Senior Geoquímico Minería – Proyectos Hidrogeológicos

Cashea

Quilmes

On-site

ARS 83,301,000 - 128,737,000

Full time

3 days ago
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Job summary

IQVIA in Buenos Aires, Argentina is seeking a full-time Clinical Research Associate (CRA). The role includes mentoring, quarterly reviews, and exposure to global projects with regional travel.

Responsibilities cover site initiation, monitoring and close-out visits, recruitment planning, protocol training, and data quality oversight. Strong English and 50% travel are required.

Training and development are provided to support career progression and performance recognition.

Qualifications

  • Bachelor's degree in a health care or other scientific discipline (or equivalent)
  • At least 2 years of remote monitoring experience or as Study Coordinator
  • Advanced English proficiency
  • 50% travel availability

Responsibilities

  • Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
  • Supporting the development of a subject recruitment plan
  • Establishing regular lines of communication plus administering protocol and related study training to assigned sites
  • Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
  • Managing progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolution

Skills

English (Advanced)

Education

Bachelor's degree in health care/science

Job description

Job Overview

Buenos Aires, Argentina Full time R Whether you’re beginning or continuing your career as a CRA, this role is an ideal stepping-stone. You’ll have training and development to plan and progress your career in the direction you choose. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards.

Award winning and innovative, we’ll give you access to cutting‑edge in‑house technology, allowing you to work on global projects but with a regional / home state travel remit, so no need for national travel in certain countries. You’ll be building a smart and flexible career with no limits.

Typical responsibilities
  • Performing site selection, initiation, monitoring and close‑out visits, plus maintaining appropriate documentation
  • Supporting the development of a subject recruitment plan
  • Establishing regular lines of communication plus administering protocol and related study training to assigned sites
  • Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
  • Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution

You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.

You should have
  • A Bachelor’s degree in a health care or other scientific discipline or educational equivalent
  • At least 2 years of remote monitoring experience or as Study Coordinator.
  • Advanced in English.
  • Travel availability (50%).
  • Alternatively, you should have an equivalent combination of education, training and experience.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. We are committed to integrity in our hiring process and maintain a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

EEO Minorities/Females/Protected Veterans/Disabled

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