Clinical Study Specialist (Biotechnology)

Location: Uxbridge, United Kingdom (Hybrid)

Company

hirify.global is a biotechnology company that develops and commercializes medicines for serious diseases through science-driven clinical research and innovation.

What you will do

• Deliver analysable study reports and performance metrics to the Clinical Study Lead.
• Coordinate study meetings, agendas, presentations, minutes, training materials, and investigator meetings.
• Collect feasibility and site-selection data, including site usability database reviews.
• Manage document reviews and maintain version-controlled regulatory, pharmacy, and laboratory manuals.
• Track site activation, enrollment, monitoring visits, registry postings, compliance reports, and Trial Master File close-out activities.
• Maintain SharePoint sites, site contacts, BDRM line listings, and third-party vendor oversight while escalating delays and recommending process improvements.

Requirements

• Bachelor's degree or five years of relevant experience.
• At least two years of industry-related experience.
• Experience supporting clinical trial execution and study documentation.
• Ability to coordinate with clinical study teams, sites, and third-party vendors.

Nice to have

• Advanced related degree.
• One to two years of relevant experience with an advanced related degree.

Culture & Benefits

• Inclusive workplace committed to equal opportunity and reasonable accommodation.
• Competitive total rewards package that may include bonuses, equity awards, pension or retirement benefits, insurance, paid time off, and family support benefits.
• Many roles emphasize working together onsite, with expectations discussed with the recruiter and hiring manager.