Medical Data Review Manager Rheumatology

IQVIA; Buenos Aires; À distance; ARS 136 254 000 - 196 812 000; Plein temps

Avantages offerts par ce poste

Remote work

Résumé du poste

IQVIA is seeking a Medical Data Review Manager to join our team. This is a home-based, global scope position with mandatory Rheumatology specialization and medical degree requirements.

The role focuses on data plausibility, protocol adherence, and comprehensive patient information readiness for next review stages. The candidate will review clinical data, ensure accurate documentation, and collaborate with a global team including sub-investigators and PI experience.

Qualifications

• Advanced English required for global communications.
• Experience with clinical data in trials and data review processes.
• Strong understanding of medical terminology and pharmacology concepts.
• Experience as Sub-Investigator or Principal Investigator is relevant.

Responsabilités

• Identify anomalies in patient data that require site clarification.
• Review inclusion/exclusion criteria for trial eligibility.
• Check dosing records for protocol adherence and accuracy.
• Review adverse events, concomitant medications, and medical history for consistency.
• Ensure end-of-treatment (EOT) and end-of-study (EOS) documentation and reasons for discontinuation.
• Review laboratory results for completeness and safety signals.
• Review any other information to determine readiness for next review.
• Collaborate with Medical Review staff to triage issues and discuss data.
• Attend Kick-off, weekly team, and client meetings as needed.

Connaissances

Advanced English

Clinical data review

Medical terminology

PI/Sub-Investigator experience

Formation

Bachelor's Degree in Medicine

Specialization in Rehumatology

Description du poste

We are looking for a Medical Data Review Manager to join our team!

*Home based - global scope position.

* Specialization in Rehumatology (certified - mandatory).

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, graduated and specialized in Rehumatology (mandatory - we can only consider physicians for this role).
• 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.