This is a fully remote position, open to applicants in United Kingdom.

📋 Description

• Conduct continuous data assessments, including the reconciliation of external data streams and serious adverse event reconciliation with the safety database.

• Execute User Acceptance Testing (UAT) for clinical databases.

• Carry out Quality Control (QC) for clinical databases.

• Update Data Management-related documentation on an ongoing basis as necessary.

• Undertake activities related to Phase I-III clinical trials in compliance with ICH/Good Clinical Practices (GCP) and applicable procedures and guidelines.

• Ensure that quality work products, timelines, and deliverables are achieved.

⛳️ Requirements

• A bachelor's degree or certification in a related allied health profession from an accredited institution (e.g., RN, MT, PA, RT) is preferred; equivalent experience may be taken into account.

• At least 3 years of data management experience is required.

• Proficiency with Electronic Data Capture (EDC) systems is mandatory.

• Familiarity with Oracle Inc.'s Inform™ EDC system is preferred.

• Experience in oncology and/or inflammatory therapeutic areas.

• Must not require sponsorship for a UK visa.