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
- Buenos Aires, Argentina
- Type
- Full-time
- Posted
- May 26, 2026
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Neurologist - Medical Data Review Manager
at ACUTA
Job Overview
Review structured clinical patient data output without direct access to
medical charts to ensure medical plausibility and determine adherence to
protocol and overall completeness and readiness of the supplied patient
information for next level of review.
Essential Functions
• Identify any anomalies in patient reported data that require further
investigation with the clinical site to determine overall accuracy
• Review all inclusion and exclusion criteria to ensure each patient meets
minimum level of acceptance into the clinical trial
• Review investigation product dosing records to determine adherence to
protocol and identify possible inaccurate / missed dosages
• Review all reported Adverse Events (AEs) , Concomitant Medication and
medical history information to ensure all supporting information is expected
and/or implausible data is verified and adherence to protocol expectations and
its impact on other patient reported/observed information (e.g., laboratory
results, AEs, etc.)
• Ensure end-of-treatment (EOT) and end-of-study (EOS) information is
correctly documented to determine primary reason for the patient ending
treatment or ending participation in the clinical trial
• Review all laboratory results to ensure completeness of information and
adherence to protocol schedule of events and determine if reported laboratory
values represent a potential safety condition not reported in the AE
information for the patient
• Review any other information as necessary to determine overall readiness of
the patient information for next level review
• Interaction with other Medical review staff to verify information and/or
triage new data issues or prior identified action items
• Attend Kick-Off meetings, weekly team meetings, and client meetings, as
needed or requested.
Qualifications
• Licensed Neurologist with clinical experience.
• Previous experience as a Sub‑Investigator or Principal Investigator (PI) will be highly valued.
• Previous clinical experience.
• English Advanced, mandatory.
• Understanding of clinical/medical data.
• Background in Medical Terminology, Pharmacology, Anatomy, and Physiology
• Excellent motivational, influencing and coaching skills
• Ability to work on multiple projects and manage competing priorities
• Strong customer focus skills
• Ability to establish and maintain effective working relationships with
coworkers, managers and clients
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.