Director, Clinical Study Management – Project Management

Alimentiv

. Provide leadership and oversight for global activities and timelines related to execution of full-service clinical trials .

Posted 11/2/2026full-timeRemote • United Kingdom, IrelandLead💰 £93,000 - £155,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive leadership in managing full-service clinical trials, with a strong focus on project management, financial oversight, and compliance within the CRO industry. Proven ability to develop strategies, manage resources, and ensure high-quality service delivery while meeting regulatory standards.

Highest-signal resume keywords

Full-Service Project ManagementCRO Industry ExperienceBudget Setting and Financial OversightGastrointestinal Clinical Trial ManagementRegulatory Compliance Monitoring

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Project ManagementBudget PreparationFinancial ReportingRisk ManagementPolicy DevelopmentOperational PlanningResource ManagementIssue ResolutionChange-Order DevelopmentStaff Performance Management

Soft Skills

LeadershipCoachingCommunicationCustomer ServiceTeam Development

Industry Keywords

Clinical TrialsPhase II ExperiencePhase III ExperienceGastrointestinal TrialsBest PracticesRegulatory StandardsOperational ReviewsBid DevelopmentClient MeetingsCross-Department Planning

About the role

Key responsibilities & impact

Provide leadership and oversight for global activities and timelines related to execution of full-service clinical trials
Oversee project management and project finance teams
Participate in developing and implementing organizational strategies, technologies and best practices
Support customer service, staff development, information management reporting, and divisional short- and long-term goals
Develop and improve policies and processes
Oversee product quality and compliance monitoring
Plan staff resources and manage staff and contractor performance
Represent project and finance teams with sponsors and clients throughout the project life cycle
Ensure high-quality, timely service delivery in accordance with corporate and industry best practices and regulatory requirements
Support Business Development through bid development and bid defenses
Participate in operational planning and establish measurable goals and targets
Oversee project development, resource and financial requirements, trial conduct, confidentiality, and issue resolution
Ensure sufficient project staffing and maintain utilization targets
Represent project operations in cross-department planning initiatives, client meetings, business development meetings, bid defenses, scientific conferences, and investigator meetings
Evaluate and implement recommendations to minimize organizational risk and meet regulatory or industry standards
Plan, manage, advocate, and report on department budgets and annual operational reviews
Monitor financial and regulatory risks and direct risk-management methodologies
Prepare budgets and proposal text for RFPs, RFIs, and statements of work
Oversee change-order development for full-service projects

Requirements

What you’ll need

Undergraduate university degree (Bachelor or Honors Bachelor) plus minimum of 10 years related experience and training/continuous ongoing development OR college diploma/degree and a minimum of 15 years related experience
Deep experience in CRO industry with full-service project management leadership, coaching and leading a team with an excellence mindset
Phase II experience prerequisite
Phase III experience highly desirable
Experience in gastrointestinal (GI) clinical trial project management highly desirable
Significant financial responsibility, including extensive participation in budget setting, autonomous expenditure and/or revenue generation decisions limited by company policy or financial processing, reconciliation and reporting
Resumes must be submitted in English

Benefits

Comp & perks

Annual Bonus target
Education Reimbursement program for full-time employees
Monthly Cell Phone and Remote Work Allowance (dependent on role eligibility)
One time office setup allowance (can be used to purchase a scanner/printer, extra monitor, office furniture, etc.)
Working while visiting program – up to 4 weeks per year!
Flexible Summer Hours Program from May – September
Employee referral incentive
Full-time employees also become beneficiaries of the Alimentiv Trust after one year of employment, and permanent members after 5 years of employment
Optional formal mentorship program (Alimentorship)
Country/region annual social events in person
Leadership development programs for people leaders in accordance with your seniority
Social committee and several other optional initiatives designed to support you in feeling like part of the Alimentiv team
Additional benefits may be available depending on the country of employment and are subject to local policies and eligibility.