Senior Clinical Trial Manager – Immuno-Oncology & Cell Therapy

AbelZeta; Washington, Baltimore (District of Columbia, MD); On-site; USD 120,000 - 170,000; Full time

Benefits offered by this job

Comprehensive benefits package

401(k) with company match

Paid holidays and leave

Job summary

AbelZeta is seeking a (Sr.) Clinical Trial Manager to lead and optimize multicenter, Phase 2/3 oncology trials from the Clinical Operations team. You will oversee site selection, recruitment, monitoring, data integrity, and vendor relationships, ensuring trials are compliant and on time.

You will manage budgets, timelines, and cross-functional collaborations with clinical, safety, biostatistics, translational research, and regulatory teams, with travel within the US.

Qualifications

• Masters degree with 6+ years clinical research experience.
• Experience with SOPs and best practices for clinical trials.
• Strong knowledge of regulatory requirements (GCP/ICH/FDA).

Responsibilities

• Lead cross-functional teams to execute clinical trials.
• Oversee site selection, patient recruitment, and monitoring to ensure protocol adherence.
• Manage trial budgets and timelines to deliver on schedule and within budget.
• Oversee vendor relationships and CRO performance.
• Support contract negotiations with vendors and clinical sites.
• Ensure regulatory compliance with Sponsor SOPs and FDA/ICH guidelines.

Skills

Leadership

Budget management

Vendor management

Cross-functional collaboration

Project management

Communication skills

GCP/ICH/FDA familiarity

Education

Masters degree in life sciences

Bachelor's degree in related field

Tools

EDC systems

eTMF platforms

Regulatory documentation tools

Job description

AbelZeta is seeking a (Sr.) Clinical Trial Manager to lead and optimize multicenter, Phase 2/3 oncology trials from the Clinical Operations team. You will oversee site selection, recruitment, monitoring, data integrity, and vendor relationships, ensuring trials are compliant and on time.

You will manage budgets, timelines, and cross-functional collaborations with clinical, safety, biostatistics, translational research, and regulatory teams, with travel within the US.