Senior Clinical Trial Manager (CTM)

Ladders; United States; A distancia; USD 168.000 - 188.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Remote work flexibility

Occasional travel to Boston

Continuous improvement initiatives

Dynamic cross-functional teamwork

Industry-leading collaboration

Descripción de la vacante

Ladders is seeking a Senior Clinical Trial Manager to lead end-to-end trial delivery in the Pharmaceuticals & Biotech space. This remote role includes occasional travel to Boston and a strong emphasis on GCP compliance, TMF quality, and regulatory readiness.

You will partner with internal and external stakeholders, manage trial trackers and budgets, and drive continuous improvement across clinical development.

Formación

• 5+ years managing clinical trials in Sponsor or CRO environments.
• Deep understanding of clinical trial operations and international regulations.
• Proven experience leading clinical operations teams.
• Ability to collaborate across diverse functional areas.

Responsabilidades

• Manage clinical trials from protocol concept to study report in compliance with GCP and regulations.
• Engage strategically with key stakeholders.
• Oversee trial trackers for regulatory documents and study budget.
• Contribute to IRB/EC and regulatory submissions.
• Ensure TMF completeness and inspection readiness.
• Review documentation for quality requirements.
• Identify study risks and implement mitigation strategies.

Conocimientos

Trial management experience

Regulatory knowledge

Leadership

Cross-functional collaboration

Educación

Bachelor's degree in a scientific field

Advanced degree preferred

Descripción del empleo

For our client, we are seeking a Senior Clinical Trial Manager (CTM) to join the team of a leader in the Pharmaceuticals & Biotech space.

This role will lead the end-to-end management of clinical trials, from protocol concept through final study report, with a strong focus on compliance, quality, and operational execution. You will partner closely with internal and external stakeholders to keep studies on track, support regulatory readiness, and ensure trial documentation remains complete and inspection-ready. The position offers broad cross-functional exposure and the opportunity to influence study quality practices and continuous improvement across clinical development.

Location: Remote

Compensation: $168,000 – $188,000 annually

Responsibilities

• Manage clinical trials from protocol concept to study report while adhering to GCP and applicable regulations
• Engage strategically with key stakeholders
• Oversee clinical trial trackers for regulatory documents and study budget
• Contribute to IRB/EC and regulatory submissions
• Ensure TMF completeness and inspection readiness
• Review documentation for compliance with quality requirements
• Identify study risks and implement mitigation strategies

Qualifications

• Bachelor's degree in a scientific field; advanced degree preferred
• 5+ years managing clinical trials in a Sponsor or CRO environment
• Deep understanding of clinical trial operations and international regulations
• Proven experience leading clinical operations teams
• Ability to collaborate across diverse functional areas

Benefits

• Remote work flexibility with occasional travel to Boston
• Opportunities for continuous improvement initiatives in clinical development
• Work in a dynamic team environment across multiple functions
• Engagement with innovative research approaches
• Direct influence on quality practices and procedures in clinical trials

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.