Clinical Team Manager/Sr. (CTM) - FSP

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

Benefits offered by this job

Competitive remuneration

Healthcare coverage

Career development

Innovative culture

Wellbeing

Job summary

Ladders is seeking a Clinical Team Manager/Sr. (CTM) - FSP to join our team in the Pharmaceuticals & Biotech space.

This remote role will oversee clinical monitoring operations and help drive study execution within a fast-paced environment, coordinating with internal stakeholders and sponsor partners to ensure quality, compliance and timely delivery. The position requires a Bachelor's degree with at least 5 years of relevant experience, strong ICH/GCP and FDA guidelines knowledge, and a

Qualifications

• Bachelor's degree with 5+ years of relevant experience.
• Strong understanding of ICH/GCP and FDA guidelines.
• Client-dedicated experience preferred.

Responsibilities

• Manage monitoring operations and ensure regulatory compliance.
• Develop clinical tools and study plans with sponsor stakeholders.
• Ensure timely deliverables and coordinate start-up activities.
• Conduct site visits and monitor trial progress.
• Identify and report site performance issues and trends.

Skills

Monitoring operations

ICH/GCP knowledge

FDA guidelines

Education

Bachelor's degree

Job description

For our client, we are seeking a Clinical Team Manager/Sr. (CTM) - FSP to join the team of a leader in the Pharmaceuticals & Biotech space.

This remote role will oversee clinical monitoring operations and help drive study execution within a fast-paced pharmaceutical environment. The position requires close coordination with internal stakeholders and external sponsor partners to ensure quality, compliance, and timely delivery across assigned studies. The work will focus on monitoring activities, site performance oversight, and start-up support while maintaining strong alignment with regulatory expectations.

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

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

Responsibilities

• Manage monitoring operations and ensure compliance with regulations
• Develop clinical tools and study plans in collaboration with sponsor stakeholders
• Ensure timely deliverables and coordinate start-up activities
• Conduct trip report reviews and monitor trial progress
• Identify and report site performance issues and trends
• Perform accompanied site visits and attend sponsor meetings
• Generate monitoring plans and complete trip report annotations

Qualifications

• Bachelor's degree with 5+ years of relevant experience
• Preferred experience in monitoring or study management
• Extensive background in Neuroscience is a plus
• Client-dedicated experience preferred
• Strong understanding of ICH/GCP and FDA guidelines

Benefits

• Competitive remuneration and annual incentive plan bonus
• Comprehensive healthcare coverage
• Opportunities for career development and advancement
• Innovative and supportive company culture
• Commitment to employee health and wellbeing

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.