Remote Jobs Buenos Aires, Argentina ∙ Hiring now - Page 3

Logo

Coursera

Learn skills from top universities online. Advance your career today!

Sponsored by Coursera

Logo

Oyster

Hire globally with Oyster. Simplify payroll and compliance.

Sponsored by Oyster

Logo

Exponent

Ace your tech interviews with mock sessions and expert coaches from top companies.

Sponsored by Exponent

IQVIA Logo

Hybrid CRA1

IQVIA · Buenos Aires, Argentina, Argentina · Hybrid

Previous Next

Hybrid Senior CRA

IQVIA · Buenos Aires, Argentina, Argentina · Hybrid

Apply Now Logo

Blinkist – Key book insights in 15 minutes. Save 40% now!

Sponsored by Blinkist

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