8 publicaciones de empleo destacadas de data science en remoto argentina (¡Están contratando!)

CRA / Sr CRA
Thermo Fisher Scientific —Desde casa
- Tiempo completo
Lead Clinical Research Associate
PSI CRO —Desde casa
- Tiempo completo
Postulación rápida
Patient Engagement Lead (LATAM)
Precision for Medicine —Desde casa
Postulación rápida
Senior Manager, Security Architecture & Engineering
AspenView Technology Partners —Desde casa
- Por contrato
Postulación rápida
Senior Cloud Architect, Delivery (GenAI)
DoiT —Desde casa
Postulación rápida
Associate Project Manager - Language Services - Linguistic Validation
Thermo Fisher Scientific —Desde casa
- Tiempo completo
1d
Associate Project Manager - Language Services - Linguistic Validation
Thermo Fisher Scientific —Desde casa
- Tiempo completo
1d
Senior Medical Writer/Principal - Regulatory Documents
Syneos - Clinical and Corporate - Prod —Desde casa
- Tiempo completo
2d

More jobs to discover

Find similar jobs that you might be interested in.

Lead Clinical Research Associate
PSI CRO —Desde casa
Minimum of 5 years’ site monitoring experience with participation in global clinical projects as a Lead Monitor. Strong experience in Oncology preferred.
Postulación rápida

Quiero recibir la alerta de empleo más reciente para data science en remoto argentina

Al ingresar a tu cuenta, aceptas las Condiciones del servicio de SimplyHired y das tu consentimiento a nuestra Política de privacidad y Cookies.

Explorar empleos en más ubicaciones

data science jobs near remoto argentina

Empleos de Senior en Capital Federal, Buenos Aires

Empleos de Desarrollador Senior en Buenos Aires, Buenos Aires

Empleos de Patient Coordinator en Buenos Aires, Buenos Aires

Empleos de Customer Services en Aeropuerto Ezeiza, Buenos Aires

Empleos de Qa Lead en Buenos Aires, Buenos Aires

Empleos de Patient en Buenos Aires, Buenos Aires

Empleos de Senior Specialist en Buenos Aires, Buenos Aires

Empleos de Senior Support Analyst en Desde Casa

Empleos de Senior Creative Director en Capital Federal, Buenos Aires

Empleos de Jefe De Sistemas It Manager Salesforce en Provincia De Buenos Aires

Empleos de Key Account Manager en Buenos Aires, Buenos Aires

Empleos de Manager en Merlo, Buenos Aires

Empleos de Medical Writer en Buenos Aires, Buenos Aires

Empleos de Swiss Medical en Puerto Madero, Buenos Aires

Empleos de Swiss Medical en Lomas De Zamora, Buenos Aires

Empleos de Clinical Research en Buenos Aires, Buenos Aires

Empleos de Finance Associate en Buenos Aires, Buenos Aires

Empleos de Clinical Research Associate en Belgrano, Buenos Aires

Empleos de Clinical Research Associate en Buenos Aires, Buenos Aires

Empleos de Associate, Junior, Jr, Bootcamp en Belgrano, Buenos Aires

CRA / Sr CRA

Thermo Fisher Scientific -
Desde casa

Postulate ahora

Detalles del empleo

Tiempo completo

Descripción completa del empleo

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Clinical Research Associate (CRA / Sr. CRA)

At Thermo Fisher Scientific, our Clinical Research team supports leading pharmaceutical, biotechnology, and emerging biopharma companies in advancing innovative therapies worldwide. Having contributed to thousands of clinical trials across more than 100 countries, we are committed to accelerating research that improves patient lives.

As a Clinical Research Associate (CRA), you will play a key role in the monitoring and management of clinical trial sites, ensuring compliance with study protocols, ICH-GCP guidelines, regulatory requirements, and company procedures. Working closely with investigative sites and cross-functional teams, you will help safeguard patient safety, data integrity, and overall study quality while supporting the successful delivery of clinical research programs.

Position Summary

As a Clinical Research Associate (CRA), you will be responsible for performing and coordinating clinical monitoring and site management activities across clinical trials. You will conduct remote and on-site monitoring visits, ensure compliance with study protocols, ICH-GCP guidelines, applicable regulations, and SOPs, while safeguarding subject safety, data integrity, and audit readiness. You will collaborate closely with investigational sites, sponsors, and cross-functional project teams to support the successful execution of clinical studies.

Key Responsibilities:

Conduct on-site and remote monitoring visits using a risk-based monitoring approach.
Review source documentation, case report forms (CRFs), and study data to ensure accuracy, completeness, and compliance.
Perform site management activities, including site initiation, routine monitoring, and close-out visits.
Assess investigational product accountability through inventory and records review.
Identify site process issues, perform root cause analysis, and support implementation of corrective and preventive actions.
Ensure essential documents are maintained in accordance with ICH-GCP and regulatory requirements.
Prepare monitoring reports, follow-up letters, and study documentation within established timelines.
Maintain effective communication with investigational sites, sponsors, and internal study teams.
Support site identification, feasibility, and investigator engagement activities when applicable.
Track study progress and maintain accurate records in clinical trial management systems (CTMS) and other study tools.
Support regulatory inspections, audits, and quality initiatives.
Contribute to process improvements, project deliverables, and knowledge sharing across teams.

Minimum Qualifications:

Bachelor’s degree in Life Sciences, Nursing, or a related healthcare field, or an equivalent combination of education and experience.
Valid driver’s license, where applicable.
Ability to travel as required.

Experience:

Relevant clinical research and/or clinical monitoring experience in a pharmaceutical, biotechnology, CRO, or healthcare environment.
Candidates may be considered for CRA or Sr CRA opportunities based on their experience, qualifications, and demonstrated monitoring expertise.

Preferred Skills & Competencies:

Knowledge of ICH-GCP guidelines, clinical trial processes, and applicable regulations.
Understanding of medical terminology and therapeutic areas.
Strong critical thinking, problem-solving, and root cause analysis skills.
Experience with Risk-Based Monitoring (RBM) methodologies.
Excellent organizational and time management skills.
Strong written and verbal communication skills, including professional interaction with investigators and site personnel.
Ability to work independently and collaboratively in a global team environment.
Proficiency with Microsoft Office and clinical trial systems.
Strong attention to detail and commitment to quality.
English proficiency required.

Working Conditions and Environment

Work is performed in an office/ laboratory/clinical/and/or home office environment with exposure to electrical office equipment.
Frequent drives to site locations. Frequent travel, generally 60-80% but more for some individuals. May also include extended overnight stays.
Exposure to biological fluids with potential exposure to infectious organisms.
Personal protective equipment required such as protective eyewear, garments and gloves.
Exposure to fluctuating and/or extreme temperatures on rare occasions.

Postulate ahora

Refiná tu búsqueda

data science empleos en remoto argentina

Lead Clinical Research Associate

Patient Engagement Lead (LATAM)

Senior Manager, Security Architecture & Engineering

Senior Cloud Architect, Delivery (GenAI)

Associate Project Manager - Language Services - Linguistic Validation

Associate Project Manager - Language Services - Linguistic Validation

Senior Medical Writer/Principal - Regulatory Documents

More jobs to discover

Quiero recibir la alerta de empleo más reciente para data science en remoto argentina

Related Searches

Explorar empleos en más ubicaciones

Join Us as a Clinical Research Associate (CRA / Sr. CRA)

Position Summary

Key Responsibilities:

Conduct on-site and remote monitoring visits using a risk-based monitoring approach.

Review source documentation, case report forms (CRFs), and study data to ensure accuracy, completeness, and compliance.

Perform site management activities, including site initiation, routine monitoring, and close-out visits.

Assess investigational product accountability through inventory and records review.

Identify site process issues, perform root cause analysis, and support implementation of corrective and preventive actions.

Ensure essential documents are maintained in accordance with ICH-GCP and regulatory requirements.

Prepare monitoring reports, follow-up letters, and study documentation within established timelines.

Maintain effective communication with investigational sites, sponsors, and internal study teams.

Support site identification, feasibility, and investigator engagement activities when applicable.

Track study progress and maintain accurate records in clinical trial management systems (CTMS) and other study tools.

Support regulatory inspections, audits, and quality initiatives.

Contribute to process improvements, project deliverables, and knowledge sharing across teams.

Minimum Qualifications:

Bachelor’s degree in Life Sciences, Nursing, or a related healthcare field, or an equivalent combination of education and experience.

Valid driver’s license, where applicable.

Ability to travel as required.

Experience:

Relevant clinical research and/or clinical monitoring experience in a pharmaceutical, biotechnology, CRO, or healthcare environment.

Candidates may be considered for CRA or Sr CRA opportunities based on their experience, qualifications, and demonstrated monitoring expertise.

Preferred Skills & Competencies:

Knowledge of ICH-GCP guidelines, clinical trial processes, and applicable regulations.

Understanding of medical terminology and therapeutic areas.

Strong critical thinking, problem-solving, and root cause analysis skills.

Experience with Risk-Based Monitoring (RBM) methodologies.

Excellent organizational and time management skills.

Strong written and verbal communication skills, including professional interaction with investigators and site personnel.

Ability to work independently and collaboratively in a global team environment.

Proficiency with Microsoft Office and clinical trial systems.

Strong attention to detail and commitment to quality.

English proficiency required.

Working Conditions and Environment