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UBC

Clinical Research Project Director

UBC

Project Director responsible for project operations and client relationship management at UBC. Leading teams in the delivery of clinical research projects.

Posted 7/14/2026full-timeRemote • 🇬🇧 United KingdomLeadWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates extensive experience in clinical research operations and project management, with a strong focus on financial oversight, quality control, and client satisfaction. Proven ability to lead cross-functional teams and drive operational strategies for global evidence development programs.

Highest-signal resume keywords
Clinical Research Operations ExperienceProject Management LeadershipFinancial Acumen and Budget ManagementICH GCP KnowledgeCross-Functional Team Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Project ManagementClinical Drug DevelopmentEvidence Development ProjectsProposal DevelopmentBudget DevelopmentData ManagementStatisticsMedical WritingRisk ManagementQuality Control
Soft Skills
LeadershipCommunicationNegotiationProblem-SolvingTime Management
Tools & Technologies
Project Management SoftwareMS Office
Industry Keywords
CROPharmaceuticalBiotechnologyClinical TrialsRegulatory CompliancePatient SafetyTherapeutic ExperiencePhase IV StudiesRWEExpanded Access Programs

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Provide strategic leadership, vision, and support to the project teams, ensuring alignment with the company's goals and client expectations.
  • Drive PM performance, project quality delivery, milestone timeline adherence, financial margin optimization, and customer satisfaction through efficient and effective directorship.
  • Ensure project teams prepare project plans to meet contracted services and timelines.
  • Lead and mentor multidisciplinary project teams, ensuring effective communication, collaboration, and performance of project deliverables according to contract terms.
  • Select, contract, and manage external vendors and subcontractors, when necessary, while maintaining quality and cost-effectiveness.
  • Monitor delivery of projects per scope and budgets.
  • Demonstrate strong oversight of financial health for assigned projects.
  • Proactive, ongoing identification of project risks and development of mitigating strategies.
  • Serve as the UBC senior operational contact with clients for all project related items.
  • Implement quality control measures to maintain the highest standards of data integrity, patient safety, and protocol compliance.
  • Prepare, maintain, and deliver high quality project progress reports, metrics, and other outputs to clients and UBC senior management.

Requirements

What you’ll need
  • Bachelor's degree in an appropriate discipline (Life Sciences, Healthcare, or Business) or equivalent industry experience
  • Advanced degree (Master's or Ph.D.) preferred.
  • Minimum 12 – 15 years of clinical research operations experience within a CRO, pharmaceutical, device/diagnostics or biotechnology company.
  • Minimum 10 years of experience at increasing levels of project management or clinical research oversight responsibilities.
  • Previous history as a Project Director or Director of Clinical Operations (related) within a CRO preferred.
  • Minimum 5 years supervisory/management experience.
  • Proven ability to lead, motivate, and manage cross-functional teams.
  • Strong understanding and experience in operational clinical operations and overall drug/biologic development processes.
  • Strong knowledge of functional components of clinical drug development (e.g., clinical, data management, statistics and medical writing).
  • Comprehensive knowledge of ICH GCP and applicable international regulations (EU Clinical Trials Directives, FDA Guidelines, etc.).
  • Broad therapeutic experience a plus.
  • Excellent understanding of and experience managing evidence development projects (e.g., Phase IV studies, RWE, Ph II – III clinical trials, expanded access programs, etc.) globally.
  • Ability to drive operational strategy for global evidence development programs.
  • Experience with proposal and budget development for evidence development programs.
  • Client focused with strong leadership skills.
  • Strong verbal, written, and interpersonal communication skills.
  • Strong prioritization, time management, and project management skills.
  • Strong negotiation, influencing, consensus building, and relationship management skills.
  • Strong innovative, analytical, problem-solving and decision-making skills.
  • Strong financial acumen and budget management experience.
  • Strong computer skills including MS Office.
  • Proficiency in project management tools and software.
  • Results driven and team-oriented, with the ability to influence outcomes as necessary.
  • Demonstrated ability to manage staff to achieve company and client goals.
  • Ability to handle multiple tasks in a fast-paced, deadline-oriented environment.
  • 10% travel availability.

Benefits

Comp & perks
  • Health solutions empowerment
  • Inclusive workplace fostering creativity
  • Project leadership
  • Team productivity and management
  • Risk management
  • Financial oversight
  • Quality compliance oversight
  • Business development assistance
  • Department administration and compliance oversight