Remote Senior CRA - Phase I Oncology Trials

Ladders; United States; Remote; USD 111,000 - 138,000; Full time

Benefits offered by this job

Health and wellbeing

Retirement and pension plans

Life insurance

Disability coverage

Employee assistance programmes

Training and development

Job summary

Ladders is seeking a Senior CRA for Phase I Oncology trials, primarily remote within the United States, with important travel to sites across NJ/NY. You will monitor early‑phase oncology studies, ensuring adherence to protocols and regulatory standards while collaborating with cross‑functional teams to drive timely data collection and issue resolution.

You will guide sites and other CRAs, manage multiple sites and projects, and build strong relationships with site personnel to ensure quality

Qualifications

• Bachelor's degree in a scientific or healthcare-related field.
• Extensive experience as a Clinical Research Associate.
• Strong understanding of clinical trial processes and regulatory requirements.
• Proven ability to manage multiple sites and projects.
• Expertise in monitoring practices and site management.
• Excellent communication and interpersonal skills.
• Willingness to travel approximately 60%.

Responsibilities

• Oversee clinical trial site monitoring for protocol adherence
• Conduct site visits for performance assessment and issue resolution
• Collaborate with cross-functional teams for data collection and reporting
• Provide training and guidance to site staff and CRAs
• Build and maintain effective relationships with site personnel

Skills

CRAs experience

Multi-site management

Clinical trial processes

Regulatory knowledge

Communication skills

Travel willingness

Education

Bachelor's degree in a scientific or healthcare-related field

Job description

Ladders is seeking a Senior CRA for Phase I Oncology trials, primarily remote within the United States, with important travel to sites across NJ/NY. You will monitor early‑phase oncology studies, ensuring adherence to protocols and regulatory standards while collaborating with cross‑functional teams to drive timely data collection and issue resolution.

You will guide sites and other CRAs, manage multiple sites and projects, and build strong relationships with site personnel to ensure quality