Project Manager II, Global Project Leadership

Allucent

. Lead cross-functional teams to deliver clinical trials on time, within scope, and on budget .

Posted 10/9/2026full-timeUnited StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical trials, ensuring compliance with GCP and regulatory standards, and effectively leading cross-functional teams to deliver projects on time and within budget. Proficient in overseeing the full-service clinical trial delivery lifecycle and managing specialized vendors in various therapeutic areas.

Highest-signal resume keywords

Clinical Project ManagementGCP ComplianceDrug Development ExperienceFinancial AcumenVendor Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Project ManagementClinical Trial DeliveryRegulatory StandardsData Privacy PracticesAnalytical SkillsLifecycle ManagementInfectious Disease ProgramsImmunology ProgramsCell & Gene TherapyNeurology Programs

Soft Skills

LeadershipCommunicationProblem-SolvingCollaborationAdministrative Excellence

Industry Keywords

ICH-GCP(R2)Clinical ResearchLife ScienceHealthcareRegulatory Requirements

About the role

Key responsibilities & impact

Lead cross-functional teams to deliver clinical trials on time, within scope, and on budget
Develop and execute project plans aligned with GCP, SOPs, and regulatory standards
Serve as the primary point of contact for sponsors, vendors, and internal teams
Select, manage, and oversee vendors
Proactively address challenges, scope changes, risks, and resource allocation
Lead key meetings and ensure the Trial Master File and study records are complete and inspection-ready
Drive global clinical trials from study start-up through final delivery
Oversee cross-functional teams and ensure studies remain on track, on budget, and compliant with GCP and regulatory requirements

Requirements

What you’ll need

Minimum Bachelor’s degree in life science, healthcare and/or business degree
Minimum 6 years of relevant work experience, specifically experience in drug development and/or clinical research
Minimum 1 year of project management experience, specifically as a clinical project manager
Strong expertise managing Infectious Disease, Immunology & Inflammation, Cell & Gene Therapy, and Neurology programs, including oversight of specialized vendors, timelines, safety considerations, and global study execution
Expert knowledge of ICH-GCP(R2), data and patient privacy practices, and applicable (local) regulatory requirements
Strong financial acumen, administrative excellence and analytical skills
Experience managing all phases of the full-service clinical trial delivery lifecycle (Start-up, Maintenance, Close-out)

Benefits

Comp & perks

Comprehensive benefits package per location
Competitive salaries per location
Departmental Study/Training Budget for furthering professional development
Flexible Working hours (within reason)
Opportunity for remote/hybrid* working depending on location
Leadership and mentoring opportunities
Participation in our enriching Buddy Program as a new or existing employee
Internal growth opportunities and career progression
Financially rewarding internal employee referral program
Access to online soft-skills and technical training via internal platforms
Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects
Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees