Medical Data Review Manager

IQVIA LLC; Buenos Aires; Híbrido; ARS 136.360.000 - 196.964.000; Jornada completa

Descripción de la vacante

IQVIA LLC seeks a Medical Data Review Manager for a home-based, global role. You will review structured clinical patient data to verify plausibility and protocol adherence, enabling next-level review.

Key tasks include identifying data anomalies, validating inclusion/exclusion criteria, and assessing dosing records, AEs and medical history for data integrity. Advanced English and a medical degree are required.

Formación

• Bachelor's Degree in Medicine is mandatory.
• Advanced English required for global scope.
• Experience with clinical research and data review processes.
• Understanding of medical terminology, pharmacology, anatomy and physiology.

Responsabilidades

• Identify anomalies in patient data requiring investigation with clinical sites.
• Review inclusion/exclusion criteria to confirm patient eligibility for trials.
• Review dosing records for protocol adherence and accuracy.
• Assess adverse events, concomitant medications and medical history for consistency.
• Ensure EOT and EOS data are documented and explain reasons for participation changes.
• Review laboratory results for completeness and protocol alignment.
• Coordinate with medical review staff and triage data issues; participate in meetings.

Conocimientos

Advanced English

Medical terminology

Communication skills

Coaching

Stakeholder management

Educación

Bachelor's Degree in Medicine

Descripción del empleo

We are looking for a Medical Data Review Manager to join our team! *Home based - global scope position. 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

• Bachelor's Degree in Medicine (mandatory - we can only consider physicians for this role). Graduated.
• 5 years of related experience in clinical research - research site level or CRO/Pharmaceutical companies. Experience as Sub-Investigator or Principal Investigator are relevant.
• Advanced English level - great communication skills in the language. The role has a global scope.
• Understanding of clinical/medical data related to clinical trials.
• 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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Thank you for your interest in growing your career with us.