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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing global clinical trials, ensuring compliance with ICH-GCP(R2) and regulatory standards while effectively leading cross-functional teams and overseeing vendor relationships. Strong financial acumen and analytical skills are essential for successful project execution and risk management.
Highest-signal resume keywords
Clinical Project ManagementOncology Program OversightICH-GCP(R2) ComplianceFull-Service Clinical Trial Lifecycle ManagementVendor Management
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Project ManagementDrug DevelopmentClinical ResearchRegulatory StandardsData Privacy PracticesFinancial AcumenAnalytical SkillsOperational Complexities ManagementTrial Master File ManagementStudy Record Management
Soft Skills
LeadershipCommunicationProblem-SolvingCollaborationAdministrative Excellence
Industry Keywords
Clinical TrialsGCPSOPsRisk ManagementResource AllocationStudy Start-UpMaintenanceClose-OutVendor OversightGlobal Study Execution
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
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 the unique operational complexities associated with Oncology 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
- Demonstrates 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