We are on the lookout for a Clinical Data Scientist to join our dynamic team in Newcastle. The successful candidate will analyse clinical data to support studies aimed at improving patient outcomes and enhancing healthcare delivery.
Responsibilities
Design and implement data analysis workflows for clinical trials.
Ensure compliance with Good Clinical Practice (GCP) and other regulatory requirements.
Provide statistical insights to support decision-making in clinical research.
Evaluate and enhance data collection methodologies to improve efficiency.
Maintain thorough documentation of all data analyses and results.
Liaise with external partners regarding data-sharing agreements and collaborations.
Assist in grant writing and the proposal development process for new research projects.
Requirements
Education
Bachelor's degree in a relevant field
Master's degree is preferred
Experience
3+ years of clinical trial experience
Technical Skills
Programming Languages (Python, R)
Clinical Data Management Systems (CDMS)
Soft Skills
Detail-oriented
Project Management
Certifications
Clinical Research Associate (CRA)
GCP Certification
Languages
English: Fluent
Advantageous
Experience with Electronic Data Capture (EDC) systems: Hands-on experience with systems for capturing clinical trial data.
Knowledge of Regulatory Compliance: Understanding of regulatory environments affecting clinical research.
Benefits
Generous pension scheme and employer contributions
Employee assistance programme for mental health support
Paid professional development and training courses
Annual team-building retreat and recognition events
Company Culture
Continuous Improvement: We are committed to continuous improvement in all aspects of our work.
Work-Life Balance: We value the importance of work-life balance and offer flexible working arrangements.
Professional Development: We invest in our employees' growth through ongoing training and mentoring opportunities.