Senior CRA

IQVIA • English: C1 • Clinical Research • Data & Analytics • Travel required • Bachelor's Degree • 8 months ago
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Salary
≈ $46k – $106k per year (Estimated)
Location
In office (Buenos Aires)
Seniority
Senior · 4+ years exp
Employment
Full-Time
Overview
Company
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IQVIA

IQVIA is an American company formed in 2016 by the merger of the contract research organisation Quintiles, founded in 1982, with the pharmaceutical data business IMS Health. It runs clinical trials on behalf of drug and device makers and simultaneously operates one of the largest healthcare data estates in the world, covering prescriptions, claims and electronic medical records, which it sells back to the same industry for commercial planning and real-world evidence studies. Headquartered in Durham, North Carolina and listed on the New York Stock Exchange, it employs close to ninety thousand people and combines the trial and data businesses in what it calls connected intelligence.
iqvia.com • HQ: Durham, United States • Data Quality • Data & Analytics • Health Care • Clinical Research • 5000+ employees • Est. 1982

The Senior Clinical Research Associate (CRA) will play a crucial role in the planning, execution, and management of clinical trials. This position requires a highly skilled and experienced professional who can ensure the integrity of clinical data, compliance with regulatory requirements, and the overall success of clinical research projects.

While projects vary, your typical responsibilities might include:

  • 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.

REQUIREMENTS

You should have:

  • A Bachelor's degree in a health care or other scientific discipline or educational equivalent
  • At least 4 years of on-site monitoring experience.
  • Advanced in English.
  • In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
  • Strong organizational and time management skills.
  • Excellent communication and interpersonal skills.
  • Ability to work independently and as part of a team.
  • Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
  • Willingness to travel as required.

If you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to apply now and join our team.

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. Learn more at https://jobs.iqvia.com

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