Clinical Research Graduate Trainee

at  Optos

MINIMUM QUALIFICATIONS

• BA/BSc in STEM (science, technology, engineering, or mathematics) related field required.
• Excellent practical experience by demonstrating methodical and logical thought process.
• Must have a high sense of urgency and decisiveness; results, action, and detail-oriented approach.
• Must be able to work well in a cross-departmental and multinational team environment, excellent communication skills.
• Ability to multi-task with changing priorities.
• A good understanding of programming concepts. Experience in structured queries or object-oriented language (i.e. SQL, python) preferred.

ROLE SUMMARY

We are currently looking for a Clinical Research Graduate Trainee to join our Clinical team based in Dunfermline. This is a fantastic opportunity to join a highly motivated team in assisting with the setup and maintenance of systems used in the collection of data for clinical trials and image processing. You will be responsible for the co-ordination, output, maintenance and reconciliation of data generated from the clinical systems in association with internal processes. The role will also require the successful candidate to review and QC clinical study images.

ESSENTIAL DUTIES AND RESPONSIBILITIES

• Contribute to the development of Data Management specific documents.
• Contribute to the system design specifications and other technical CDM documents.
• Create or contribute to robust, well documented programming code.
• Develop and maintain test scrips, as well as user acceptance testing.
• Support all phases of testing by efficiently diagnosing and resolving defects.
• Integrate implemented code and database objects.
• Data extractions from the internal systems and structured data.
• User Management – eDC and Optos Advance systems.
• Review, reconciliation and QC of clinical and image data.
• Data review, data cleaning, and follow-up until data cleaning final.
• Contribute to the database launch, maintenance, and lock.
• Create tracker for image processing.
• Review and QC images.
• Ability to work within standardised work environment to follow ICH/FDA/MDR regulations.
• Perform other duties as required by the position.