Clinical Data Manager: Lead Data Quality in Global Trials

IQVIA; Reading; On-site; GBP 50,000 - 70,000; Full time

Job summary

IQVIA is seeking a Clinical Data Manager to oversee data management activities for Phase I-III trials in accordance with ICH/GCP. You will ensure timely, budget-conscious data delivery with high quality, working with multidisciplinary project teams.

The role requires 5+ years in data management, Oracle Inform EDC experience, and CRO/pharma background. Oncology/inflammatory experience is preferred. This position is based in Reading, UK, with no visa sponsorship.

Qualifications

• Minimum of 5 years of data management experience.
• Bachelor's degree or allied health certification preferred.
• Oracle Inform EDC experience required.
• Oncology and/or inflammatory therapeutic area experience preferred.
• Project management experience within Data Management preferred.
• CRO or Pharma data management experience desirable.

Responsibilities

• Participate as the primary data management representative on multidisciplinary project teams and ensure effective communication exchange.
• Communicate key clinical data management metrics and determine actions with study team.
• Review, develop and/or write trial documents including CRFs, edit checks, DMPs and eCRF guidelines.
• Participate in UAT and QC activities as needed.
• Collaborate with Clinical Database Programmers on data flow charts and transfer specs.
• Assist with site and vendor training on CDM topics.
• Provide data review training and guidance to Sr. Clinical Data Coordinators.
• Perform data review and discrepancy resolution as needed.
• Archive trials and documentation after completion.
• Ensure adherence to GCP and applicable regulations.

Skills

Data management

Communication

Project management

Oracle Inform EDC

Clinical trial documentation

Quality control

Education

Bachelor's degree

Allied health certification

Tools

eCRF systems

Job description

IQVIA is seeking a Clinical Data Manager to oversee data management activities for Phase I-III trials in accordance with ICH/GCP. You will ensure timely, budget-conscious data delivery with high quality, working with multidisciplinary project teams.

The role requires 5+ years in data management, Oracle Inform EDC experience, and CRO/pharma background. Oncology/inflammatory experience is preferred. This position is based in Reading, UK, with no visa sponsorship.