Clinical Trial Manager, Senior – Oncology

This is a fully remote position, open to applicants in United States.

📋 Description

• Provide scientific and operational oversight for late-phase Oncology clinical trials at the regional and local levels.

• Plan, initiate, execute, monitor, and deliver clinical trials in alignment with milestones and KPIs.

• Lead and guide the US trial team while communicating trial status updates to stakeholders.

• Manage patient and site engagement, facilitate stakeholder communication, and oversee trial team interactions.

• Collaborate with the Clinical Trial Leader on issues related to the study.

• Ensure compliance with GCP-ICH guidelines, relevant regulations, SOPs, and trial protocols.

• Develop, manage, and review trial budgets.

• Coordinate trial-specific training, site feasibility, selection, engagement strategies, recruitment planning, and risk management.

• Organize patient-facing documentation and relay patient/site feedback to enhance trial design.

• Supervise vendor outsourcing and handle communications with regulatory authorities and ethics committees.

• Monitor recruitment targets, 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 dissemination of trial results.

⛳️ Requirements

• Bachelor's degree in life sciences or a related field with a minimum of 6 years of clinical research experience, OR a master's degree or PharmD with at least 4 years, OR PharmD with completion of a 2-year clinical research fellowship, OR a PhD or MD with a minimum of 2 years.

• For the Senior Clinical Trial Manager position: a bachelor's degree in Life Sciences or a comparable field plus 10 years of clinical research experience, a master's degree or PharmD with at least 8 years, OR a PhD or MD with a minimum of 5 years.

• Proven experience in leading Oncology trials.

• Proficiency in managing complex cross-functional matrix structures.

• Possess scientific and therapeutic knowledge along with operational expertise in clinical trial planning, execution, and complexity.

• Demonstrated leadership and influential behaviors that support, connect, and empower teams.

• Strategic and visionary thinking skills; adept at navigating ambiguity.

• Ability to align study strategy with the broader therapeutic area portfolio.

• Competence in setting priorities, managing pace, and utilizing resources effectively.

• Capability to plan, define actions, resolve challenges, and apply learnings to new projects.

• Willingness and ability to travel domestically and internationally 10-20% of the time.

• Must be legally authorized to work in the United States without restrictions.

• Must be prepared to undergo drug testing and a post-offer physical examination if required.

• Must be at least 18 years of age.

🏝️ Benefits

• Medical, dental, and vision insurance coverage.

• Opportunities for retirement savings.

• Paid time off policies.

• Paid holidays.

• Disability and life insurance benefits.

• Additional company-sponsored programs.

• Eligibility for role-specific discretionary bonuses.

• Relocation assistance eligibility.

• Opportunities for international collaboration.

• Support for work-life balance.

• Mobility and networking opportunities.