20 publicaciones de empleo destacadas de staff data en b (¡Están contratando!)

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Disney Entertainment and ESPN Product & Technology —Buenos Aires, Buenos Aires
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Sr. CRA (Unblinded)
ICON Plc —Buenos Aires, Buenos Aires
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CRA II (Sponsor Dedicated)

ICON Plc -
Buenos Aires, Buenos Aires

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Detalles del empleo

Tiempo completo

Descripción completa del empleo

CRA II - Argentina

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

The CRA II plays a key role in ensuring data integrity, patient safety, and overall quality of clinical trials conducted at investigative sites. The CRA II monitors trials either onsite or remotely, ensuring compliance with protocols, ICH-GCP guidelines, ICON and/or customer SOPs, and applicable regulatory requirements. This role offers hands-on experience with increasingly complex studies and support from project teams and leadership. The CRA II is always accountable for inspection readiness of their sites.

What You Will Do:

Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
Collaborating with investigators and site staff to facilitate smooth study conduct.
Performing data review and resolution of queries to maintain high-quality clinical data.
Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Your Profile:

You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.

Required qualifications and experience:

Bachelor's degree in a scientific or healthcare-related field.
Minimum of 1.5 years of experience as a Clinical Research Associate.
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
Strong organizational and communication skills, with attention to detail.
Ability to work independently and collaboratively in a fast-paced environment.

#LI-FP1

#LI-Remote

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request .

Are you a current ICON Employee?

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staff data empleos en b

CRA II (Sponsor Dedicated)

Sr Clinical Project Manager

CRA 2, Argentina

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Sr. CRA (Unblinded)

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Senior Clinical Research Associate (level dependent on experience)

Senior Manager, Project Controls

Regional Clinical Trial Manager

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