Clinical Research Study Configuration & CRIO Support Agent

Company: Aegle Management LLC

Location: Office in Karachi

Shift: U.S. healthcare hours preferred

Type: Full-time / Contract-based

Aegle Management LLC is hiring an experienced Clinical Research Operations Agent, This role is ideal for someone who understands clinical research studies, study protocols, CRIO configuration, e-source templates, data review, and sponsor EDC workflows.

The selected candidate will support the remote research operations team by helping configure studies, organize source documents, review clinical data, and assist with accurate study documentation.

Key Responsibilities

• Review and understand clinical study protocols.
• Configure new studies in CRIO.
• Create and maintain e-source templates based on study requirements.
• Add visits, procedures, assessments, forms, and study workflows in CRIO.
• Maintain a proper source library for reusable study templates.
• Review coordinator-entered data for accuracy and completeness.
• Identify missing, incomplete, or inconsistent study documentation.
• Support transfer of data from CRIO to sponsor EDC systems.
• Coordinate with research coordinators and site teams for corrections.
• Track study setup progress, open issues, pending forms, and completion status.
• Maintain confidentiality and follow clinical research documentation standards.

Required Experience

• Prior experience in clinical research operations or study coordination.
• Hands-on experience with CRIO is strongly preferred.
• Understanding of study protocols, visit schedules, procedures, and source documentation.
• Experience with e-source creation, study setup, or EDC data entry.
• Good understanding of clinical trial documentation and data quality.
• Strong attention to detail.
• Good English communication skills.
• Ability to work independently with minimal supervision.

Preferred Skills

• Experience with sponsor EDC platforms.
• Knowledge of GCP, clinical trial workflows, and audit readiness.
• Experience working with U.S.-based research sites.
• Ability to convert protocol requirements into structured CRIO forms.
• Familiarity with screenings, audits, research trackers, and coordinator workflows.

Ideal Candidate

We are looking for someone who is not just a data entry operator, but someone who understands how a clinical research study works from the inside — protocol review, study build, e-source configuration, coordinator support, audit checks, and data transfer to EDC.

This person should be reliable, detail-oriented, and capable of becoming a long-term part of Aegle’s research operations support team.

Requirements added by the job poster

• Can start immediately

• Working in an onsite setting

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