Clinical Trials Compliance Associate II - Data Integrity

ThermoFisher Scientific; Glasgow; On-site; GBP 26,000 - 38,000; Full time

Job summary

Thermo Fisher Scientific is seeking an on-site Clinical Data Entry/Documentation support role in Glasgow to assist with accurate data capture for clinical studies. You will manage study trackers, ensure proper eCRF entries from source notes, and help resolve data queries under supervision.

The position emphasizes adherence to ICH/GCP guidelines, strong attention to detail, and effective communication with monitors and sponsors in a busy office environment.

Qualifications

• High/Secondary school diploma or equivalent and relevant formal academic / vocational qualification.
• Technical positions may require a certificate.
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 2 years).
• Familiarity with ICH/GCP guidelines and data protection regulations is desirable.

Responsibilities

• Maintains ISF and study trackers and supports verification that ICFs are correctly completed.
• Assists with data capturing activities and ensures accurate entry of data in the eCRF from source notes.
• Verifies protocol visit windows and reports deviations/Quality Incidents, supporting investigations and resolutions.
• May assist monitors and sponsor representatives with query resolutions after monitoring visits; escalate to management as needed.

Skills

Data entry

Interpersonal skills

Business English

MS Office

Medical terminology

Attention to detail

Education

High/Secondary diploma

Certificate (technical)

2+ years relevant experience

Tools

eCRF systems

Job description

Thermo Fisher Scientific is seeking an on-site Clinical Data Entry/Documentation support role in Glasgow to assist with accurate data capture for clinical studies. You will manage study trackers, ensure proper eCRF entries from source notes, and help resolve data queries under supervision.

The position emphasizes adherence to ICH/GCP guidelines, strong attention to detail, and effective communication with monitors and sponsors in a busy office environment.