excellent organizational and prioritization skills. Work experience in a health science setting preferred.
* Excellent oral and written communication skills in English language.
* Knowledge of Microsoft Office.
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
EO/AA Employer M/F/Disability/Vets
#J-18808-Ljbffr