Miri P.

Key Skills

Software

Other

Top Subject Matter

Clinical trials (site feasibility, oncology/IBD/respiratory and other indications) document management

Clinical trials monitoring and onsite data integrity/data quality oversight

Legal Services & Contract Review

Top Data Types

Document

Text

Top Task Types

Data Collection

Freelancer Overview

Clinical Operations Assistant (Feasibility task), PAREXEL International, Korea. Brings 6+ years of professional experience across complex professional workflows, research, and quality-focused execution. Core strengths include Other. Education includes Bachelor of Engineering, Konkuk University (2020). AI-training focus includes data types such as Document and labeling workflows including Data Collection.

Labeling Experience

Clinical Research Associate I, PAREXEL International, Korea

OtherDocumentData Collection

Ensured data quality and data integrity at clinical sites by identifying potential data quality/data integrity issues and implementing appropriate follow-up actions. Acted as the direct contact for assigned sites, supporting adherence to study protocol and training requirements, and addressing documentation and communication deficiencies. Conducted follow-ups for issues pending from previous visits and resolved site problems impacting study timelines. •Monitored protocol adherence and performed problem-solving at clinical sites •Evaluated and resolved documentation gaps and training needs •Followed up on site-related questions and immediate-action study issues •Communicated study non-compliance impacts with resolution strategies

2023 - 2025

Clinical Operations Assistant (Feasibility task), PAREXEL International, Korea

OtherDocumentData Collection

Supported feasibility and trial document organization by tracking, scanning, coding, and applying naming conventions for documents sent to PMED work-in-progress and central file areas. Performed filing and archiving of paper documents and maintained basic quality checks to ensure accurate maintenance of clinical trial records. Organized translations of study documents and supported administrative data handling for site documentation and internal requests. •Tracked and maintained clinical trial management system (CTMS) and site trackers •Executed document coding, scanning, and centralized storage workflows •Collected internal signatures for site documents in accordance with internal processes •Coordinated courier shipments and internal finance follow-ups related to study documentation

2020 - 2023

Education

Work History