10 publicaciones de empleo destacadas de customer experience associate en buenos aires, b (¡Están contratando!)

Senior CRA
IQVIA —Buenos Aires, Buenos Aires
- Tiempo completo
Senior - Consultoria Sap MM
PwC —Buenos Aires, Buenos Aires
- Tiempo completo
6d
Senior - SAP SD
PwC —Buenos Aires, Buenos Aires
- Tiempo completo
6d
Medical Director/Senior Medical Director Rheumatology (Client dedicated)
Thermo Fisher Scientific —Buenos Aires, Buenos Aires
- Tiempo completo
8d
Data Engineering III - Senior Associate
JPMorganChase —Buenos Aires, Buenos Aires
- Tiempo completo
Semi Senior - SAP MM
PwC —Buenos Aires, Buenos Aires
- Tiempo completo
10d
Semi Senior - Desarrollador BTP
PwC —Buenos Aires, Buenos Aires
- Tiempo completo
10d
Senior 2D/3D Animator
Monks —Buenos Aires, Buenos Aires
Postulación rápida
Assoc Dir, Epidemiology RWE
サイネオス・ヘルス —Buenos Aires, Buenos Aires
Senior - Consultor de Seguridad SAP
PwC —Buenos Aires, Buenos Aires
- Tiempo completo

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Senior - Consultoria Sap MM
PwC —Buenos Aires, Buenos Aires
Estudiante avanzado o graduado en Ingeniería, Sistemas, Administración o carreras afines. Más de 5 años de experiencia en SAP MM y/o EWM.
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Semi Senior - SAP MM
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Formación en carreras de sistemas, ingeniería o logística. Buscamos un/a Consultor/a SAP MM Junior / Semi Senior para sumarse a nuestro equipo de consultoría.
10d

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Senior CRA

IQVIA -
Buenos Aires, Buenos Aires

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Buenos Aires, Argentina | Full time | Home-based | R1523067

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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customer experience associate empleos en buenos aires, b

Senior CRA

Senior - Consultoria Sap MM

Senior - SAP SD

Medical Director/Senior Medical Director Rheumatology (Client dedicated)

Data Engineering III - Senior Associate

Semi Senior - SAP MM

Semi Senior - Desarrollador BTP

Senior 2D/3D Animator

Assoc Dir, Epidemiology RWE

Senior - Consultor de Seguridad SAP

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