Immunology Clinical Trial Manager – Lead Global Studies

SAB; Miami Beach (FL); On-site; USD 120,000 - 180,000; Full time

Job summary

SAB Bio is seeking a Clinical Trial Manager to lead planning, execution and management of biotech/pharma trials. The CTM will coordinate cross-functional teams, maintain budgets and timelines, and ensure GCP compliance across global sites.

Strong leadership and communication skills are required, with travel up to 25% and preference for candidates in the ET zones. Responsibilities include protocol development support, trial master file maintenance, vendor oversight, and stakeholder reporting,

Qualifications

• B.S. degree with 6–8+ years of experience managing clinical trials.
• Experience managing global trials and CRO relationships.
• Experience with Phase II and III oversight and management.
• Strong timeline management and regulatory knowledge (FDA/EMA/MHRA).
• Proficiency with EDC, CTMS and eTMF systems.

Responsibilities

• Lead design and execution of trial protocols, site selection and patient recruitment.
• Oversee budget tracking, timelines and quality for trials.
• Coordinate cross-functional teams and CROs for trial delivery.
• Manage site relationships and vendor oversight, including invoice review.
• Prepare updates for stakeholders and oversee trial risk management.

Skills

Leadership

Communication

Multi-tasking

Problem solving

Regulatory compliance

Study execution

Timeline management

Team collaboration

Inspection readiness

Independent work

Education

Bachelor's degree in science

Tools

Veeva

Agatha

CTMS

eTMF

Smartsheet

MS Office

Job description

SAB Bio is seeking a Clinical Trial Manager to lead planning, execution and management of biotech/pharma trials. The CTM will coordinate cross-functional teams, maintain budgets and timelines, and ensure GCP compliance across global sites.

Strong leadership and communication skills are required, with travel up to 25% and preference for candidates in the ET zones. Responsibilities include protocol development support, trial master file maintenance, vendor oversight, and stakeholder reporting,