Empleos actuales relacionados con Clinical Trial Assistant - Buenos Aires - IQVIA
-
Clinical Trials Assistant
hace 2 semanas
Buenos Aires, Argentina IQVIA A tiempo completo**_Although this role is home-based, it's a requirement to go to the client's office once a week, located in Belgrano, Buenos Aires._** 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...
-
Global Clinical Trials Assistant
hace 1 semana
Buenos Aires, Argentina IQVIA A tiempo completo**Join us as a **Clinical Trials Assistant!**: **What You´ll Do** 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...
-
Clinical Trials Assistant 1
hace 3 semanas
Buenos Aires, Argentina IQVIA LLC A tiempo completoClinical Trials Assistant 1 page is loaded## Clinical Trials Assistant 1locations: Buenos Aires, Argentinatime type: Full timeposted on: Posted Todayjob requisition id: R **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...
-
Regional Clinical Trial Manager
hace 3 semanas
Buenos Aires, Argentina ICON A tiempo completoRegional Clinical Trial Manager - Buenos Aires (FSP - Sponsor Dedicated) ICON 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...
-
Regional Clinical Trial Manager
hace 3 semanas
Buenos Aires, Argentina ICON A tiempo completoRegional Clinical Trial Manager - Buenos Aires (FSP - Sponsor Dedicated) ICON 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...
-
Clinical Trial Manager
hace 7 días
Buenos Aires, Argentina IQVIA LLC A tiempo completoClinical Trial Manager - Sponsor Dedicated page is loaded## Clinical Trial Manager - Sponsor Dedicatedlocations: Buenos Aires, Argentinatime type: Full timeposted on: Posted Todayjob requisition id: R **Clinical Trial Manager – Sponsor Dedicated.**Clinical Project Management services provide management of a clinical trial (s) in a local level....
-
Sponsor-Dedicated Clinical Trial Manager
hace 7 días
Buenos Aires, Argentina IQVIA LLC A tiempo completoA leading global provider of clinical research services is seeking a Clinical Trial Manager in Buenos Aires. You will manage end-to-end clinical trials, ensuring compliance with local regulations and sponsor SOPs. Key responsibilities include overseeing project management from start to finish, developing recruitment strategies, and maintaining communication...
-
Clinical Trial Manager
hace 4 semanas
Buenos Aires, Argentina IQVIA A tiempo completoBuenos Aires, Argentina | Full time | Home-based | R1519320 Clinical Trial Manager - Sponsor Dedicated.** Clinical Project Management services provide management of a clinical trial (s) in a local level. Services/deliverables include operational oversight of assigned project(s) at country level for end-to-end project management from start-up through to...
-
Trainee - Trial Capabilities
hace 3 semanas
Buenos Aires, Argentina Lilly A tiempo completoAt Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...
-
Sr. Associate-trial Capabilities Clinical
hace 2 semanas
Buenos Aires, Argentina Lilly A tiempo completoAt Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...
Clinical Trial Assistant
hace 3 semanas
**Join us as a **Clinical Trials Assistant**
**What You´ll Do**
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.
**What Will Help You Succeed**
- Graduated or currently pursuing a Bachelor´s Degree
- 1/2 years of administrative support experience or equivalent combination of education, training and experience.
- Knowledge of applicable clinical research regulatory requirement and clinical research terminology.
- 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.
**Unleash your potential to drive healthcare forward**
*Please submit your CV in English*
**#LI-Hybrid