Clinical Trial Assistant
hace 2 semanas
**Job Overview**Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.**Essential Functions**- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.- Assist the clinical team with 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 for completeness.- Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.- Assist with 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.- May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.**Qualifications**- Bachelor Degree in Pharmaceutical area or Life sciences.- 3 years administrative support experience or 1 year as a Study Coordinator.- Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.- Written and verbal communication skills including good command of English language.- Effective time management and organizational skills.- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.- Awareness of applicable clinical research regulatory requirements, i.e., 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.
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Clinical Trial Assistant
hace 2 semanas
Xico, México Icon A tiempo completoChina- ISS- Clinical Trial AssistantICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We are currently seeking a Clinical Trial Administrator to join...
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Clinical Trial Assistant
hace 2 semanas
Xico, México Pfizer A tiempo completoWhy Patients Need YouPfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes.Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary...
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Cta - Clinical Trial Assistant
hace 2 semanas
Xico, México Iqvia A tiempo completo**Job Overview**Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.**Essential Functions**- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining...
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Clinical Trial Associate
hace 2 semanas
Xico, México Pharm-Olam International A tiempo completoWhy Pharm-Olam:Pharm-Olam, LLC is a mid-size Contract Research Organization (CRO) that has a massive global reach.We are a company that strives to deliver cost-effective, quick-to-market clinical services in today's emerging marketplace.Pharm-Olam has one of the largest global footprints of any CRO today and we are committed to not only maintain our...
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Clinical Trial Manager: Lead Trial Design
hace 2 semanas
Xico, México Icon A tiempo completoA leading global healthcare organization is seeking a Clinical Trial Manager II to design and manage clinical trials, ensuring regulatory compliance and data analysis.The successful candidate will collaborate with cross-functional teams and has a Bachelor's degree with [X] years of experience in clinical trial management.The role offers a competitive salary...
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Clinical Trial Manager Ii
hace 2 semanas
Xico, México Icon A tiempo completoJR****** Clinical Trial ManagerICON plc is a world-leading healthcare intelligence and clinical research organization.We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We are currently seeking a Clinical Trial Manager II to join our...
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Senior Clinical Trial Manager — Remote
hace 2 semanas
Xico, México Icon A tiempo completoA leading healthcare organization is seeking a Senior Clinical Trial Manager for a remote role in Mexico.This position requires oversight of clinical trial budgets, effective study oversight, and mentoring of Clinical Research Associates.Candidates should have a strong background in clinical trial management, ideally with experience in therapeutic areas like...
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Senior Clinical Trial Manager
hace 2 semanas
Xico, México Icon Plc A tiempo completoSenior Clinical Trial ManagerICON plc is a world-leading healthcare intelligence and clinical research organization.We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentWe are currently seeking a Senior Clinical Trial Manager to join our...
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Clinical Trial Monitoring Manager
hace 2 semanas
Xico, México Msd A tiempo completoA leading pharmaceutical company in Veracruz, Mexico, seeks a Clinical Trial Manager to oversee a team of Clinical Research Associates (CRAs).The role involves managing site performance, ensuring regulatory compliance, and providing training and support to develop team talent.Ideal candidates will have experience in clinical trials and a strong background in...
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xico, México Iqvia Llc A tiempo completoA global clinical research organization is seeking a Clinical Trial Manager I in Mexico City. The successful candidate will ensure the clinical delivery of projects in compliance with regulatory requirements while managing recruitment targets and project risks. Applicants should possess a Bachelor's Degree and at least three years of clinical monitoring...
