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Iovance Biotherapeutics, Inc.Posted 10/20/2026full-timeRemote • United StatesMid-LevelSenior💰 $145,000 - $165,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing clinical trials from inception to completion, including vendor selection, data integrity, and compliance with US and Global Regulations. Proficient in overseeing cross-functional teams and ensuring timely execution of clinical studies while maintaining budgetary constraints.
Highest-signal resume keywords
Clinical Trial ManagementVendor Selection and ManagementData Integrity and AnalysisRegulatory Compliance (ICH-GCP, FDA-CFR)Cross-Functional Team Leadership
About the role
Key responsibilities & impact- Support the operational execution of clinical studies across one or more clinical programs from initial study synopsis through final deliverables, including database hard-lock, final TLFs, and CSR
- Manage implementation, on-time execution, and conduct of clinical studies, including budgets, milestones, timelines, scope, resources, and vendor selection
- Oversee cross-functional study team members to ensure execution within approved budgets and timelines
- Manage and mitigate risks, prioritizing competing tasks and issues
- Lead vendor identification, qualification, and selection
- Set up and manage systems including EDC, IWRS, central laboratories, ePRO, and eDiary services
- Support trial endgame data and statistical analyses
- Assess data to detect trends and outliers and direct resources to resolve problems
- Review and supervise multifunctional vendor groups across clinical operations, data management, and biometrics
- Ensure data integrity through data reviews, query resolution, and consistency checks, including for independent DMC/DSC
- Track and communicate program and study progress to Senior Management using dashboards and trackers
- Assess competitive landscape, changing regulations, and guidance and modify clinical projects as necessary
- Approach challenges and problem resolution creatively to optimize clinical trial conduct
- Perform miscellaneous duties as assigned
Requirements
What you’ll need- Bachelor’s degree with 5+ years of pharmaceutical or biotech-related/clinical research, oncology or research experience and at least 1 year as CTM
- Demonstrated experience in core and technical aspects of designing, initiating and managing phase 1-4 clinical trials
- Demonstrated experience in management of CROs and vendor selection
- Excellent interpersonal and communication skills, with demonstrated leadership attributes
- Subject matter expertise in US and Global Regulations and Guidance, including SOPs, ICH-GCP, FDA-CFR, and ethical standards
- Broad scope experience in data collection, monitoring, cleaning and analysis throughout clinical development (Phase 1-4)
- Ability to remain in a stationary position standing or sitting for prolonged periods of time
- Ability to move about inside an office and exert up to 10 pounds of force occasionally or a negligible amount of force frequently or constantly
- Visual acuity for preparing and analyzing data and figures, viewing a computer screen, and extensive reading
- Ability to perform repetitive motion involving the wrists, hands, and/or fingers
- Ability to communicate with others to exchange information
- Clear and conceptual thinking ability; excellent judgment, troubleshooting, problem-solving, analysis, and discretion
- Ability to handle work-related stress, multiple priorities, and deadlines
- Must adhere to Iovance Biotherapeutics’ core values, policies, procedures, and business ethics
Benefits
Comp & perks- Equal-opportunity employer
- Reasonable accommodations available upon request
- Remote work environment
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 DesignData Collection and MonitoringStatistical AnalysisRisk ManagementBudget ManagementProject ManagementDatabase Hard-LockFinal TLFsCSR PreparationEDC Systems Management
Soft Skills
Interpersonal SkillsCommunication SkillsLeadership AttributesProblem-SolvingJudgment
Tools & Technologies
EDCIWRSEPROEDiary ServicesDashboards and Trackers
Industry Keywords
PharmaceuticalBiotechClinical ResearchOncologySOPsPhase 1-4 TrialsCRO ManagementData ManagementBiometricsEthical Standards