Experience

Pfizer UK
• United Kingdom
• Pharmaceutical Manufacturing
• 1 - 100 Employee
• Associate Director Patient Recruitment Strategy

  • Jul 2023 - Present

Innovative Trials
• United Kingdom
• Pharmaceutical Manufacturing
• 1 - 100 Employee
• Patient Recruitment Manager

  • Feb 2023 - Jul 2023


Syneos Health

• United States
• Biotechnology Research
• 700 & Above Employee

• Patient Engagement Lead

  • Oct 2022 - Feb 2023

  • Proactively identifies additional strategies to support patient enrolment, compliance, and retention. Leads discussion with study team and clients to illustrate the added value for each tactic • Serves as a mentor and provides project management oversight to team members • Leads and participates in change initiatives • Leads the development, preparation, regulatory approval, and distribution of materials relating to Patient Engagement tactics from sponsor contracting through to… Show more • Proactively identifies additional strategies to support patient enrolment, compliance, and retention. Leads discussion with study team and clients to illustrate the added value for each tactic • Serves as a mentor and provides project management oversight to team members • Leads and participates in change initiatives • Leads the development, preparation, regulatory approval, and distribution of materials relating to Patient Engagement tactics from sponsor contracting through to closure of Patient Engagement activities • Collaborates with client to define advocacy strategy. Supports development of advocacy materials and IRB submission. • Able to identify quality issues, escalate appropriately and manage issues to closure; sharing lessons learned and refining processes. • Leads development of the Patient Engagement Plan • Ensure vendor is qualified and contracted per company SOPs/WIs. Identify and independently resolve vendor related issues • Ensures all project deliverables meet customer expectations including contracted deliverables, provision of accurate projections, reports and updates, together with ongoing risk assessment and proactive mitigation strategies. Documents scope changes. • Manage project within contracted direct and indirect budgets, and timeline ensuring any out-of-scope activities are not initiated prior to being documented via budget update, communicated to the project management team, and approved by the sponsor.

• Senior Patient Engagement Specialist

  • Dec 2019 - Oct 2022



University of Surrey

• United Kingdom
• Higher Education
• 700 & Above Employee

• Research Integrity and Governance Coordinator

  • Aug 2018 - Nov 2019

• Project Manager (clinical trials)

  • May 2017 - Jul 2018

  - Responsible for coordination and management of CTIMP and non-CTIMP studies - Responsible for the production and management of study timelines - Primary contact for sponsor and study teams - Ensure that studies are conducted in compliance with national guidelines and local SOPs - Development of study documents - Financial tracking and invoicing against study milestones - Produce study reports - Oversight of data review and database lock

• Research Integrity and Governance Coordinator

  • Dec 2016 - May 2017

  -Coordinate and track University Ethics Committee applications -Complete research governance checks application to Research Ethics Committees -Support running of training sessions -Led team meetings

• Clinical Research Recruiter

  • Jul 2015 - Dec 2016

  - Responsible for recruiting study participants using a variety of media - Production of study specific documents - Effectively coordinated participants’ study journey - Managed participant database



University of Reading

• United Kingdom
• Higher Education
• 700 & Above Employee

• Research Technician

  • Apr 2014 - Jun 2015

  - Production of scientific and technical reports for industrial collaborators. - Accountable for running chemical analyses on samples and analysing the data. - Organised consumer trials and successfully led sensory panels. - Production of scientific and technical reports for industrial collaborators. - Accountable for running chemical analyses on samples and analysing the data. - Organised consumer trials and successfully led sensory panels.