Clinical Trial Assistant
hace 7 días
Job Purpose Asegúrese de que toda la información de su solicitud está actualizada y en orden antes de inscribirse en esta oportunidad. This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with Tigermed Jyton or sponsor Standard Operating Procedures (SOPs), International Conference on Harmonization Good Clinical Practice standard (GCP)， ISO14155 and other applicable regulations. The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget. Responsibilities 1. Study management and site management. Assist IRB submission to respective IRB Regulatory submission if needed. Perform pre-study visit to ensure eligible sites are selected according to site selection criteria/protocol, including but not limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study initiation and conduct in compliance with protocol and relevant regulations. Ensure Principal Investigator/study staff complies with safety reporting requirements, as defined in protocol, SOP and GCP. Track study recruitment to ensure recruitment target is achieved in all studies. Conduct monitoring visit according to monitoring plan and SOP; address issues with sites and complete monitoring visit report in a timely manner. Ensure timely coordination of study materials (medical device, IVD, drug, non-drug, equipment) to the site for start-up and throughout the study. 2. Training Provide ongoing training to site staff with regards to GCP, study protocol and requirements. Conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements. 3. Documentation Ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during and at study close-down. Maintain and update these documents in investigator site file and trial master file. Prepare/complete study records archiving according to protocol and sponsor requirements. 4. Safety Ensure safety information is disseminated to all sites according SOP and applicable regulations. Ensure SAE is reported within the timeline in compliance with SOPs and applicable regulations. 5. Finance and Administration ~ Finalize budget and obtain signed contract from site, prior to site initiation visit. 6. Ensure Study Payment Schedule is executed and retain relevant documents/receipts. ~ Study Tools and system Update and maintain Study tools/systems in a timely manner. Minimum Qualifications 1. Academic / Major: Bachelor degree in biomedical/medical science or equivalent (e.g. medical, Nurse, Pharmacology). 2. Professional Skills Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. xcskxlj 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills\Information-gathering skills Knowledge and/or experience in medical practice is a plus.
-
Clinical Trials Quality Assistant
hace 7 días
Valencia, España Health in Code Group A tiempo completoUna empresa líder en medicina personalizada busca un/a Clinical Trial Assistant en Valencia. El candidato/a dará soporte documental y administrativo en ensayos clínicos, garantizando el cumplimiento de normativas de calidad. Se requiere formación en Ciencias de la Salud, experiencia en entornos clínicos, y un nivel alto de inglés. Únete a un equipo...
-
Global Clinical Trial Assistant
hace 1 semana
Valencia, España Health in Code Group A tiempo completoEn Health in Code, grupo líder en medicina personalizada, nuestra misión es transformar la salud de las personas con enfermedades genéticas y sus familias. Lo hacemos ofreciendo soluciones basadas en datos genómicos que permiten decisiones clínicas más precisas y contribuyen a un sistema sanitario más eficiente, sostenible y centrado en el...
-
Clinical Trial Assistant
hace 2 semanas
Valencia, España Health in Code Group A tiempo completoEn Health in Code, grupo líder en medicina personalizada, nuestra misión es transformar la salud de las personas con enfermedades genéticas y sus familias. Lo hacemos ofreciendo soluciones basadas en datos genómicos que permiten decisiones clínicas más precisas y contribuyen a un sistema sanitario más eficiente, sostenible y centrado en el...
-
Clinical Trial Assistant
hace 1 semana
Valencia, España Health in Code Group A tiempo completoEn Health in Code, grupo líder en medicina personalizada, nuestra misión es transformar la salud de las personas con enfermedades genéticas y sus familias. Lo hacemos ofreciendo soluciones basadas en datos genómicos que permiten decisiones clínicas más precisas y contribuyen a un sistema sanitario más eficiente, sostenible y centrado en el...
-
Clinical Trial Assistant
hace 1 semana
Valencia, España Health in Code Group A tiempo completoEn Health in Code, grupo líder en medicina personalizada, nuestra misión es transformar la salud de las personas con enfermedades genéticas y sus familias. Lo hacemos ofreciendo soluciones basadas en datos genómicos que permiten decisiones clínicas más precisas y contribuyen a un sistema sanitario más eficiente, sostenible y centrado en el paciente....
-
Clinical Trial Assistant
hace 7 días
Valencia, España Health in Code Group A tiempo completoEn Health in Code, grupo líder en medicina personalizada, nuestra misión es transformar la salud de las personas con enfermedades genéticas y sus familias. Lo hacemos ofreciendo soluciones basadas en datos genómicos que permiten decisiones clínicas más precisas y contribuyen a un sistema sanitario más eficiente, sostenible y centrado en el paciente....
-
Clinical Research Assistant
hace 4 días
Valencia, España IQVIA A tiempo completoAre you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company that offers you an excellent benefits package and supports career progression whilst giving you the option of working flexibly? If so, come and join us - IQVIA are looking for a Clinical Research Assistant. This role, **with an immediate start for 6...
-
Valencia, España IQVIA A tiempo completoWe are looking for a **Psychologist/Psychiatrist to work as a Rater **to support the Clinical Trial team in conducting a clinical study in the field of Schizophrenia. This freelance role with flexible hours (5h per week) will support the site in Valencia. Start is immediate with a duration of 6 - 12 months. **Responsibilities will include**: - Attending,...
-
Valencia Area
hace 1 semana
Valencia, España IQVIA A tiempo completo**Valencia area** - **Onsite **Clinical Research Assistants / Clinical Trial Assistants - Part time contract (8h/week) for 12 weeks with IQVIA** Are you looking for your next opportunity in Clinical Research? Do you want to work for an industry leading company that offers you an excellent benefits package and supports career progression whilst giving you...
-
Head of Clinical Operations
hace 2 semanas
Valencia, España Barrington James A tiempo completoJob Title: Head of Clinical Operations¿Le interesa este puesto? Puede encontrar toda la información relevante en la descripción a continuación.Location: SpainReports To: Chief Operating Officer (COO) / Chief Executive Officer (CEO)About Us:Our partner is an innovative and rapidly growing Contract Research Organization (CRO) dedicated to providing...
