Senior Clinical Project Manager

Location: United Kingdom; permanent remote opportunity with potential for hybrid work depending on location.

Company

hirify.global is a global full-service CRO providing clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies across more than 20 countries.

What you will do

• Lead and coordinate complex clinical projects in accordance with contracts, SOPs, ICH-GCP guidelines, and regulatory requirements.
• Manage sponsors, investigators, CRO services, clinical research associates, clinical research assistants, biometrics, safety, regulatory, and other cross-functional contributors.
• Plan and monitor project timelines, budgets, workload, team performance, documentation, and study-specific services.
• Coordinate regulatory approvals, study data and document management, archiving, monitoring activities, and investigator meetings.
• Support protocols, case report forms, clinical study reports, SOPs, project training, and technical activities.
• Provide sponsor updates, escalate issues, and mentor Project Coordinators and Project Manager I colleagues.

Requirements

• At least 8 years of clinical research project management experience.
• Previous CRO experience is required.
• Experience managing respiratory, rare disease, general medicine, and/or GLP-1 studies is required; complex clinical trial experience is expected.
• Bachelor’s degree or equivalent in a scientific, medical, paramedical, or nursing discipline.
• Strong knowledge of clinical trial operations, GCP/ICH guidelines, and applicable regulatory requirements.
• Fluent English is required. Proficiency in Microsoft Office is also required.

Nice to have

• Previous Clinical Research Associate or Clinical Monitor experience.
• Experience with electronic data capture systems.
• Experience as a Technical Specialist in a therapeutic or technical area.

Culture & Benefits

• Permanent remote work with potential for a hybrid arrangement depending on location.
• Collaborative, quality-driven one-team culture.
• Professional development, continuous training, and structured mentoring.
• Work supporting the development and commercialization of innovative medicines and medical devices.
• Inclusive and diverse workplace focused on improving global healthcare.

Hiring process

• Submit a CV and receive an application acknowledgement.
• Qualified candidates are invited to an initial phone interview.