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

Clinial Research Associate I
ICON Plc —Buenos Aires, Buenos Aires
- Tiempo completo
2d
Principal Auditor, QA *GCP Exp Required
Syneos - Clinical and Corporate - Prod —Buenos Aires, Buenos Aires
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Syneos Health Commercial Solutions —Buenos Aires, Buenos Aires
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Wyndham Hotels & Resorts —Buenos Aires, Buenos Aires
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EY —Capital Federal, Buenos Aires
1d
Senior Manager, Project Controls
Worley —Buenos Aires, Buenos Aires
Technical Lead - Java
dLocal —Buenos Aires, Buenos Aires
- Tiempo completo
Postulación rápida
4d
Sr. CRA (Unblinded)
ICON Plc —Buenos Aires, Buenos Aires
- Tiempo completo
5d
CRA II / Senior CRA
ICON Plc —Buenos Aires, Buenos Aires
- Tiempo completo
2d
Senior Salesforce Developer
Launchpad Technologies —Capital Federal, Buenos Aires
Postulación rápida
Manager, Commercial Performance & Planning
The Walt Disney Company (LATAM) —Buenos Aires, Buenos Aires
2d
Lead C# Software Architect
Marvik —Buenos Aires, Buenos Aires

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Principal Auditor, QA *GCP Exp Required
Syneos - Clinical and Corporate - Prod —Buenos Aires, Buenos Aires
A minimum 5 years experience within GCP (Phase I-IV Clinical Trials) required. Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs,…
11d

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Clinial Research Associate I

ICON Plc -
Buenos Aires, Buenos Aires

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Detalles del empleo

Tiempo completo
Hace 2 días

Descripción completa del empleo

Clinial Research Associate I

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.

As a CRA I at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programmes.

What You Will Do:

Your role will involve delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.
Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements.

Your Profile:

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

Required qualifications and experience:

University degree in medicine, science, or equivalent
Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
Excellent written and verbal communication in English
Good social skills enabling you to deal with queries in a timely manner
Willingness to travel as required (approximately 35%)

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

Clinial Research Associate I

Principal Auditor, QA *GCP Exp Required

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