Global CTA

Global CTA

01 jun
|
Importante empresa del sector
|
Buenos Aires

01 jun

Importante empresa del sector

Buenos Aires

Buenos Aires, Buenos Aires



IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.



PURPOSE



Provide administrative support to clinical projects under direction of line manager and/or other designated clinical team members. Assists with general administrative functions as required.



RESPONSIBILITIES



- Assist Clinical Research Associates (CRAs)/In-house Clinical Research Associate (iCRA)





and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.

- Assist the clinical team in 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/iCRAs 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 and with required approval.

- May perform assigned administrative tasks to support team members with clinical trial execution.



All responsibilities are essential to job functions unless noted as non-essential (N).



REQUIRED KNOWLEDGE, SKILLS AND ABILITIES



- Awareness of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

- Basic knowledge of applicable protocol requirements as provided in company training

- Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint

- Good 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



MINIMUM REQUIRED EDUCATION AND EXPERIENCE



- High or Secondary School diploma/certificate or country’s educational equivalent and 2 years administrative support experience; or equivalent combination of education, training and experience

- Advance English Language is required.



Join Us



Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.



Forge a career with greater purpose, make an impact, and never stop learning.

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