Clinical Trials Assistant

hace 2 días


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 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**
- High School Diploma or equivalent
- Previous experience as clinical research assistant, study coordinator, clinical trial assistant.
- English Intermediate/Advanced.
- 3 years administrative support experience.
- Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
- 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.



  • Buenos Aires, Argentina IQVIA A tiempo completo

    A leading global provider of clinical research services is looking for a responsible research site assistant to provide critical support for clinical trials in Ciudad Autónoma de Buenos Aires. This part-time position will involve tasks such as data entry into electronic systems, maintaining study files, and scheduling patient visits. Candidates should have...


  • Buenos Aires, Argentina IQVIA LLC A tiempo completo

    Clinical 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...


  • Buenos Aires, Argentina IQVIA LLC A tiempo completo

    A leading global provider of clinical research services is seeking a Site Research Assistant in Ciudad Autónoma de Buenos Aires. This part-time role involves administrative tasks to support clinical trials, including data collection and regulatory compliance. Candidates should have a High School diploma, relevant experience, and good communication skills....


  • Buenos Aires, Argentina IQVIA LLC A tiempo completo

    A global provider of clinical research services is seeking a Clinical Trials Assistant in Buenos Aires. The role involves supporting Clinical Research Associates with document management, maintaining trial files, and ensuring compliance with regulations. Ideal candidates should have a High School diploma, along with 3 years of administrative support...


  • 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...


  • Buenos Aires, Argentina IQVIA A tiempo completo

    **Job Overview** Support Clinical Research Associates and Regulatory teams in administrative tasks to ensure accurate Trial Master File. **Key Responsibilities** - 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...


  • Buenos Aires, Argentina Parexel A tiempo completo

    Join Parexel’s team of changemakers as we help advance healthcare throughout the globe, all while keeping the patient at the heart of everything we do. **Job Title** Clinical Operations Specialist At Parexel, we are a leading Clinical Research Organization (CRO) company specializing in delivering life - changing medicines to patients. We are seeking...

  • Clinical Trial 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...


  • Buenos Aires, Argentina Milestone One A tiempo completo

    A global Site Enabling Organization is seeking a Clinical Trials Business Development Representative (Freelance) to support their Business Development team. The role involves building relationships with clients, promoting brand initiatives, and conducting client research. Candidates should have at least 4 years of experience in the clinical trials industry...


  • Buenos Aires, Argentina MSD A tiempo completo

    A global healthcare leader is seeking a Clinical Research Director in Buenos Aires, Argentina. This role is pivotal for leading clinical trial operations, ensuring compliance with international standards, and managing relationships with key stakeholders. The ideal candidate will possess a Bachelor’s degree in a scientific field with significant management...