Lurdes Morgado Email & Phone Number

Mafra, Pt

I am responsible for lymphoma and chronic myeloid leukemia, among other hematological diseases where there are drugs in pipeline.I am also responsible, within the oncology area, for targeted therapies in the biliary duct cancer among others in pipeline.

- Identify, develop, and maintain relationships with current and future Key Opinion Leaders (KOL), Portuguese MM Group and Cooperative Groups.- Develop and implement local medical affairs plan according to global medical affairs plan and to local marketing plan. - Plan and organize symposiums for the national hematology congress (SPH) with important KOLs. - Plan, design and execute advisory boards at a regional/national level.- Implement and disseminate high quality medical and… Show more - Identify, develop, and maintain relationships with current and future Key Opinion Leaders (KOL), Portuguese MM Group and Cooperative Groups.- Develop and implement local medical affairs plan according to global medical affairs plan and to local marketing plan. - Plan and organize symposiums for the national hematology congress (SPH) with important KOLs. - Plan, design and execute advisory boards at a regional/national level.- Implement and disseminate high quality medical and scientific educational programs. - Provide medical information to unsolicited requests to internal and external stakeholders.- Clinical Trials Worldwide Field Medical Lead, communicating with WW MSLs and global team- Foster Clinical Research, supporting clinical research operations and the trial participating sites and support Investigator-Initiated Trials (IITs) and Non-Interventional Studies (NIS).- Coordinate and executes internal training to Key Account Managers (KAM), Sales Representatives (SalesRep), Product Managers (PM) and Market Access.- Revision and approval of marketing and medical materials from medical perspective. Show less

Lisbon Area, Portugal

Reporting to the Oncology Business Unit Director I was responsible to:- Hire and thereafter coordinate the Clinical Research Associate (CRA) responsible for the implementation and monitoring the company sponsored clinical trials.- Develop a solid partnership with Key Stakeholders to discuss relevant scientific data, generate and implement key medical projects.- Contribute to strategic decisions regarding products.- Respond to medical information inquiries concerning disease and… Show more Reporting to the Oncology Business Unit Director I was responsible to:- Hire and thereafter coordinate the Clinical Research Associate (CRA) responsible for the implementation and monitoring the company sponsored clinical trials.- Develop a solid partnership with Key Stakeholders to discuss relevant scientific data, generate and implement key medical projects.- Contribute to strategic decisions regarding products.- Respond to medical information inquiries concerning disease and company products.- Collaborate with investigators to identify potential research opportunities.- Support marketing and sales teams with new scientific and medical information about market and clinical research of oncology products.- Training of sales representatives and Clinical Research Associate (CRA). Show less

- Responsible for managing the assigned clinical projects from different therapeutic areas (Hepatitis C Virus, Human Immunodeficiency Virus, Anti-Infectives, Vaccines-Oncology/Hematlogy, Reumatology, Parkinson Disease, Diabetes) within the country from pre-validation to close-out phases to ensure its successful execution.- Responsible for contacting Key Opinion Leaders in order to inform them about the MSD Book of Business in the context of clinical projects with new molecules.-… Show more - Responsible for managing the assigned clinical projects from different therapeutic areas (Hepatitis C Virus, Human Immunodeficiency Virus, Anti-Infectives, Vaccines-Oncology/Hematlogy, Reumatology, Parkinson Disease, Diabetes) within the country from pre-validation to close-out phases to ensure its successful execution.- Responsible for contacting Key Opinion Leaders in order to inform them about the MSD Book of Business in the context of clinical projects with new molecules.- Responsible to perform the study submissions to Central Ethics Committee (CEIC), Health Authority (INFARMED) and Data Privacy Committee (CNPD) and development of the country informed consent forms.Main Projects and Achievements- Interaction with medical affairs and marketing and sales departments with added value.- Regional Clinical Project Manager for Switzerland for management of a study managing remotely the Clinical Research Associates and Clinical Trial Coordinators, consolidating my ability to effectively collaborate with affiliates.- Change Agent Role winning an award of excellence. - Organization and speaker at Local Investigators Meetings. - Rapid cycle times to initiate the study at the investigational sites, aggressive recruitment plans, recruitment predictability within target with good mitigation plan to recover recruitments, if needed.- Personally involved in study validations before the projects are allocated to Portugal.- Mentored successfully CRAs in the CPM function who showed results in managing the studies assigned. Show less

- Responsible for implementing and monitoring clinical trials phase 2/3/4 from different therapeutic areas (rheumatology, allergology, cardiology, Hepatitis C Virus, Hematology/Oncology), reporting directly to medical director.- Responsible for the study submissions to CEIC, INFARMED and sites and development of the country informed consent forms

- Responible for the report of adverse events into Schering-Plough reporting system according to timelines set forth in global, European and local SOPs - Responsible to provide training on a regular basis to all Schering-Plough employees

- Responsible for implementating and monitoring clinical trials phase 2/3/4 in cardiology, dermatology and neurology area, reporting directly to Madrid. Speaker at Investigator Meeting.

- Responsible for implementation and monitoring clinical trials phase 3/4 in cardiology area.

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