Frontend Code Evaluation Specialist In-Person English Trainer

Mercor Aula Intercultural; Quilmes; Remote; ARS 800,000 - 1,200,000; Full time

Benefits offered by this job

OSDE 310

Annual bonus

Inflation-based raises

21 vacation days

Remote work

Work flexibility

Job summary

Mercor Aula Intercultural in Buenos Aires, Argentina is seeking a pharmacovigilance specialist to review, assess, and process safety data across service lines. The role requires fluency in English, Spanish, and Italian and offers a 100% remote work arrangement.

Responsibilities include processing safety data, pharmacovigilance activities (AE collection, coding, narratives, literature tasks), and ensuring compliance with SOPs and project requirements.

Qualifications

• Bachelor's degree in Life sciences or related field (mandatory).
• Fluency in English and Italian (mandatory) - will be evaluated.
• Up to 3 years of clinical experience (desirable).
• 1 year pharmacovigilance experience valued (desirable).

Responsibilities

• Process safety data according to applicable regulations, guidelines, SOPs, and project requirements.
• Perform pharmacovigilance activities: collect and track adverse events, determine status, database entry, coding, narratives, and literature-related tasks.
• Ensure compliance with quality, productivity, and delivery standards per project requirements.
• Liaise with cross-functional teams and healthcare professionals to address project-related issues.

Skills

English

Spanish

Italian

Education

Bachelor's degree in Life sciences

Job description

Buenos Aires, Argentina
Full time
R

Job Overview

Review, assess, and process safety data and information across service lines, received from various sources. Distribute reports/data to both internal and external third parties following applicable regulations, Standard Operating Procedures (SOPs), and internal guidelines under the guidance and support of senior operation team members. This is a trilingual role requiring fluency in English, Spanish, and Italian.

Main Responsibilities

• Process safety data according to applicable regulations, guidelines, SOPs, and project requirements.
• Perform pharmacovigilance activities, including collecting and tracking incoming Adverse Events (AEs) and endpoint information, determining initial/update status of incoming events, database entry, coding AEs and products, writing narratives, and literature-related activities.
• Ensure compliance with quality, productivity, and delivery standards per project requirements.
• Liaise with different functional team members and healthcare professionals to address project-related issues.

Qualifications

• Bachelor's degree in Life sciences or a related field (mandatory)
• Fluency in English and Italian (mandatory) _(will be evaluated)_
• Up to 3 years of previous clinical experience (desirable)
• 1 year of pharmacovigilance experience will be highly valued (desirable)

What we offer to you

• OSDE 310
• Annual bonus by performance
• Salary adjustments during the year according to inflation rates.
• 21 vacations days
• Work flexibility
• 100% remote role!