Senior CRA- Phase I Oncology- NJ/NY

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

For our client, we are seeking a Senior CRA- Phase I Oncology- NJ/NY to join the team of a leader in the Pharmaceuticals & Biotech space.

This role will focus on monitoring early-phase oncology clinical trials, ensuring site activities align with study protocols, regulatory requirements, and quality standards.

The Senior CRA will partner closely with site personnel and cross-functional teams to support timely data collection, issue resolution, and efficient trial execution.

The position also involves providing guidance to sites and monitoring activities across a travel-heavy territory, with a strong emphasis on relationship management and operational oversight.

Location: Remote - US based candidates only, no visa sponsorship available

Compensation: $110,520 – $138,150 annually

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

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%

Benefits

• Comprehensive total rewards package
• Health and wellbeing programmes including medical, dental, and vision coverage
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes
• Learning and development opportunities through structured training

Our client is an equal opportunity employer. We encourage you to apply even if you don’t meet every qualification—your background could be exactly what this team needs.