Clinical Research Associate- Oncology Monitoring Experience Required

Ladders; United States; Remote; USD 110,000 - 130,000; Full time

Job summary

Ladders is seeking a Clinical Research Associate- Oncology Monitoring with strong site oversight and ICH GCP compliance to join a leading pharma/biotech team. This remote US-based role emphasizes hands-on monitoring visits, protocol adherence, and cross-functional collaboration.

The candidate will work closely with study sites to drive high-quality execution across oncology programs, manage adverse event reporting, and ensure safety and regulatory requirements are met in a fast-paced environment.

Qualifications

• 2+ years of oncology monitoring experience.
• Knowledge of clinical research, ICH GCP and local regulations.

Responsibilities

• Provide guidance and oversight to the CRA team for project adherence.
• Conduct co-monitoring and evaluation visits as needed.
• Coordinate with cross-functional departments for issue resolution.
• Assist in developing study-specific Monitoring Plans and training presentations.
• Perform qualification, initiation, interim, and close-out visits with proper documentation.
• Maintain regular contact with study sites to ensure compliance and assess patient accrual rates.
• Facilitate adverse event reporting and ensure SAE reconciliation.

Skills

Oncology monitoring

ICH GCP knowledge

Regulatory compliance

Prioritization

Education

Bachelor's degree in Biology or Life Sciences

Job description

For our client, we are seeking a Clinical Research Associate- Oncology Monitoring Experience Required to join the team of a leader in the Pharmaceuticals & Biotech space.

This role will support oncology clinical trial monitoring activities, with a strong emphasis on site oversight, protocol adherence, and compliance with ICH GCP and local regulations. The position partners closely with study sites and cross-functional teams to help drive high-quality execution across diverse clinical research programs. It also includes hands‑on participation in monitoring visits, documentation, issue resolution, and safety reporting in a fast‑paced pharmaceutical and biotech environment.

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

Compensation: $110,000 - $130,000 annually

Responsibilities

• Provide guidance and oversight to the CRA team for project adherence
• Conduct co-monitoring and evaluation visits as needed
• Coordinate with cross-functional departments for issue resolution
• Assist in developing study‑specific Monitoring Plans and training presentations
• Perform qualification, initiation, interim, and close‑out visits, ensuring proper documentation
• Maintain regular contact with study sites to ensure compliance and assess patient accrual rates
• Facilitate adverse event reporting and ensure reconciliation of SAE reports

Qualifications

• 2+ years of oncology monitoring experience required
• Bachelor's degree in Biology or Life Sciences
• Strong command of the local language, both written and verbal
• Knowledge of clinical research, ICH GCP, and local regulations
• Proven ability to manage priorities and solve problems

Benefits

• Collaborative team environment with opportunities for mentoring
• Professional development through training and onboarding
• Exposure to diverse clinical trial projects
• Opportunity to work closely with cross-functional teams
• Supportive company culture focused on quality and compliance

Our client is an equal opportunity employer.