Clinical research positions

- Provide general administrative support to the Clinical Research Department;
- Submission of regulatory documents for non-interventional studies;
- Assist in the organization´s Quality Management System.

- Update of quality documents in accordance with Good Practices;
- Team training;
- Submission of the dossier to the local health authority.

- Development of the Quality Documentation;
- Supply Chain Management;
- Customer Service.

- Receiving, storing, dispensing and returning the IMPs and supplies (IWRS System, accountability log);
- Assist the Principal Investigator and the other members of a clinical trial research team;
- Manage study visits procedures in compliance with GPC and study protocol, phase IV/ type 2 diabetes (Boehringer Ingelheim);
- Ensure the proper record and notification of serious adverse events (SAEs);
- Data entry in the Case Report Forms (eCRFs);
- Provide support in monitoring visits;
- Initiation visits and Investigators ́ meetings participation.

- Medication Reconciliation Program;
- Pharmacovigilance;
- Multidisciplinary teamwork;
- Periodic inventory.

- Telephone service to inform and guide in case of intoxication;
- Provide to the attending physician toxicity information about a specific substance to help in the diagnostic and treatment;
- Pharmacovigilance.

-	Regulatory Framework for Conducting Clinical Research in EU
-	Monitoring methodology for Clinical Trials
-	Data Management	
-	Pharmacoeconomics
-	Market Access
-	Medical Affairs