- Provide quality review of the Informed Consent Form and other study documents. - Compile Part ll documents for Country Submissions under new EU CTR regulation via CTIS platform.- Negotiate and follow up contracts with sites until they are fully executed according to the study protocol and budget.- Ensure all the required documents are filed in eTMF according to the study requirements.- Follow up with sites in Start Up and study vendors until investigator teams are trained and ready to start recruitment.- Provide the client with a constant view of the development of the study and adjust to their needs and timelines.

- Learning and adoption of RSU Maintenance activities: RA/EC substancial amendments and notifications.- Negotiates and follow up contracts amendments with sites until they are fully executed according to the protocol and study budget.- Manages filing of clinical trial documents in eTMF and tracking in study platforms.

- Medication management and pharmaceutical counselling.- Management of pharmaceutical computer programs such as Farmatic. - Learnings in dermopharmacy and cosmetics.

- Provide quality service to all our guests.- Setting up work stations, preparing and assembling menu items to specification.- Prepare recipes, stock areas with supplies using “FIFO” method, check quality of products.- Keep work stations presentable for guests.

- Study of mechanisms of action of neuroprotective substances.- Safety and toxicity studies of new molecules in cell cultures.