Job Overview
We are seeking a highly skilled and detail-oriented Clinical Database Administrator to join our team. This role involves managing and maintaining clinical trial databases, ensuring data integrity, compliance with regulatory standards, and supporting clinical research activities. The successful candidate will play a vital part in advancing medical research by providing accurate and reliable data management solutions within a dynamic healthcare environment. Prior experience in clinical research, data management, and compliance is essential for this position.
Duties
- Develop, implement, and maintain secure clinical databases in accordance with FDA regulations and industry standards.
- Oversee data entry, validation, and quality control processes to ensure accuracy and completeness of clinical trial data.
- Monitor patient data collection processes, ensuring adherence to protocol requirements and patient safety guidelines.
- Utilise statistical software to analyse data trends and generate reports for research teams and regulatory submissions.
- Ensure compliance with all relevant regulations, including FDA guidelines and Good Clinical Practice (GCP).
- Supervise junior staff or interns involved in data entry or management tasks, providing training and oversight as necessary.
- Collaborate closely with clinical research teams, nurses, phlebotomists, and other healthcare professionals to facilitate smooth data flow.
- Maintain meticulous documentation of database modifications, audit trails, and validation procedures for regulatory inspections.
- Assist in the development of standard operating procedures (SOPs) related to data management activities.
Requirements
- Proven experience in clinical research or healthcare settings with a strong understanding of medical terminology.
- Demonstrated analysis skills with proficiency in statistical software packages such as SPSS, SAS or R.
- Knowledge of patient monitoring protocols and clinical trial processes.
- Familiarity with FDA regulations, GCP guidelines, and compliance management practices.
- Expertise in data management systems specific to clinical research environments.
- Supervising experience within a healthcare or research context is highly desirable.
- Nursing qualification or experience in phlebotomy is advantageous but not mandatory.
- Excellent organisational skills with the ability to manage multiple projects simultaneously while maintaining attention to detail.
- Strong communication skills to effectively liaise with multidisciplinary teams and regulatory bodies.
This position offers an engaging opportunity for professionals committed to advancing medical science through meticulous data management within a regulated environment. The ideal candidate will be proactive, organised, and dedicated to maintaining the highest standards of compliance and accuracy in clinical research data handling.
Pay: £30,798.55-£38,212.23 per year
Benefits:
- Company pension
- Employee mentoring programme
- Free parking
- On-site parking
Work Location: In person
