Stephen Kinton Email & Phone Number

Leeds, UK

Continuation of my prior role at Labcorp. Fortrea spun out from Labcorp as an independent clinical development focused CRO in mid-2023. Leadership of Business Development Directors spread across the EU and US for Fortrea's clinical pharmacology division. Encompassing biotech, pharma and strategic partnership/alliance accounts.

Leeds, United Kingdom

Leadership of Business Development Directors spread across the EU and US for Labcorp's clinical pharmacology division. Encompassing biotech, pharma and strategic partnership/alliance accounts.

Leeds, United Kingdom

Management of the European business development team for Covance's clinical pharmacology division, reporting to VP, Business Development in the US. Responsible for business relationships with our EU strategic partners and biotech accounts. Other responsibilities as per prior role.

Leeds, United Kingdom

Management of the European business development team for Covance's phase I and II division, reporting to Global Executive Director in the US. Player/Coach role encompassing line management of EU BD team whilst covering the UK and Israel territory.

Leeds, United Kingdom

• Business development lead for Covance's phase I and II division, primarily covered the UK, Germany and Israel carrying a multi-million dollar annual target. Also covered Spain, Italy, France and Portugal at various.
• Generate new business leads across all types of sponsors; from virtual biotech to large pharma companies
• Manage and develop multiple key accounts
• Maintain broad network of industry contacts
• Lead proposal development, providing overall direction
• Lead bid defence team; preparation through to delivery

Leeds, West Yorkshire

• Co-ordinate production of proposals for phase I and II studies
• Negotiate pricing, contracts (subcontractor, consulting, vendor, indemnity and master service agreements), payment schedules and study timelines
• Review confidentiality, study and subcontractor agreements

Leeds, West Yorkshire

• Co-ordinate, conduct and lead audits across the entire business in compliance with GCP, GMP and GLP (GxP) regulations, as well as external investigator sites and subcontractors.
• Host sponsor audits and MHRA inspections
• Carry out a variety of study, process, facility, IT, investigator site and subcontractor /vendor audits
• Auditing protocols, Case Report Forms (CRF) as well as pre-clinical and clinical study reports
• Write detailed audit reports and present findings to auditees and management.
• Write new SOPs and review current SOPs for regulatory compliance.

Windlesham, Surrey

• Phase II to IV - Assigned to oncology and neuroscience therapeutic areas
• Responsible for expedited reporting for oncology and neuroscience products to the EMEA, FDA, investigators and ethics committees, as well as government body’s world wide.
• Responsible for the daily triage of cases - determining timeline and assigning cases for entry.
• Manage adverse event and device reports; responsible for initial review, assess event expectedness against product label information.
• Work closely with global affiliates to achieve quality and timely follow up information

Alderley Park, Cheshire

• Assigned to cardiovascular therapeutic area on large Phase III trial
• Worked on both Electronic Data Capture (EDC - Oracle InForm) and traditional paper CRF studies
• Responsible for verification, validation, generation of queries and database updates
• Involved in SAE reconciliation in conjunction with the pharmacovigilance team and the clinical study team
• Involved in data management Quality Control activities
• Production of study level clinical data management documents, user acceptance testing, and the co-ordination, training and support of internal and external staff