Us Tax Preparation & Review Specialist

Opsarmy; Quilmes; Remote; ARS 107,614,000 - 169,108,000; Full time

Job summary

Opsarmy seeks a Medical Data Review Manager (Rehumatology) to oversee remote, international reviews of structured clinical data for global trials. The role is full-time and requires a medical degree with Rehumatology specialization.

The candidate will verify data plausibility, review inclusion/exclusion criteria, dosing records, adverse events, and end-of-study information, coordinating with the medical review team to ensure readiness for next review stage.

Qualifications

• Advanced English required with strong communication skills.
• 5 years of clinical research experience at site, CRO, or pharma.
• Experience as Sub-Investigator or Principal Investigator is valuable.

Responsibilities

• Identify anomalies in patient data and coordinate with clinical site for verification.
• Review inclusion/exclusion criteria to ensure proper trial eligibility.
• Assess dosing records for protocol adherence and identify discrepancies.
• Evaluate reported Adverse Events and medical history for consistency with protocol.
• Ensure end-of-treatment/study information is accurately documented.

Skills

Advanced English

Clinical research experience

PI/Sub-Investigator experience

Education

Bachelor's Degree in Medicine

Specialized in Rehumatology

Job description

Medical Data Review Manager (Rehumatology)

Buenos Aires, Argentina
São Paulo, Brazil
Full time
R
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