Clinical Data Manager in Liverpool - CV-Library

Clinical Data Manager – £35,000-£47,000 per annum– Liverpool / Hybrid

The Role

Do you have a keen eye for detail and a knack for ensuring data accuracy? Are you excited about using cutting-edge AI to transform healthcare?

MyCardium AI, a rapidly growing company using AI to revolutionise cardiac MRI analysis, is seeking a highly motivated Clinical Data Manager to join our team in Liverpool.

In this pivotal role, you will oversee the collection, management, and analysis of imaging data from clinical trials. You'll ensure data quality and integrity, working closely with a dynamic team to achieve our mission of improving patient outcomes.

Key Responsibilities:

Develop and manage data systems for imaging studies.
Ensure adherence to regulatory standards and study protocols.
Collaborate with investigators and statisticians to define data collection needs.
Oversee data entry and validation for accuracy, completeness, and consistency.
Implement quality control processes to identify and resolve data issues.
Manage data transfers and ensure correct formatting.
Prepare and review data reports for internal and external stakeholders.
Utilise Python and R scripting for data analysis.
Partner with the Core Lab team to develop and improve data management tools.
The Company

Founded in 2022, MyCardium AI is a spin-out from University College London. Our aim is to transform healthcare delivery using AI for cardiac MRI analysis. We're a passionate team committed to excellence, innovation, and creating a positive and inclusive work environment.

The Benefits

Competitive salary and benefits package (£35,000-£47,000 per annum).
Be part of a dynamic, innovative team in a rapidly growing field.
Make a significant impact on developing new treatments.
Hybrid working (Liverpool HQ/remote).
The Person

Bachelor's degree in Life Sciences, Biostatistics, Computer Science or similar.
Minimum 3 years' experience in clinical data management, ideally in imaging.
Experience with imaging data and software (PACS, DICOM).
Knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
Proficiency in data management software and databases.
Strong understanding of clinical trials and regulations.
Excellent organisation and communication skills.
Ability to work independently and collaboratively.
Certification in Clinical Data Management (CDDM) desirable.
If you are keen on joining this exciting, forward-thinking company and taking the next step in your career, then please click the apply now button to find out more