Clinical Data Coordinator | Remote

N2S Global Workforce Solutions LLC; Manila; Remote; PHP 500,000 - 700,000; Full time

Job summary

N2S Global Workforce Solutions LLC is seeking a detail-oriented Clinical Data Coordinator to support clinical data management activities and ensure the accuracy, integrity, and quality of clinical trial data. This remote role emphasizes data review, reconciliation, and discrepancy management.

Responsibilities include running SAS programs, data cleaning, managing data queries, and monitoring study metrics. Ideal candidates hold a Bachelor's degree with at least 1 year in CDM and strong English

Qualifications

• Bachelor's degree in a relevant field.
• At least 1 year of Clinical Data Management experience in biotech, pharma, or CRO.
• Strong computer skills and ability to learn new applications.
• Excellent attention to detail, organization, and time management.
• Strong written and verbal English communication skills.
• Knowledge of CDISC standards (CDASH/SDTM) is an advantage.
• Familiarity with clinical trials, GCP, and ICH guidelines is an advantage.

Responsibilities

• Support clinical data review, reconciliation, and discrepancy management.
• Run SAS programs, review data listings, and assist with data cleaning activities.
• Manage data queries and report potential protocol deviations.
• Monitor study metrics and prepare data status and ad-hoc reports.
• Perform User Acceptance Testing (UAT).
• Maintain CDM documentation and TMF records.
• Support Lead Data Managers in ensuring data quality and regulatory compliance.

Skills

Attention to detail

Time management

English communication

Education

Bachelor's degree

Tools

SAS

Job description

Clinical Data Coordinator | Remote

We are looking for a detail-oriented Clinical Data Coordinator to support clinical data management activities and ensure the accuracy, integrity, and quality of clinical trial data.

Key Responsibilities

• Support clinical data review, reconciliation, and discrepancy management.
• Run SAS programs, review data listings, and assist with data cleaning activities.
• Manage data queries and report potential protocol deviations.
• Monitor study metrics and prepare data status and ad-hoc reports.
• Perform User Acceptance Testing (UAT).
• Maintain clinical data management documentation and Trial Master File (TMF) records.
• Support Lead Data Managers in ensuring data quality and compliance with regulatory requirements.

Qualifications

• Bachelor's degree in a relevant field.
• At least 1 year of Clinical Data Management experience in the biotechnology, pharmaceutical, or Clinical Research Organization (CRO) industry.
• Strong computer skills and ability to learn new applications.
• Excellent attention to detail, organization, and time management skills.
• Strong written and verbal English communication skills.
• Knowledge of CDISC standards (CDASH/SDTM) is an advantage.
• Familiarity with clinical trials, Good Clinical Practice (GCP), and ICH guidelines is an advantage.