Us Tax Prep & Review Specialist (Cpa/Ea Preferred)

Opsarmy; Quilmes; Remote; ARS 184,482,000 - 276,723,000; Full time

Job summary

Opsarmy seeks a Medical Data Review Manager (Rehumatology) to join our team in a global remote role. The position requires certification in Rehumatology and a medical degree, with strong data review skills to ensure protocol adherence and data readiness for further review.

You'll collaborate with Medical review staff, attend Kick‑Off and client meetings, and oversee data quality across international study sites, ensuring accurate documentation of AE/data and end‑of‑treatment outcomes.

Qualifications

• Bachelor's Degree in Medicine and specialization in Rehumatology (mandatory)
• Advanced English proficiency
• Understanding of clinical/medical data related to trials
• 5 years of related experience in clinical research or CRO/pharmaceuticals

Responsibilities

• Identify anomalies in patient data requiring further investigation with clinical sites
• Review inclusion/exclusion criteria for trial participation
• Review dosing records for adherence to protocol
• Review Adverse Events, concomitant medications, and medical history for consistency with protocol
• Ensure end-of-treatment and end-of-study data are accurately documented
• Review laboratory results for completeness and safety signals
• Communicate with medical review staff and participate in meetings as needed

Skills

Advanced English

Medical data review

Education

Bachelor's Degree in Medicine

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