2015 -2018 Director of Clinical and Regulatory Affairs @
2014 -2015 Director, Regulatory Study Start-Up @
2013 -2014 Associate Director, Regulatory Study Start-Up @
2011 -2013 Director, Regulatory and Technical Services @
2011 -2011 Associate Director, Regulatory Affairs and Medical Writing @
2010 -2011 Senior Manager, Medical Writing and International Regulatory Affairs @
2008 -2010 Clinical Trial Regulatory Consultant @
2005 -2008 Medical Writer @
2004 -2005 Post-doctoral Research Fellow @
Stuart Grant Education
University of Strathclyde
PhD, Physiology & Pharmacology
2001-2004
University of Strathclyde
BSc (Hons), Immunology & Pharmacology
1997-2001
Stuart Grant Skills
Clinical Trials
Clinical Development
Oncology
Regulatory Affairs
Orphan Drug Applications
Biotechnology
Study Start-up
DSUR
IND
ICH-GCP
CRO
Clinical Research
Regulatory Submissions
Pharmaceutical Industry
CESP
Clinical Operations
Pharmacology
Cancer Research
Clinical Study Design
Medical Writing
Protocol
Drug Development
Team Leadership
Line Management
SOP development
CTMS
U.S. Food and Drug Administration (FDA)
Consulting
Management
Regulatory Writing
Protocol Development
Phase I
Phase II
Phase III
ISO 14155
Medical Devices
Cardiovascular
Informed Consent
Pharmaceuticals
Clinical Development Plans
Immunology
ProTides
Electronic Common Technical Document (eCTD)
INN
Protocol Writing
Medical Communications
Ich Gcp
MENA
Investigator Brochures
Solid Tumours
Resource Management
Project Finance
Business Development
Prime
Scientific Writing
Strategic Planning
Regulatory Requirements
Phosphoramidate
Microsoft Office
CRO Management
Change Management
Proposal Writing
Regulatory
Editing
Customer Service
U.S. Food And Drug Administration Fda
Hospitals
Fast Track
Electronic Common Technical Document Ectd
Standard Operating Procedure Sop
Physiology
Science
EMA
Pharmacogenomics
MHRA
New Drug Application Nda
Program Management
Project Management
Problem Solving
Standard Operating Procedure
u.s. Food and Drug Administration
Electronic Common Technical Document
New Drug Application
Stuart Grant Summary
Stuart Grant, based in Glasgow, GB, is currently a Senior Vice President, Regulatory Affairs at NuCana plc. Stuart Grant brings experience from previous roles at NuCana plc and inVentiv Health Clinical. Stuart Grant holds a 2001 - 2004 PhD, Physiology & Pharmacology @ University of Strathclyde. With a robust skill set that includes Clinical Trials, Clinical Development, Oncology, Regulatory Affairs, Orphan Drug Applications and more. Stuart Grant has 1 emails and 1 mobile phone numbers on RocketReach.
Looking for a different Stuart Grant?
Find contact details for 700 million professionals.
Get contact details of over 700M profiles across 60M companies - all with industry-leading accuracy. Sales and Recruiter users, try out our Email Finder Extension.
Use our AI-Powered Email Finder
Find business and personal emails and mobile phone numbers with exclusive coverage across niche job titles, industries, and more for unparalleled targeting. Also available via our Contact Data API.