Clinical Data Reviewer.

PSI; Buenos Aires; Remote; ARS 40,000 - 70,000; Full time

Job summary

PSI is seeking a dedicated Clinical Monitoring professional to help monitor study data remotely, identify data integrity issues, and support risk-based monitoring activities. You will work with a closely-knit team to ensure participant safety and high-quality data across studies.

The role emphasizes analytical thinking, data-driven problem solving, and collaboration within a dynamic clinical operations environment.

Qualifications

• Bachelor’s degree in a relevant field.
• At least 1 year of experience in the Clinical Research Industry.
• Clinical Monitoring experience is an advantage.
• English proficiency at CEFR B2 level or above.
• Proficiency in MS Office applications.
• Analytical mindset and attention to detail.
• Ability to learn, plan and work effectively in a dynamic team environment.

Responsibilities

• Review clinical data remotely and identify errors, systemic issues and trends related to data integrity, participant safety and site performance.
• Generate, follow up and resolve data queries and site issues, and identify potential protocol deviations.
• Develop and maintain study-specific Central Data Review tools, templates and tracking materials.
• Support the setup and management of risk-based and central monitoring tools and activities.
• Assist with central monitoring signal review, root cause investigation and follow-up.
• Support the Central Monitoring Manager with study data, documents and reports.
• Contribute to inspection readiness, including eTMF QC and study archive activities.

Skills

Analytical mindset

Attention to detail

Teamwork

Education

Bachelor’s degree

Tools

MS Office

Job description

Job Description

You will join a widespread, yet closely-knit team with the same mentality and desire to develop smart and intelligent approach to project monitoring. You will help to shape the future of effective risk-based monitoring at PSI and ensure higher quality of study data. You will spend time monitoring study data remotely, identifying errors and issues with site performance.

You will:

Review clinical data remotely and identify errors, systemic issues and trends related to data integrity, participant safety and site performance Generate, follow up and resolve data queries and site issues, and identify potential protocol deviations Develop and maintain study-specific Central Data Review tools, templates and tracking materials Support the setup and management of risk-based and central monitoring tools and activities Assist with central monitoring signal review, root cause investigation and follow-up Support the Central Monitoring Manager with study data, documents and reports Contribute to inspection readiness, including eTMF QC and study archive activities

Qualifications

Bachelor’s degree At least 1 year of experience in the Clinical Research Industry Clinical Monitoring experience is an advantage English proficiency at CEFR B2 level or above Proficiency in MS Office applications Analytical mindset and attention to detail Ability to learn, plan and work effectively in a dynamic team environment

Additional Information

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.