ACUTA
Providing Regulatory Information Management (RIM) solutions and services to the Life Sciences and related industry.
- Open roles
- 40
- New role every
- ~0.1 days
Company signals
Score: 69Job facts
- Location
- Mexico City, Mexico
- Type
- Full-time
- Posted
- Jun 18, 2026
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MI Ops Specialist 1
at ACUTA
100% remote role
Job Overview
TheMedical Information Case Processor responsibilities include receiving and documenting incoming telephone calls or emails from investigative sites or other sources reporting Lifecycle Safety Data.
This is a trilingual role requiring fluency in English, Spanish, and French.
Responsibilities include:
• Medical Information Case processor responsibilities include receiving and
documenting incoming calls, chats, and emails from external customers such as
patients and/or healthcare providers) and responding to their enquiries about
products. Summarizing these reports based on information identified as vital
to the project
• Disseminate clear, accurate information to healthcare professionals and
patients based on the approved call scripts and/or other approved resources
related to the use of client products
• Creating Adverse Event and Product Quality Complaint reports requiring
concise data entry covering everything from patient symptoms, admission and
results – this will include medical terminology, writing narratives,
generating case queries.
• Clarify, investigate and capture adverse event and product quality
information
Essential Functions
• Process Safety data according to applicable regulations, guidelines,
Standard Operating procedures (SOPs) and project requirements.
• To perform Pharmacovigilance activities per project requirement including
but not limited to, collecting and tracking incoming - Adverse
Events(AE)/endpoint information
• Ensure to meet quality standards per project requirements.
• To demonstrate problem solving capabilities.
Qualifications
-
Bachelor’s degree in Life sciences or a related field (mandatory)
-
Fluency in English and French (mandatory) We 're considering B2 level in third language as long as you can reach a C1 minimum in English! (will be evaluated)
-
Up to 3 years of previous clinical experience (desirable)
-
1 year of pharmacovigilance experience will be highly valued (desirable)
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
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.