Ejecutivo/A Senior De Tesorería E Inversiones

Consejo Profesional de Ciencias Económicas de la Ciudad Autónoma de Buenos Aires; Buenos Aires; On-site; ARS 1,800,000 - 2,700,000; Full time

Job summary

The Senior Clinical Research Associate role based in Buenos Aires is pivotal to planning, execution, and oversight of clinical trials. You will ensure data integrity, comply with GCP/ICH guidelines, and support project teams across sites.

Requirements include a health science Bachelor’s degree, at least four years of on-site monitoring experience, advanced English, and strong organizational and communication skills to manage regulatory submissions and CTMS/EDC systems.

Qualifications

• Bachelor’s degree in health care or a scientific field.
• At least 4 years of on-site monitoring experience.
• Advanced English proficiency.
• In-depth knowledge of GCP/ICH guidelines and regulatory requirements.

Responsibilities

• Perform site selection, initiation, monitoring and close-out visits with proper documentation.
• Support the development of a subject recruitment plan.
• Maintain protocol training and communicate with assigned sites.

Skills

English (Advanced)

GCP/ICH knowledge

Regulatory compliance

CTMS

EDC

On-site monitoring

Communication skills

Organizational skills

Teamwork

Independent work

Education

Bachelor's degree in health care or science

Tools

CTMS

EDC

Job description

Senior Clinical Research Associate

Buenos Aires, Argentina
Full time
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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.
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