Data Management and Analysis Specialist in Cirencester

Corin Group is a global orthopaedics innovation business, headquartered in Cirencester, Gloucestershire. We manufacture knee and hip implants that are shipped around the world to provide patients with the best possible outcomes. With over 400 employees, we focus on precision, quality, and customer demand to ensure that we produce a high-quality product at all times.

Due to the exciting growth of Corin, we are now looking to expand our Clinical Affairs Team to continue to meet worldwide demand. We are seeking a highly skilled and detail-oriented Clinical Data Management and Analysis Specialist to join our team. This role will play a key part in supporting global clinical studies, contributing to all aspects of the data management and analysis process—from study start-up through to database lock and post-market activities.

You will work cross-functionally to ensure all clinical data processes meet regulatory standards and contribute to the successful delivery of pre- and post-market clinical evidence for medical devices.

What you'll do:

• Support global clinical study data management activities from start-up to database lock and regulatory submission support.
• Design, implement, validate, and maintain Electronic Data Capture (EDC) systems.
• Contribute to study timelines and ensure key milestones and deliverables are met.
• Review and input into clinical protocols, statistical analysis plans, and clinical study reports.
• Develop and maintain study documentation including CRFs, Data Management Plans, and Data Handling Guidelines.
• Perform programming tasks (e.g. data transfers, data integration, report generation, and statistical outputs) using tools such as R, SQL, Python, or VBA.
• Prepare and analyse clinical datasets (e.g. lab data, imaging, adverse events, and patient-reported outcomes).
• Collaborate with internal teams and external vendors, ensuring high-quality data deliverables.
• Identify and communicate risks to timelines, quality, and budgets.
• Support audits and ensure compliance with regulatory standards and internal SOPs.
• Contribute to process improvements and development within the Data Management function.

Compliance & Standards:

• Ensure adherence to ISO 14155 (Good Clinical Practice) and FDA 21 CFR Part 11.
• Support compliance with ISO 13485 QMS and FDA 21 CFR Part 820 (GMP).
• Contribute to CAPA processes in line with company objectives and SOPs.

About You:

• We are looking for someone who is analytical, adaptable, and proactive, with a passion for clinical data and continuous improvement.
• Bachelor’s degree in Computer Science, Statistics, Biostatistics, Mathematics, or related discipline (or equivalent experience).
• Minimum 2 years’ experience in clinical data management within medical device studies.
• Advanced Microsoft Excel skills.
• Solid understanding of clinical study processes, EDC systems, and data reporting.
• Excellent attention to detail and problem-solving ability.
• Strong written and verbal communication skills.
• Ability to manage multiple priorities in a fast-paced environment.
• Experience working with global clinical studies.

What We Offer:

• Competitive salary and benefits package.
• Opportunity to work on innovative global clinical studies.
• Collaborative and supportive team environment.
• Ongoing professional development and training.
• Career progression opportunities.

If you are looking to take the next step in your clinical data career and contribute to impactful medical device research, we would love to hear from you.

Corin provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, colour, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.