Clinical Research Associate- Oncology Monitoring Experience Required
Company: Ladders Agency
- Location: United States
- Work mode: Remote
- Employment type: Full-time
- Posted: 15 days ago
- Offer language: English
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. We encourage you to apply even if you don’t meet every qualification—your background could be exactly what this team needs.
