Clinical Trial Manager, Senior – Oncology
Boehringer Ingelheim
Posted: 10/20/2026Google Cloud Platform
Clinical Trial Manager
Iovance Biotherapeutics, Inc.
Posted: 10/20/2026
Clinical Research Project Manager – Hybrid
University of Pennsylvania Perelman School of Medicine
Posted: 10/20/2026
Clinical Research Project Manager – A-B
Penn Information Systems & Computing
Posted: 10/20/2026
Clinical Research Associate
ICON plc
Posted: 10/20/2026
Clinical Research Associate
Syneos Health
Posted: 10/20/2026Senior Clinical Research Associate
ICON plc
Posted: 10/20/2026
Clinical Research Associate – Sponsor Dedicated
IQVIA
Posted: 10/20/2026
Senior Clinical Research Associate – Psychiatry
Worldwide Clinical Trials
Posted: 10/20/2026
Clinical Research Nurse – Home Visits
WEP Clinical
Posted: 10/20/2026Clinical Research Nurse – Home Visits, PRN
WEP Clinical
Posted: 10/20/2026Clinical Research Nurse – Home Visits
WEP Clinical
Posted: 10/20/2026Clinical Research Nurse – Home Visits
WEP Clinical
Posted: 10/20/2026Clinical Research Nurse, Home Visits
WEP Clinical
Posted: 10/20/2026
Associate Principal Scientist, Clinical Research
MSD
Posted: 10/20/2026Google Cloud Platform
Biostatistician II
Thermo Fisher Scientific
Posted: 10/20/2026D
Senior Biostatistician
DefinedTalent
Posted: 10/20/2026
Clinical Research Regulatory Specialist
Alcanza Clinical Research
Posted: 10/20/2026Google Cloud Platform
Senior Clinical Research Associate – CNS, Psychiatry
Worldwide Clinical Trials
Posted: 10/19/2026Senior Clinical Research Associate
ICON plc
Posted: 10/19/2026Clinical Trial Manager, Senior – Oncology
Boehringer IngelheimCore Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing late-phase Oncology clinical trials, ensuring compliance with GCP-ICH regulations, and effectively leading cross-functional teams. Proven ability to oversee trial budgets, patient engagement, and stakeholder communication while navigating complex trial environments.
Highest-signal resume keywords
Oncology Clinical Trials ManagementGCP-ICH ComplianceCross-Functional LeadershipClinical Trial Budget ManagementStakeholder Communication
Tech Stack
Tools & technologiesAbout the role
Key responsibilities & impact- Provide operational and scientific oversight for assigned late-phase Oncology clinical trials at regional/local level
- Plan, set up, execute, track, and deliver clinical trials according to milestones and KPIs
- Lead and direct the US trial team and communicate trial status to stakeholders
- Manage patient and site engagement, stakeholder communication, and trial team interactions
- Liaise with the Clinical Trial Leader on study-related issues
- Oversee compliance with GCP-ICH, regulations, SOPs, and trial protocols
- Create, manage, and review trial budgets
- Coordinate trial-specific training, feasibility, site selection, engagement plans, recruitment planning, and risk mitigation
- Coordinate patient-facing documents and report patient/site feedback to improve trial design
- Oversee vendor outsourcing and responses to regulatory authorities and ethics committees
- Monitor recruitment endpoints, clinical quality, safety reporting, and trial risks
- Support investigator meetings and maintain relationships with experts, sites, Patient Organizations, and stakeholders
- Ensure timely data cleaning, TMF archiving, CTR submissions, and communication of trial results
Requirements
What you’ll need- Bachelor's degree in life sciences or related field plus 6 years of clinical research experience, OR master's degree or PharmD plus 4 years, OR PharmD plus completion of a 2-year clinical research fellowship, OR PhD or MD plus 2 years
- For Senior Clinical Trial Manager: bachelor's degree in Life Sciences or related area plus 10 years of clinical research experience, master's degree or PharmD plus 8 years, OR PhD or MD plus 5 years
- Experience leading Oncology trials
- Skills in complex cross-functional matrix structures
- Scientific and therapeutic knowledge and operational expertise across clinical trial planning, execution and complexity
- Leadership and influential behaviors supporting, connecting and empowering teams
- Strategic and visionary thinking; ability to navigate ambiguity
- Ability to integrate study strategy with overall therapeutic area portfolio
- Ability to set priorities, manage pace, and use resources efficiently
- Ability to plan, define actions, resolve challenges, and translate learnings to new projects
- Ability and willingness to travel domestically and internationally 10–20% of the time
- Must be legally authorized to work in the United States without restriction
- Must be willing to take a drug test and post-offer physical if required
- Must be 18 years of age or older
Benefits
Comp & perks- Medical, dental and vision coverage
- Retirement savings opportunities
- Paid time off
- Paid holidays
- Disability and life insurance benefits
- Other company-sponsored programs
- Role-specific discretionary bonus eligibility
- Relocation eligibility
- International collaboration opportunities
- Work-life balance support
- Mobility and networking opportunities
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 PlanningTrial ExecutionData CleaningRisk MitigationPatient RecruitmentTrial Protocol OversightFeasibility AssessmentSafety ReportingTMF ArchivingCTR Submissions
Soft Skills
LeadershipStrategic ThinkingInfluential BehaviorsProblem SolvingTeam Empowerment
Industry Keywords
Life SciencesClinical ResearchRegulatory CompliancePatient OrganizationsEthics Committees