- Relative Effectiveness Assessment of Pharmaceuticals at national level;- Critical analysis and interpretation of clinical trials and systematic reviews to determine the effectiveness and public funding of health technologies in the NHS; - Liaison with EUnetHTA for JA3 WP7; - Coordination and management of Joint Assessments for EUnetHTA (WP4); - Issuance of certificates related to court matters;- Assessment of Expanded Access Programs;- Upon request, ensure access to… Show more - Relative Effectiveness Assessment of Pharmaceuticals at national level;- Critical analysis and interpretation of clinical trials and systematic reviews to determine the effectiveness and public funding of health technologies in the NHS; - Liaison with EUnetHTA for JA3 WP7; - Coordination and management of Joint Assessments for EUnetHTA (WP4); - Issuance of certificates related to court matters;- Assessment of Expanded Access Programs;- Upon request, ensure access to procedure documents with commercially confidential information redacted; - Provide scientific training (in-house training); - Support external scientific assessors; - Support, update and ensure the availability of information in databases; - Keep up-to-date and aware of new and developing legislation, regulatory policy and technical regulatory guidelines;- Provide regulatory & HTA advice. Show less

Audit, inspect, supervise and conduct disciplinary actions within the health sector for ensuring compliance with the law and with high technical levels of performance in all areas of activity in healthcare carried out either by the services, the institutions and the organizations under the umbrella of the Ministry of Health, or by the private health sector, natural or legal persons aiming profit or nonprofit which are not included in the National Health Service (SNS).

- Collaborate in the Pharmacotherapeutic evaluation of Medicines and Health Products in articulation with CATS (Commission for Health Technology Assessment) and CNFT (National Pharmacy and Therapeutic Committee); - Participation in Joint Action 3 (2016-2019) of the European Network for Health Technology Assessment (EUnetHTA); - Ensure the Executive Secretariat of National Pharmacy and Therapeutic Committee and respective working groups; - Support the preparation and updating of the… Show more - Collaborate in the Pharmacotherapeutic evaluation of Medicines and Health Products in articulation with CATS (Commission for Health Technology Assessment) and CNFT (National Pharmacy and Therapeutic Committee); - Participation in Joint Action 3 (2016-2019) of the European Network for Health Technology Assessment (EUnetHTA); - Ensure the Executive Secretariat of National Pharmacy and Therapeutic Committee and respective working groups; - Support the preparation and updating of the National Medicines Formulary; Show less

- Validation, critical evaluation and management of Marketing Authorisation Variations (Commission Regulation (EC) No. 1234/2008, amended by the Commission Regulation (EU) No. 712/2012);- Validation, critical evaluation and management of renewals (National Procedures);- Revision of proposed SmPC, package leaflets and labelling; - Keep up-to-date and aware of new and developing legislation, regulatory policy and technical regulatory guidelines. Participate in the discussion and… Show more - Validation, critical evaluation and management of Marketing Authorisation Variations (Commission Regulation (EC) No. 1234/2008, amended by the Commission Regulation (EU) No. 712/2012);- Validation, critical evaluation and management of renewals (National Procedures);- Revision of proposed SmPC, package leaflets and labelling; - Keep up-to-date and aware of new and developing legislation, regulatory policy and technical regulatory guidelines. Participate in the discussion and actively contribute to their interpretation and application.- Provide regulatory advice;- Preparation of documents (opinions, memos, proposals for decisions) in accordance with Portuguese and European law and guidelines;- Ensure support for technical and scientific assessors;- Make the communication between the client and the structures of INFARMED, I.P. involved in the different stages of the process;- Establish contacts and exchange of information between medicine authorities of the Member States and European Union bodies;- Issue all the necessary documentation during the ongoing procedure or in its conclusion;- Support, update and ensure the availability of information in databases;- Provide adequate treatment of complaints received and ensure their analysis;- Management of training programs. Show less

Curricular internship in community pharmacy and hospital pharmacy - Dispensing of medicines, pharmaceutical advice, determination of biochemical parameters, pharmaceutical supply, storage and stock management.

Student research fellowship in the field of Protein Folding