Director, Clinical Trial Delivery

Albus Health

. Serve as the primary client-facing lead for delivery of Albus’ technology in clinical trials .

Posted 10/23/2026full-timeOxford • United KingdomLeadWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive experience in project management and client delivery within clinical trials, with a strong focus on regulatory compliance, stakeholder coordination, and operational excellence. Proven ability to lead multi-region trial deployments and improve client satisfaction through effective communication and documentation.

Highest-signal resume keywords

Project ManagementClinical Trial ProcessesRegulatory Compliance (GCP)Stakeholder CoordinationDigital Health Technologies

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Project ManagementClinical Trial ProcessesRegulatory Compliance (GCP)Data HandlingRisk ManagementSOP DevelopmentContract ReviewData Transfer AgreementsOperational PlanningMulti-Stakeholder Relationship Management

Soft Skills

Organizational SkillsCommunication SkillsLeadershipProactive Problem SolvingAttention to Detail

Tools & Technologies

ETMFsCTMSDigital Health TechnologiesRegulated DevicesData Protection Standards

Industry Keywords

Clinical TrialsMedical TechnologyPharmaceutical IndustryGDPRHIPAARespiratory DiseaseDigital BiomarkersSleep Monitoring

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Serve as the primary client-facing lead for delivery of Albus’ technology in clinical trials
Own the full delivery lifecycle from protocol and contract review through project planning, ongoing project management and closure
Lead project management, including weekly client check-in meetings, milestone tracking, risk and action capture, escalation management and transparent progress reporting
Improve and develop SOPs for client delivery
Contribute to pre-sales discussions with strategic and operational input to proposals and partnership development
Review MSAs, SOWs and contracts to extract delivery obligations and translate them into operational plans and timelines
Coordinate internal and external stakeholders across operations, technical support, data delivery, business development, QARA and senior management
Coordinate with CRAs and sites for materials preparation, training delivery and ongoing operational support
Ensure timely provision of regulatory and quality documentation
Manage study-specific data transfer agreements and coordinate secure data delivery to clients
Ensure smooth trial closeout, including final data delivery, hardware return, debriefs and lessons learned
Maintain detailed and traceable study documentation in compliance with internal SOPs and GCP
Work cross-functionally across operations, data, quality, product and clinical teams
Drive continuous improvement in operational processes, documentation and client satisfaction

Requirements

What you’ll need

7+ years of experience with medical technology or services in clinical trials
Preferably 3+ years with digital health technologies or within a small and rapidly growing team
10+ years of experience in project management or client delivery roles
Demonstrated leadership of several multi-region end-to-end trial deployments in sponsor-facing roles
Advanced and operational understanding of clinical trial processes, pharmaceutical industry requirements and regulatory standards (GCP)
Working knowledge of data and health standards, including data protection, GDPR and HIPAA
Demonstrated success managing multi-stakeholder client relationships
Excellent organizational and project management skills, with attention to detail
Strong written and verbal communication, especially for client and regulatory documentation
Independent, resourceful and proactive, comfortable owning projects end-to-end and working with varying degrees of seniority
Experience delivering regulated devices or software in trials, such as Class I/II devices, CE/FDA or SaMD
Understanding of data handling, security and compliance requirements, such as GDPR and HIPAA
Familiarity with trial documentation platforms, eTMFs or CTMS
Experience in respiratory disease, digital biomarkers or sleep monitoring domains

Benefits

Comp & perks

Stock Option Plan
Pension Plan
Training & Development
Cycle To Work Scheme
Exceptional growth opportunities in a rapidly growing startup
Equity options
Benefits