At a Glance
- Tasks: Coordinate clinical data for groundbreaking trials and ensure quality outcomes.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Enjoy a competitive salary, flexible working, and opportunities for professional growth.
- Other info: Home-based role with a dynamic team and excellent career advancement potential.
- Why this job: Make a real difference in patient outcomes while working with innovative medical treatments.
- Qualifications: Bachelor's degree or relevant experience, plus 3 years in data management required.
The predicted salary is between 36900 - 45100 £ per year.
The Senior Clinical Data Coordinator performs activities pertaining to the conduct of Phase I-Il I clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant procedures and guidelines to ensure that a quality work product is produced and timelines and deliverables are met.
Summary of the Essential Functions of the Job Perform ongoing data review, including reconciliation of third party data streams and serious adverse event reconciliation with the safety database.
Perform User Acceptance Testing (UAT) of clinical databases.
Perform Quality Control (QC) of clinical databases.
Perform ongoing updates of Data Management-related documentation, as needed.
Minimum Requirements Bachelor's degree OR certification in a related allied health profession from an appropriately accredited institution (i. e.
RN, MT, PA, RT) is preferred, but individuals with commensurate experience will be considered.
Minimum of 3 years of data management experience is required.
Experience with Electronic Data Capture (EDC) system(s) is required- Oracle Inc.'s Inform EDC system is preferred.
Oncology and/or inflammatory therapeutic area experience This role is not eligible for UK visa sponsorship IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Learn more at IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.
All information and credentials submitted in your application must be truthful and complete.
Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law.
We appreciate your honesty and professionalism.
Summary
Location: Reading, Berkshire, United Kingdom; Manchester, United Kingdom; Livingston, West Lothian, United Kingdom; London, United Kingdom
Type: Full time
Senior Clinical Data Coordinator - FSP (Homebased - UK) in Livingston employer: IQVIA
IQVIA in Livingston, Scotland is an excellent employer that fosters a collaborative team environment and prioritises employee growth through outstanding career development opportunities. Working as a Lab Operations Assistant here not only allows you to contribute to meaningful projects but also ensures you are part of a supportive workplace that values safety and professionalism.
