Summary
Overview
Work history
Education
Skills
Certification
LANGUAGES
REFERENCES
CONTACT
Timeline
Generic
Shelley Moore

Shelley Moore

Buckingham,Buckinghamshire

Summary

Experienced Clinical Trials Office Administration Supervisor offering proven record effectively maintaining Trial Matrix files, reliability complying with GCP/ICH guidelines and accurately performing quality control. Awarded and recognised as a dedicated team player who responds to all cross functional departments’ needs and guarantees quality performance. Excels in high-pressure environments using sharp focus, strong attention to detail with a can-do attitude, and personal drive to achieve all goals effectively.

Focused business leader skilled in maintaining regulatory compliance with strict document control and adherence to industry best practices.

Overview

7
7
years of professional experience
1
1
Certification

Work history

Business Administrator for Apprenticeships

The University of Buckingham
2025.04 - Current
  • Managed general enquiries from internal and external stakeholders, overseeing shared inboxes and providing timely, professional responses.
  • Represented the University Apprenticeships Hub at internal and external events, promoting apprenticeship programmes and services.
  • Managed Apprenticeship social media accounts, creating, scheduling and publishing engaging content to promote services and events.
  • Worked across multiple functional areas within the Apprenticeships Team to assist with urgent operational tasks.
  • Supported onboarding processes for new apprentices, ensuring compliance and smooth enrolment.
  • Assisted with internal audits to maintain quality assurance standards.
  • Recorded and analysed payments received, ensuring accurate financial tracking.

Clinical Trials Office & Documentation Supervisor

Vitalograph
2024.10 - 2025.04
  • Lead a team of 10, delegating tasks and monitoring performance to meet project deadlines.
  • Owner of all Clinical Trials Documentation Administration processes
  • SME of eTMF
  • Leading the completion of Project File Reviews
  • Monitor trial progress closely, implementing corrective actions swiftly to address any deviations from the plan.
  • Respond to audit findings promptly, addressing discrepancies and implementing recommendations to improve trial conduct.
  • Ensured rigorous adherence to Good Clinical Practice GCP guidelines, maintaining high standards of research integrity.
  • Review and update Standard Operating Procedures
  • Rota Management
  • Diary Management
  • Recruitment/Preparing Induction Plans

Clinical Trials Office & Administration Supervisor

Vitalograph
Maids Morton
2022.02 - 2024.10
  • Rota management
  • Liaising with Facilities for required change/maintenance of the office space
  • Ownership of the Clinical Trials and Data Management Administrative processes, to identify & implement process improvements for efficiency & effectiveness
  • Proactively monitoring document approval dates in PM system following-up with Project team to obtain final documents for filing
  • Leading the completion of Project File Reviews according to schedule
  • Supporting of Archiving of Project documentation
  • Supporting QA with Audits
  • Preparing Induction plans for new CT and DM staff
  • Organising internal training sessions for all UK CT and DM staff, in collaboration with the Training Team
  • Line Management of CT Administrative staff
  • Supporting Recruitment of other CT staff as requested by Line Management
  • Diary Management of Senior staff & Meeting rooms
  • Organising Team building and social events/meeting, including making travel arrangements for attendees when necessary

Administration Assistant

Vitalograph
Maids Morton, BKM
2019.07 - 2022.02
  • Document Control, including printing, scanning Filling & record-keeping
  • Supporting administration of internal training
  • QC checks
  • Supporting of Archiving of Project documentation
  • Supporting the Project Management team with general admin as requested
  • Assisting in document creation and approval process
  • Assisting with reviewing project documentation to schedule
  • Working with QA to implement best practices for documentation control procedures and identify improvement
  • Organise events & meetings

Education

NVQ Level 2 - Beauty Therapy Beauty

Milton Keynes College
Milton Keynes

X6 A-D GCSE’s - undefined

Kingham Hill School
Chipping Norton

Skills

  • Line Management
  • SME of eTMF
  • Ensures adherence to standard operating procedures, GCP, and FDA regulations with strong understanding of inspection readiness
  • Tracking study status
  • Database administration
  • Demonstrated knowledge and experience in regulatory aspects of pharmaceutical
  • Multitasking Abilities
  • Training and Development
  • Demonstrated ability to work independently with exceptional organization and attention to detail

Certification

ILM Level 3 Award in Leadership and Management

LANGUAGES

English

REFERENCES

References available upon request.

CONTACT

  • Buckingham, Buckinghamshire MK18 7BR
  • 0750815598
  • Shelleymoore85@gmail.com

Timeline

Business Administrator for Apprenticeships

The University of Buckingham
2025.04 - Current

Clinical Trials Office & Documentation Supervisor

Vitalograph
2024.10 - 2025.04

Clinical Trials Office & Administration Supervisor

Vitalograph
2022.02 - 2024.10

Administration Assistant

Vitalograph
2019.07 - 2022.02

X6 A-D GCSE’s - undefined

Kingham Hill School

NVQ Level 2 - Beauty Therapy Beauty

Milton Keynes College
Shelley Moore