VP Statistical Strategic Consultancy

Veramed is looking for an ambitious and forward thinking senior statistical leader to drive the growth and direction of our statistical services. The VP/SVP S..S..C will shape strategy, ensure technical excellence and collaborate across business units to fuel innovation.

You’ll provide high-impact leadership in commercial and technical domains—guiding proposals, RFPs and bid defences—while mentoring teams and championing thought leadership through publications, conferences, and webinars.

Exceptional communication and strategic vision are a must. With an MSc or PhD in Statistics and 15+ years in pharma/CROs, you’ll bring expertise in regulatory interactions, statistical initiatives, and program management from development to submission.

Location:

• Open to consider UK/US/EU for the right candidate

Responsibilities:

• Defining & delivering the strategy for growth in statistical service lines (FSP, Consultancy, Projects, DMC) in collaboration with business development and business unit leads
• Provision of statistical technical leadership supporting commercial activities, including RFPs, proposals, bid defences
• Provision of statistical leadership across the business, including
• Statistical advice, internally and externally, as required
• Statistical training and/or coaching, where appropriate
• Authoring/co-authoring papers and supporting junior team members to publish
• Technical interviews of senior statistical hires
• Active contributor to the statistical community through industry association involvement, conferences, webinars, blogs etc

Required experience/skills:

General

• Excellent communication skills both internally and externally at all levels within the company
• Growth mindset
• Leadership experience with responsibilities including strategy, ideally at a departmental level

Technical

• MSc or PhD in Statistics
• Minimum of 15 years’ experience working across pharma and CRO
• Active contributor to the wider statistical community
• Led either technical statistical initiatives and/or been the program lead throughout compound lifecycle to submission/registration
• Regulatory interaction experience

If you would like to speak further on this role before applying, please contact us at [email protected]

We look forward to hearing from you!