Clinical Trial Manager (Oncology)
Remote (U.S.) | Contract Opportunity
Overview A growing research-focused life sciences organization is seeking an experienced Clinical Trial Manager to oversee the operational execution of early-stage oncology studies. This individual will play a key role in driving study timelines, managing external partners, and ensuring high-quality trial conduct from startup through closeout.
Responsibilities
Lead and support clinical study startup, activation, and ongoing execution activities.
Oversee study progress, enrollment metrics, and operational deliverables across multiple sites.
Conduct review of study data, monitoring visit reports, and key trial documentation to ensure quality and compliance.
Partner with vendors, CROs, and cross-functional stakeholders to track performance and study milestones.
Identify operational risks, develop mitigation strategies, and resolve study-related issues proactively.
Ensure Trial Master File (TMF) documentation remains inspection-ready and compliant.
Provide regular study updates, reports, and communications to project leadership.
Support process improvement initiatives and other clinical operations activities as needed.
Qualifications
Bachelor's degree in a life sciences or related discipline.
Significant clinical operations experience within the pharmaceutical, biotechnology, or research industry.
Demonstrated success managing oncology clinical trials, including early-phase studies.
Experience overseeing CROs and external vendors.
Strong understanding of clinical trial startup, site management, and study execution.
Knowledge of GCP, ICH guidelines, and applicable regulatory requirements.
Excellent communication, organizational, and problem-solving skills.
Proficiency with Microsoft Office and clinical trial management systems.
International startup experience is a plus.
Preferred Experience
Management of Phase I and/or Phase II oncology studies.
Experience working in fast-paced, collaborative clinical development environments.
Ability to independently manage competing priorities and drive studies forward.
Work Arrangement
Fully remote within the United States.
Contract engagement with potential for extension based on project needs.
This opportunity is ideal for a clinical operations professional who enjoys working in a hands-on role supporting innovative oncology development programs while collaborating with cross-functional teams and external partners.