Site Research Assistant in Córdoba Argentina

hace 4 meses


Buenos Aires, Argentina IQVIA A tiempo completo

Job Overview
Perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies.

Essential Functions
- Provide clinical research support to investigators and site staff, including
- Verify and/or correct research study information on source documents; research queries and variances; and provide

feedback to the site data collector.
- Input research study data into trial Electronic Data Capture (EDC) system, maintaining quality control for content,

accuracy, and completeness.
- Prepare and maintain research study files. Compile, collate and submit study information within established deadlines.
- Collect and submit regulatory/ethics documentation pertaining to the research study.
- Maintain the FDA 1572 form for assigned research studies.
- Input visit data into clinical trial management system (CTMS) to track patient visits and procedures completed against the study budget.

**Qualifications**:

- High School Diploma or equivalent High School Diploma Req
- Educational equivalent and 2 years’ relevant work experience in a clinical environment or medical setting; or equivalent combination of education, training and experience Req
- Basic knowledge of clinical trials
- In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study

schedules
- Basic knowledge of medical terminology
- Excellent interpersonal skills
- Ability to pay close attention to detail
- Ability to establish and maintain effective working relationships with coworkers, managers and clients
- Applicable certifications and licenses as required by the company, country, state, and/or other regulatory bodies Upon Hire Req



  • Buenos Aires, Argentina IQVIA A tiempo completo

    **Great opportunity if you want to join one of the greatest CROs and start your journey!** **Job Overview** Perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies. **Essential Functions** - Provide...


  • Buenos Aires, Argentina Novasyte A tiempo completo

    Great opportunity if you want to join one of the greatest CROs and start your journey! - Job Overview - Perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies.- Essential Functions- Provide clinical research...


  • Buenos Aires, Argentina Novasyte A tiempo completo

    Job Overview Perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies. Essential Functions - Provide clinical research support to investigators and site staff, including - Verify and/or correct research...


  • Buenos Aires, Argentina IQVIA A tiempo completo

    **Great opportunity if you want to join one of the greatest CROs and start your journey!** **Job Overview** Perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies. **Essential Functions** - Provide...


  • Buenos Aires, Argentina IQVIA A tiempo completo

    **Great opportunity if you want to join one of the greatest CROs and start your journey!** **Job Overview** Perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies. **Essential Functions** - Provide...


  • Buenos Aires, Argentina Novasyte A tiempo completo

    Great opportunity if you want to join one of the greatest CROs and start your journey! Job Overview Perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies. Essential Functions - Provide clinical research...


  • Buenos Aires, Argentina IQVIA A tiempo completo

    **Great opportunity if you want to join one of the greatest CROs and start your journey!** **Job Overview** Perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies. **Essential Functions** - Provide...


  • Buenos Aires, Argentina Novasyte A tiempo completo

    Great opportunity if you want to join one of the greatest CROs and start your journey! Job Overview Perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies. Essential Functions - Provide clinical research...


  • Buenos Aires, Argentina IQVIA A tiempo completo

    **Great opportunity if you want to join one of the greatest CROs!** **Job Overview** Perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies. **Essential Functions** - Provide clinical research support to...


  • Buenos Aires, Argentina Novasyte A tiempo completo

    Great opportunity if you want to join one of the greatest CROs! Job Overview Perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies. Essential Functions - Provide clinical research support to...


  • Buenos Aires, Argentina IQVIA A tiempo completo

    **Great opportunity if you want to join one of the greatest CROs and start your journey!** **Job Overview** Perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies. **Essential Functions** - Provide...


  • Buenos Aires, Argentina IQVIA A tiempo completo

    **Job Overview (Part-Time, Fixed-Term Role)** Perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures **at a field-based clinical site** to collect data on patients enrolled and/or seeking enrollment in clinical studies. **Essential Functions** - Provide clinical research support to...


  • Buenos Aires, Argentina PSI A tiempo completo

    Job SummaryPSI is seeking a highly skilled Clinical Research Site Manager to join our international team. As a key support to clinical research projects, you will be responsible for streamlining communication, maintaining systems, and managing documents and information.Key ResponsibilitiesAct as the primary point of contact between site personnel and CRA...

  • Legal Assistant

    hace 3 meses


    Buenos Aires, Argentina Medpace, Inc. A tiempo completo

    Job Summary: Join Medpace at our CABA office! Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Legal Assistant to join our LatAm Site Contract Team within the Clinical Operations team. This position will report to the LatAm Senior Contract Manager and will play a key role in the study start-up and clinical...


  • Buenos Aires, Argentina IQVIA Argentina A tiempo completo

    Job OverviewWe are seeking a highly skilled Clinical Research Associate to join our team at IQVIA Argentina. As a Clinical Research Associate, you will be responsible for ensuring the quality and integrity of study site practices related to the proper conduct of clinical trials.Key ResponsibilitiesSite MonitoringPerform site monitoring visits to ensure...


  • Buenos Aires, Argentina Novasyte A tiempo completo

    The Sr. Site Activation Specialist will perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Developing professional...


  • Buenos Aires, Argentina MSD A tiempo completo

    Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team at MSD. As a Clinical Research Associate, you will be responsible for ensuring the smooth conduct of clinical trials at assigned sites, ensuring compliance with regulatory requirements, and maintaining strong relationships with site staff.Key ResponsibilitiesDevelop and...


  • Buenos Aires, Argentina MSD A tiempo completo

    Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team at MSD. As a Clinical Research Associate, you will be responsible for ensuring the successful conduct of clinical trials in accordance with Good Clinical Practice (GCP) and regulatory requirements.Key ResponsibilitiesSite ManagementDevelop and maintain strong...


  • Buenos Aires, Argentina IQVIA A tiempo completo

    **Great opportunity if you want to join one of the greatest CROs and start your journey!** **Job Overview** Perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies. **Essential Functions** - Provide...

  • Medical Monitor

    hace 2 meses


    Buenos Aires, Argentina Innovaderm Research A tiempo completo

    The Medical Monitor provides medical and scientific support to clinical research programs. The Medical Monitor will perform thorough data review to ensure data integrity and subject safety oversight, and will communicate with sites, investigators, and internal project team members to ensure questions are promptly addressed.This role will be perfect for you...