Lester Domínguez Email and Phone Number

. Predict the development trend of life science, point out research hotspots and guide work, construction and development of Life Research journal.2. Provide or recommend at least one high-quality manuscript (Research article or Review) to the journal every year based on your own situation.3. Actively participate in the manuscript review and reply to the review comments as soon as possible (within 2 weeks).4. Take an active part in the promotion of journals by using your own advantages or other platform advantages to spread the articles and knowledge.Achievements:Submitting articles. Administering peer review or serving as a peer reviewer. Helping the journal to attract high-quality manuscripts, for example by promoting the journal at relevant conferences. Providing feedback and suggesting improvements for the journal.

• Lead various projects assigned to Peru, Colombia and Guatemala.• Supervise and monitor the implementation of projects in research centers, for compliance with Good Clinical Practices (SOPs) and study sponsors.• Recruit researchers for participation in clinical trials.• Design and apply the strategic management of the assigned projects, communicating the progress with the different interlocutors of the project.• Verify compliance with the quality control of the assigned Projects and translate them into the preparation of respective reports on findings.• Manage communication with Stakeholders in the Clinical Research area (Ethics Committees, National Institute of Health, etc.).• Responsible for supervising the activities of clinical operations team members.• Planning, organizing, and directing the activities of personnel involved in clinical research projects to make sure that they are in line with general clinical goals and objectives.• The management of all aspects of clinical trial and the selection of vendors so as to guarantee the safety of patients, non-breaching of contract, procedures, and data integrity.• Responsible for the preparation and review of all documents that are related to clinical projects, which includes contracts, vendor budgets, and annual reports.• Review and approve invoices being presented by study vendors and external consultants• Answerable to questions and issues brought up by vendors and external consultants• Help in the training and development of clinical staff as at when due• Lead the clinical project team and various study team meetings• Oversee the pattern and way clinical research study is being conducted• Fully involved in resolving issues; take part in procedure improvement initiatives• Attain clinical study’s goals by working with other members of the study team to outline their priorities, and to also resolve conflicts that may come up in the project process• Work together with clinical trial managers

• Lead various projects assigned to Peru, Brazil, Ecuador Mexico, and Sud Africa.• Supervise and monitor the implementation of projects in research centers, for compliance with Good Clinical Practices (SOPs) and study sponsors.• Recruit researchers for participation in clinical trials.• Design and apply the strategic management of the assigned projects, communicating the progress with the different interlocutors of the project.• Verify compliance with the quality control of the assigned Projects and translate them into the preparation of respective reports on findings.• Manage communication with Stakeholders in the Clinical Research area (Ethics Committees, National Institute of Health, etc.).• Responsible for supervising the activities of clinical operations team members.• Planning, organizing, and directing the activities of personnel involved in clinical research projects to make sure that they are in line with general clinical goals and objectives.• The management of all aspects of clinical trial and the selection of vendors so as to guarantee the safety of patients, non-breaching of contract, procedures, and data integrity.• Responsible for the preparation and review of all documents that are related to clinical projects, which includes contracts, vendor budgets, and annual reports.• Review and approve invoices being presented by study vendors and external consultants• Answerable to questions and issues brought up by vendors and external consultants• Help in the training and development of clinical staff as at when due• Lead the clinical project team and various study team meetings• Oversee the pattern and manner in which clinical research study is being conducted• Fully involved in resolving issues; take part in procedure improvement initiatives• Attain clinical study’s goals by working with other members of the study team to outline their priorities, and to also resolve conflicts that may come up in the project process

Participation in teaching the practical and theory sessions of the following courses in the Department ofPharmacy and Biochemistry, Faculty of Pharmacy and Biochemistry:- Biochemistry for post graduates- Pharmacology for post graduates- Talent Management for post graduates- Physiopathology for post graduates- Semiology for post graduates- Morphophysiology for post graduates

• Supervision and monitoring of the projects of students of the Faculty of Human Medicine, Faculty of Physical Medicine and Rehabilitation, Faculty of Nursing, Faculty of Obstetrics, Faculty of Pharmacy and Biochemistry in the course of physiology and pharmacology, verifying the compliance of the Good Clinical Practices according to standardized operating procedures of the Institution.• Responsible for Pre-degree courses in physiology, pharmacology.• Review of the database of scientific bibliography and the interpretation of its validity for complementation of the work of the students

Contribuir en la prevención de las enfermedades causadas o relacionadas con el trabajo, desarrollando acciones de vigilancia médica para proteger y promover la seguridad y salud en el trabajo de los servidores del Programa Nacional para la Prevención y Erradicación de la Violencia contra las Mujeres e Integrantes del Grupo Familiar.

Sub investigator for Clinical Trial Phase I study.Medical Scientist and Supervision and monitoring of the implementation of projects in research centers for compliance with Good Clinical Practices according to standardized operating procedures by the Company (SOPs) and the study sponsors.Writing Effective SOPs for CLIA Lab SABELL Laboratory S.A.C. according to the FDA regulations.

Post-graduate Professor of the Master of Health Management for the Course: Thesis Seminar II.Functions:• Supervision and monitoring of the projects of students of the Master of Health Management, verifying compliance with Good Clinical Practices according to standardized operating procedures of the Institution.• Responsible for the Thesis Seminar II Course.• Review of the database of scientific bibliography and the interpretation of its validity for complementation of the work of the students

• Lead various projects assigned to Peru.• Supervise and monitor the implementation of projects in research centers, for compliance with Good Clinical Practices (SOPs) and study sponsors.• Recruit researchers for participation in clinical trials.• Design and apply the strategic management of the assigned projects, communicating the progress with the different interlocutors of the project.• Verify compliance with the quality control of the assigned Projects and translate them into the preparation of respective reports on findings.• Manage communication with Stakeholders in the Clinical Research area (Ethics Committees, National Institute of Health, etc.).

Customer Served: Pfizer• Lead various projects assigned to Peru and Ecuador.• Supervise and monitor the implementation of projects in research centers, for compliance with Good ClinicalPractices (SOPs) and study sponsors.• Recruit researchers for participation in clinical trials.• Design and apply the strategic management of the assigned projects, communicating the progress with the differentinterlocutors of the project.• Verify compliance with the quality control of the assigned Projects and translate them into the preparation ofrespective reports on findings.• Manage communication with Stakeholders in the Clinical Research area (Ethics Committees, National Institute ofHealth, etc.).• Mentoring Junior CRAs and regulatory process personnel.Achievements:• I corrected the observations of an important project that reassigned my person, managing to reduce during the firsttwo months 80% of the observations presented in the 10 monitored centers, including incomplete data, registrationof monitoring reports and follow-up letters to researchers, etc. Through adequate follow-up and a good relationshipwith researchers.• I improved the communication circle with the sponsor, proposing to make reports on a weekly basis, that is, doublingtheir frequency, to reinforce their positive perception in the management of the project and to demonstrate theimprovement actions in it. Achieving favorable comments on his visit to two centers.I improved the quality and delivery times of laboratory analyzes, through a review of a legacy project, evidencing possible incidents and preventing their observations, managing the change of clinical laboratory at a good cost, managing to work with a clinical laboratory that met all international ISOS certifications.

Customer served: Pfizer, Roche, Grunenthal, Genentech, AstraZeneca, GlaxoSmithKline, Regeneron Pharmaceuticals, Sanofi-Aventis, Merck & Co., Novartis, Celgene, Amgen, Genzyme, Gilead Sciences.• Supervise and monitor the implementation of projects in research centers for compliance with Good Clinical Practices, according to standardized operating procedures by the Company (SOPs) and the study sponsors.• Recruit researchers for participation in clinical trials and the respective negotiation of budgets.• Verify compliance with the quality control of the assigned Projects and prepare the respective reports on findings.• Prepare project management reports for clients, assigned monitors, and Company personnel.• Perform communication management with Stakeholders in the Clinical Research area (Ethics Committees, National Institute of Health, etc.).• I had the opportunity to have carried out clinical monitoring of global projects in different countries such as: Ecuador, Chile, Colombia, Guatemala, Mexico, Puerto Rico, USA.• I obtained a position in the Pharmacovigilance area thanks to my knowledge and skills within the Pharmacology area, working as Senior Drug Safety Associate, preparing the assigned tasks for global projects for 4 years, having an excellent performance and congratulations from my Country Manager and Project Directors of which I participatedAchievements:• I successfully managed more than 40 projects, adapting to the different demands and cultures of the clients, which made me reassign several projects in progress, humbly assuming their improvement.• I successfully managed an audit carried out by EMA, for a project completed a year ago. In which only the minimum observation of a missing Check-in a deliverables list was obtained, which was corrected without generating major incidents.• I won the international competition for a scholarship in the Master of Project Management carried out in 2013, obtaining recognition for the best thesis presented.

Customer served: Pfizer, Roche, Grunenthal, Genentech, AstraZeneca, Grupo TIMI, GlaxoSmithKline, Bayer, Celgene, Amgen, Genzyme.• Carry out the management of the projects assigned in the Start-Up Area.• Verify the quality control compliance of the assigned Projects with the preparation of respective reports on findings.• Prepare project management reports for clients, assigned monitors and Company personnelAchievements:• I managed to increase the number of research centers in a global project, in which 6 centers were allowed to be recruited and I managed to bring it to 33 centers, managing to incorporate these research centers, and receiving public congratulations from the Country Management for my management.• I proposed and managed the selection of new researchers to successfully complete the more than 10 assigned projects, establishing for this the filter of information crossing and endorsement of the sub researchers and the commitment of the monitors for their close follow-up, speeding up the investigations and making possible the management and approval of more research centers in each projec

Legal Representative:• Provide local legal endorsement to Foreign Clinical Research Organization CRA:• Coordinate with investigators (physicians), research nurses, study coordinators and/or site administrative staff for completion of required regulatory documents required for site IP approval (in coordination with the required parties: Regulatory Authority, Sponsor, etc).• Collaborate with investigators, research nurses and site staff to achieve issue resolution• Prepare, submit and/or assist sites with IEC/IRB submissions.• Update Regulatory document tracking in the SIPLAS RO database and provide organizational and administrative expertise.• Accountable for the review and transmission of regulatory documents in accordance with FDA, GCP, WPD and SOPs through site IP approval.• Coordinated 2 phase II-IV clinical trials in various Inmunology and System Nervous indications.