Clinical Research Associate II (San Miguel de Tucumán)
Clinical Research Associate II (San Miguel de Tucumán)
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San Miguel de Tucumán, Argentina
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Publicado: hace menos de una semana
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Descripción
Clinical Research Associate II (FSP
- Sponsor dedicated)
What You Will Do You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Key Responsibilities
- 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 2 years of experience as a Clinical Research Associate.
- Advanced English level.
- 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.
- Willingness to travel as required (approximately 60%).
What ICON Can Offer You Our benefits are designed to be competitive within each country and are focused on well‑being and work‑life balance opportunities for you and your family.
Our Benefits Examples Include
- Various annual leave entitlements.
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a general network of over 80,000 independent specialized professionals who are there to support you and your family’s well‑being.
- Life a Postúlate en Kit Empleo: kitempleo.com.ar/empleo/qasr7
- Sponsor dedicated)
What You Will Do You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Key Responsibilities
- 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 2 years of experience as a Clinical Research Associate.
- Advanced English level.
- 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.
- Willingness to travel as required (approximately 60%).
What ICON Can Offer You Our benefits are designed to be competitive within each country and are focused on well‑being and work‑life balance opportunities for you and your family.
Our Benefits Examples Include
- Various annual leave entitlements.
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a general network of over 80,000 independent specialized professionals who are there to support you and your family’s well‑being.
- Life a Postúlate en Kit Empleo: kitempleo.com.ar/empleo/qasr7
Información clave
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Nombre de la empresaIcon Strategic Solutions
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Nombre de la vacanteClinical Research Associate II (San Miguel de Tucumán)
Consejos de seguridad
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Más info sobre el aviso
El aviso Clinical Research Associate II (San Miguel de Tucumán) fue publicado en la categoría San Miguel de Tucumán Otras ofertas de empleo de Locanto.
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