START Center for Cancer Research (“START”) es la mayor red mundial de centros de fase I, dedicada por completo a la investigación clínica oncológica. A lo largo de nuestra historia, START ha proporcionado esperanza a pac…
Asistente Administrativo Clínico / Secretario/a de Unidad
Logroño, Rioja, Spain · On-site
Mid level
START Center for Cancer Research (“START”) es la mayor red mundial de centros de fase I, dedicada por completo a la investigación clínica oncológica. A lo largo de nuestra historia, START ha proporcionado esperanza a pac…
Skills: Administrative Support, English B2, Microsoft Office, Data Protection, Customer Service
The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global …
Skills: Regulatory Submissions, IRB Coordination, FDA Compliance, IBC Submissions, Investigator Site File Maintenance
START Center for Cancer Research (“START”) es la mayor red mundial de centros de fase I, dedicada por completo a la investigación clínica oncológica. A lo largo de nuestra historia, START ha proporcionado esperanza a pac…
The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global …
Skills: Clinical Research Coordination, Oncology Clinical Trials, Good Clinical Practice (GCP), Patient Screening, Informed Consent Process
The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global …
Skills: Patient Assessment, Telephone Triage, Patient Education, Electronic Medical Records (EMR), ECG Performance
The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global …
Skills: Clinical Research Coordination, Oncology Clinical Trials, Good Clinical Practice (GCP), Patient Screening, Informed Consent Process
The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global …
Skills: Clinical Research Coordination, Oncology Clinical Trials, Good Clinical Practice (GCP), Patient Screening, Informed Consent Process
The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. To date, over 45 therapies conducted at START locations have obtained FDA/EMA…
Skills: Chemotherapy Administration, Immunotherapy Administration, Venipuncture, IV Insertion, Central Line Management
Técnico/a de Farmacia – Área Hospitalaria / Investigación Clínica
Logroño, Rioja, Spain · On-site
Entry level
Acerca del empleo START Center for Cancer Research (“START”) START es una empresa líder en ensayos clínicos en fase I especializada en oncología. Nuestra misión es acelerar el desarrollo de nuevos tratamientos contra el …
Los Angeles, California, United States · Remote OK
$25/hr–$35/hr
Mid level
The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global …
Skills: Clinical Data Entry, Case Report Forms (CRFs), Query Resolution, Medical Terminology, Office Administration
The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. To date, over 45 therapies conducted at START locations have obtained FDA/EMA…
Skills: Clinical Research Coordination, Patient Screening, Informed Consent Process, Data Collection, GCP Compliance
The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global …
Skills: Biospecimen Processing, Sample Handling, GLP Compliance, Medical Terminology, Microsoft Office
The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global …
Skills: Medication Order Verification, Investigational Drug Dispensing, Sterile Compounding, Patient Counseling, Drug Accountability
The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global …
East Brunswick Township, New Jersey, United States · On-site
Mid level
The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global …
Skills: Clinical Research Coordination, Oncology Clinical Trials, Good Clinical Practice (GCP), Patient Screening, Informed Consent Process
The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global …
Skills: Clinical Research Coordination, Oncology Clinical Trials, Good Clinical Practice (GCP), Patient Screening, Informed Consent Process
The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. To date, over 45 therapies conducted at START locations have obtained FDA/EMA…
The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global …
Se valorará formación específica en investigación clínica (CTA, GCP u otros cursos relacionados)START Center for Cancer Research (“START”) es la mayor red mundial de centros de fase I, dedicada por completo a la investig…
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Full-time
bachelor degree, postgraduate degree
Permanent Full-Time Contract, Participation in Innovative High-Impact Studies, International and Collaborative Environment, Continuous Professional Development, Access to Cutting-Edge Research Projects, Attendance at International Congresses
Posted 2d ago
~38 hrs/week
Spanish
Responsibilities
Lead and supervise sponsored oncology clinical trials, ensuring strict adherence to study protocols and ICH-GCP guidelines. Manage the integral execution of studies, focusing on patient safety, data quality, and collaboration with sponsors and regulatory authorities.
Requirements
Requires a Medical Degree with a specialty in Oncology and solid knowledge of ICH-GCP and regulatory standards. High professional English proficiency and the ability to manage multiple studies and multidisciplinary teams are essential.
Full job description
START Center for Cancer Research (“START”) es la mayor red mundial de centros de fase I, dedicada por completo a la investigación clínica oncológica. A lo largo de nuestra historia, START ha proporcionado esperanza a pacientes con cáncer en consultas de comunidades globales, ofreciéndoles acceso a ensayos de vanguardia en Estados Unidos y Europa. En la actualidad, con más de 1.300 estudios realizados y con centros de investigación en Estados Unidos y en España, Portugal e Irlanda, la misión de START es acelerar el desarrollo de nuevos medicamentos contra el cáncer que mejoren la calidad de vida y la supervivencia de los pacientes con cáncer y conduzcan a su eventual curación. Hasta la fecha, más de 43 terapias realizadas en centros START han obtenido la aprobación de la FDA/EMA
Vacante Disponible: Investigador/a Clínico/a
Sobre la posición
Buscamos un/a Investigador/a Clínico/a, médico/a con experiencia en investigación clínica, para liderar y supervisar ensayos clínicos patrocinados, garantizando el cumplimiento de los protocolos de estudio, las directrices ICH-GCP y la normativa aplicable.
La persona seleccionada será responsable de la gestión integral de estudios clínicos, velando por la seguridad de los pacientes, la calidad de los datos y la correcta ejecución de los ensayos, en estrecha colaboración con patrocinadores, monitores y equipos multidisciplinares.
Funciones principales
Liderar la ejecución de ensayos clínicos como Investigador/a
Garantizar el cumplimiento de los protocolos del estudio, las normas ICH-GCP y los requisitos regulatorios vigentes.
Proteger los derechos, la seguridad y el bienestar de los pacientes participantes.
Obtener y documentar correctamente el consentimiento informado.
Supervisar la preparación y administración de medicamentos en investigación.
Realizar visitas clínicas de acuerdo con el protocolo del estudio.
Registrar visitas, acontecimientos adversos y documentación clínica en los sistemas electrónicos correspondientes.
Notificar acontecimientos adversos graves (SAEs) dentro de los plazos establecidos.
Evaluar la viabilidad de nuevos estudios clínicos y participar en reuniones de revisión de protocolos.
Asistir a reuniones de investigadores, visitas de inicio, monitorización y cierre de estudios.
Colaborar con monitores (Clinical Research Associates), patrocinadores y autoridades regulatorias durante auditorías e inspecciones.
Participar activamente en reuniones de investigación clínica de Fase I y en iniciativas de mejora continua.
Requisitos
Licenciatura o Grado en Medicina con especialidad en Oncología
Conocimiento sólido de las normas ICH-GCP (Good Clinical Practice) y normativa regulatoria aplicable.
Capacidad para gestionar múltiples estudios y coordinar equipos multidisciplinares.
Excelentes habilidades de comunicación
Nivel alto de inglés profesional, tanto escrito como hablado.
Alto sentido de la responsabilidad, ética profesional y orientación a la calidad.
Valoraremos especialmente
Experiencia previa en ensayos clínicos, especialmente en estudios de Fase I
Experiencia en auditorías e inspecciones regulatorias.
Conocimientos de sistemas electrónicos de gestión de datos clínicos e historias clínicas electrónicas.
¿Qué ofrecemos?
Incorporación a una organización líder en investigación clínica.
Contrato permanente a tiempo completo - 37.5 horas de lunes a viernes.
Participación en estudios innovadores y de alto impacto científico.
Entorno internacional y colaborativo.
Desarrollo profesional continuo y acceso a proyectos punteros en investigación.
Asistencia a congresos internacionales.
Posibilidad de expansión académica - PhD
Clinical Trials Workshop AACR/ESMO
Related keywords
OncologyClinical TrialsPhase IICH-GCPFDAEMAClinical Research AssociateSAEPatient SafetyMedical DegreeRegulatory AuditsElectronic Data CaptureElectronic Health RecordsCancer Research
Deeply rooted in community oncology centers globally, the START Center for Cancer Research ("START") provides patients with access to specialized Phase 1 clinical trials for novel anti-cancer agents. With research sites in the United States and in Spain, Portugal, and Ireland, START’s clinical trial sites have conducted more than 1,500 early phase clinical trials, including for 50 therapies that have gained FDA/EMA approval. Founded in Texas in 2007, START today boasts 40+ Principal Investigators (PIs) across its worldwide clinical trial sites. With over 100,000+ square feet of world-class research facilities, START offers patients comprehensive treatment plans that include multi-specialty services, genetic profiling of tumors, targeted therapies, state-of-the-art treatment technology, and advanced access to clinical research options. START is committed to accelerating passage from trials to treatments, and to delivering hope to patients, families, and physicians around the world.
Offices: 4383 Medical Dr, San Antonio, Texas 78229, US · 5800 Foremost Dr SE, Grand Rapids, Michigan 49546, US · 2965 W 3500 S, #4th, West Valley City, Utah 84119, US · C. de Oña, 10, Madrid, 28050, ES · 823 82nd Pkwy, Suite B, Myrtle Beach, South Carolina 29572, US
Deeply rooted in community oncology centers globally, the START Center for Cancer Research ("START") provides patients with access to specialized Phase 1 clinical trials for novel anti-cancer agents. With research sites in the United States and in Spain, Portugal, and Ireland, START’s clinical trial sites have conducted more than 1,500 early phase clinical trials, including for 50 therapies that have gained FDA/EMA approval. Founded in Texas in 2007, START today boasts 40+ Principal Investigators (PIs) across its worldwide clinical trial sites. With over 100,000+ square feet of world-class research facilities, START offers patients comprehensive treatment plans that include multi-specialty services, genetic profiling of tumors, targeted therapies, state-of-the-art treatment technology, and advanced access to clinical research options. START is committed to accelerating passage from trials to treatments, and to delivering hope to patients, families, and physicians around the world.
Offices: 4383 Medical Dr, San Antonio, Texas 78229, US · 5800 Foremost Dr SE, Grand Rapids, Michigan 49546, US · 2965 W 3500 S, #4th, West Valley City, Utah 84119, US · C. de Oña, 10, Madrid, 28050, ES · 823 82nd Pkwy, Suite B, Myrtle Beach, South Carolina 29572, US