Tmf Specialist/documentation Specialist

Description

As TMF SWAT specialist you will be part of a new multidisciplinary team of TMF Advisors & Specialists, who will support global teams to deliver a high quality Trial Master File for our customers. You will have opportunity to work globally and to collaborate with many different teams involved in the management of clinical trials, also presenting you with insights for future career progression.

RESPONSIBILITIES:

 

- Support the management and oversight of TMF activities for paper, electronic and customer TMF systems to ensure delivery of a high quality TMF.  

 
- Conduct review of documents with compliance to Quintiles or customer file plans and SOPs.

  - Serve as a TMF contact for documentation to the project team, and cross functional departments to ensure high quality TMF deliverables are met on time.

 
- Monitor, identify and record quality problems, suggest, initiate, recommend or provide solutions as appropriate. Manage documentation associated with assigned clinical trials.

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

 

- Up to 1 year's project administration experience

 
- Fluency in Italian and English is a must