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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing clinical trials, ensuring compliance with GCP and regulatory standards, and overseeing cross-functional teams to deliver projects on time and within budget. Strong financial acumen and analytical skills are essential for effective project management in drug development.
Highest-signal resume keywords
Clinical Trial Project ManagementGCP ComplianceOncology Program ManagementVendor ManagementDrug Development Experience
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial ManagementProject PlanningRegulatory StandardsData Privacy PracticesFinancial AcumenAnalytical SkillsFull-Service Clinical Trial LifecycleOncology ExpertiseNeurology ExpertiseImmunology & Infectious Diseases Expertise
Soft Skills
LeadershipCommunicationProblem-SolvingCollaborationProactive Risk Management
Tools & Technologies
Trial Master FileStudy Records Management
Industry Keywords
GCPICH-GCP(R2)Cell & Gene TherapyClinical ResearchLife Science DegreeHealthcare DegreeBusiness Degree
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 strategically
- Proactively address challenges, scope changes, risks, and resource allocation
- Lead key meetings and ensure 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 to 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 5 years of experience in drug development and/or clinical research, with at least 2-3 years of clinical trial project management experience
- Strong expertise managing the unique operational complexities associated with Oncology, Neurology, and Immunology & Infectious Diseases programs, including oversight of specialized vendors, timelines, safety considerations, and global study execution
- Cell & Gene therapy is a plus
- 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