GLOBAL CTA MEDICAL AFFAIRS
Descripción de la oferta de empleo
Essential Functions • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.
., Trial Master File (TMF)) that track site compliance and performance within project timelines.
• Collaborate with clinical team on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
• Assist with periodic review of study files and completeness.
• Collaborate with CRAs and RSU on the preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
• Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
• Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
• Act as a mentor for less experienced Clinical Trial Assistants (CTAs).
• Assist with training and onboarding of new CTAs.
• May serve as subject matter expert for business processes.
• May lead CTA study teams.
• May assist with interviewing and screening of potential new team members • May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
• May participate in departmental quality or process improvement initiatives.
Qualifications • Bachelor Degree in Health or Science related field.
• 3+ years of clinical research experiences as a.
Clinical Trial Assistant or Study Coordinator.
• Experience in budgetary management.
• Excellent independent time management skills.
• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and Company Systems.
• Effective written and verbal communication skills including good command of English language.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
• Knowledge of applicable clinical research regulatory requirements, i.
., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
• Knowledge of applicable protocol requirements as provided in company training.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Learn more at https.
/\/jobs.
qvia.
om ","applicantLocationRequirements".
{"@type":"Country","name":"MX
Detalles de la oferta
- English
- En todo México
- Sin especificar - Sin especificar
- 21/11/2024
- 19/02/2025
That are in need of a physician to create the initial contact with the patients and construct their medical history over the phone... mx/ requisitos del puestowhat do you need? bachelors in: medicine (it's okay if you do not have your title yet, just a document to validate the career has been completed)abilities:......
Responsibilities: database management: manage and consolidate databases for our global it training program... content translation coordination: coordinate the translation of training content with trainers across global regions... we are currently looking for an administrative program & content manager......
Actividades recorridos en planta consulta de primer grado a trabajadores atención de emergencias coodinación del equipo de enfermería auditorias comedor y zonas comunes interesados postularse por este medio o acudir a los laboratorios de medical and health del bajio para una entrevista presencialrequisitos......
Conduct working sessions in large, global organisations to gather, understand and analyse business requirements for various functional areas, especially core hcm... we love when your pets visit us at the office! :) global perspective & people-centric approach great and dynamic work atmosphere......
Conduct working sessions in large, global organisations to gather, understand and analyse business requirements for various functional areas, especially core hcm... we love when your pets visit us at the office! :) global perspective & people-centric approach great and dynamic work atmosphere......
Oca global es el grupo internacional, líder en inspección, certificación, ensayos, consultoría y formación con más de 12 años de experiencia... si estas interesado en conocer mas sobre la posición, por favor adjunta tu cv, y nos pondremos en contacto contigo o bien acude a una entrevista física en nuestras......
Conduct working sessions in large, global organization to gather, understand, and analyze business requirements for various functional areas, especially core hcm... excellent communication, interpersonal, and consultative skills... this is an exciting opportunity to be at the forefront of the transformation......
Private medical work location: mexico... requisitos del puesto qualifications & professional skills last year students/bachelor’s degree (or higher) with a focus in technology... knowledge in data analytics/big data... as a workday integration consultant you will drive clients on their digital transformation......
Conduct working sessions in large, global organization to gather, understand, and analyze business requirements for various functional areas, especially core hcm... otros datos del puestoegresados de carreras como ingeniería industrial, mecatrónica, o cualquier ingeniería aplican a esta posición, así......
Hoy somos líderes en entretenimiento a nivel global gracias a nuestra excelencia en servicio y el talento de nuestros colaboradores... vivir a no más de 30 minutos del cine... iluminar la película de tu vida en la empresa más importante de entretenimiento... requisitos del puestoque necesitas: indispensable......
