Daniel Brás Email & Phone Number

Lisbon, Portugal

Lisbon, Portugal

As RWE Lead, my main responsibilities were:• Lead integrated planning and execution of RWE strategies at a country level, from the inception and development of concepts and protocols, through to the implementation of studies and publication, with a focus on Oncology and Hematology areas.•Aligned RWE initiatives strategically through cross-functional collaboration to address data and evidence gaps, contributing to timely reimbursement approvals, contract renegotiations, and enhancing the value proposition of Novartis brands.• Collaborate with internal and external stakeholders to generate evidence and confirm value, ensuring broad and sustainable access to Novartis marketed brands and future pipeline assets.• Evaluate the strengths and limitations of external data sources within each therapeutic field to continuously enhance real-world data initiatives.• Actively contributed to the development of the company’s local RWE strategy and vision, fostering strategic external partnerships (such as academia or NHS) to drive health system improvements through RWE initiatives.

Lisbon, Portugal

Working in an Agile structure I play a three part role within the organization as Disease Area Lead for Rare Hematology brands, Project Onwer (focused on Real World Evidence) and Market Access Manager. Reporting to the Oncology Market Access Head, my main responsibilities as Market Access Manager are:- Leading the implementation of a sustainable Patient Access strategy at a local level for hematology portfolio;- Collect and analyze data to generate insights for Patient Access submissions that jointlycreate value for customers, patients and the company- Lead projects to submit patient access dossiers to regulatory authorities applying highstandards of operational excellence-Co-lead RWE projects that will support dossier submissions to HTAs-Build and leverage strong networks and relationships with key customers, key opinionleaders and individual and institutional key decision makers, to optimize the positioningand messaging of Novartis products and facilitate the co-creation of value propositionswith customers.-Leads the local input to both global and local Pricing-Adapt Global Healthcare Economic models to accurately reflect local environments

Lisboa E Região, Portugal

Reporting to the Oncology Medical Director, my main responsibilities are:As Medical Advisor, give the medical support to the Hematology Franchise in Polycythemia Vera & Myelofibrosis, GvHD and Sickle Cell DiseaseCo-Lead cluster team to prepare the presence and new launch in Sickle Cell Disease, in Portugal, Belgium and the Netherlands, having full alignment on successful launch strategy and requirementsLeading the mapping process of key stakeholders such as KOLs and Patient Advocacy membersDevelop integrated Public Relation strategy for Sickle Cell Disease therapeutic areaClose support in the development of local market access strategies building together key projects to fill the data gaps (according with budget) and leverage product value proposition - such as value dossier or business impact tool tailored to the process needsEnsure readiness for local Early Access Programs implementation, allowing early access to patients

Milan Area, Italy

Supporting RE Marketing Head for Breast Cancer. Reporting to Pipeline Strategy Director, I have supported a new launch in Breast Cancer. In this assignment I was able to support:The implementation of a Regional Europe Commercial Advisory Board, to understand how to best communicate the implications of the PIK3CA mutation, obtain advice on the best position and sequencing for the new product and to collect insights on the marketing strategyImplementation of Virtual Workshop with early launching countries from Region Europe, to understand countries’ needs, identification of synergies, key data gaps, generation and selection of the best tacticsThe cross-functional team in the preparation and content alignment for deep dive meeting with RE Oncology Leadership Team

Lisbon

As Medical Advisor, my major responsibilities are:- To provide a source of key medical and scientific knowledge on the company's products- To collaborate with Country, Regional and Global team members in the execution of relevant clinical activities in assigned projects (eg. Identification of potential study sites and support study accrual for key trials as appropriate, provide feasibility and research site recommendation for company sponsored clinical trials);- Upon investigator request, liaise between potential researcher and the Company on Investigator Initiated Trials process- To design, initiate, conduct and publish local Non-Interventional/Phase IV studies in the company to help facilitate market access and adoption within country- To pair key stakeholders' scientific educational and research needs with available company resources and provide the latest emerging data in response to specific HCP inquiries, as appropriate.- To provide and discuss medical, scientific and health care and outcome research evidence on new treatment options, Novartis compounds, products, therapeutic and research areas with key HCPs and relevant stakeholders involved in patient treatment decisions.- To raises awareness of company products / cardiometabolic desease area through the publication of manuscripts, presentations and training- To contributes to shape the brand plan proactively providing external stakeholders’ insights and contribute to the design and execution and the Medical Affairs strategy and plan

Lisbon Area, Portugal

With focus on Heart Failure and Hypertension disease areas, my responsibilities are: - To develop peer to peer scientific relationships, assess advocacy and contributions, and respond to unsolicited requests for scientific information with Medical Experts and Key Stakeholders; - Strategically prepare and support the development, launch and commercialization of new products on Cardiovascular Therapeutic Area through scientific exchange, seeking external insight in order to understand the therapeutic environment; - Respond to unsolicited requests for scientific information about commercialized products and drugs under development; - Contribute to the identification and mapping of Medical Experts/key stakeholders for the Cardiovascular Therapeutic Area; - Provide speakers' training to HCPs to support education to the healthcare community about commercialized therapies; - Provide feasibility, research site recommendation along with local clinical trials’ team and support ongoing clinical trials; - Implement scientific projects according to global, regional or local medical strategies; - Provide medical support and training to internal teams (ex: sales reps).

Lisbon, Portugal

Lisbon, Portugal

Ensure that DLA Farmacêutica complies with implemented procedures approved by INFARMED;Ensure that DLA Farmacêutica meets the Quality and Safety standards;Logistic Manager of "Laboratórios Azevedos" - Daily contact with National and International suppliers;Permanent Team-Work with "Laboratórios Azevedos" Regulatory Affairs and Business Units;

Paço De Arcos

Stock Management;Human Resources Management;Procurement and decision making in supply agreements.

Prescription validation, daily laboratory analyses interpretation and clinical visit of General Surgery’s patients;Elaboration of Pharmacokinetic Protocols (Vancomycin, Gentamicin, Amikacin and Caffeine Citrate);Unitary Dose Dispense and Hospital Pharmacy warehouse manager;In charge of Haemoderivates and Psicotropic circuit;Accountable for ambulatory drug dispense and remaining clinical services when scheduled.

R&D project in an EDOL laboratories and Faculty of Pharmacy Partnership

Phd Student, Epidemiology, Phd

Master, Pharmaceutical Sciences, Pharmd

Activities and Societies: Organization and foundation of University Catholic Missions R&D project in an EDOL laboratories and Faculty.

Education record