Clinical Team Manager / Sr. (CTM) - Neuro

Ladders; United States; A distancia; USD 110.000 - 130.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Standard Monday-Friday schedule

Office-based work environment with装备提供

Descripción de la vacante

Ladders is seeking a Clinical Team Manager / Senior (CTM) - Neuro for our client in the Pharmaceuticals & Biotech space. This remote US-based role oversees clinical operations and study quality across neuroscience programs, ensuring trials move forward in line with ICH GCP standards.

The CTM will partner with clinical teams, study sites, and internal stakeholders to drive startup activities, resolve issues, and meet milestones in a fast-paced CRO-like environment.

Formación

• Bachelor's degree or equivalent in a relevant field.
• 5+ years of experience in clinical research or trial operations.
• End-to-end study management experience is essential.
• Early Phase and start-up experience preferred.
• Neurology therapy expertise; ophthalmology and rare diseases experience favored.

Responsabilidades

• Manage clinical operations and quality for assigned studies in compliance with ICH GCP.
• Develop clinical tools and contribute to clinical-related document creation.
• Collaborate with clinical teams and lead meetings to ensure project deliverables are met.
• Monitor clinical activity timelines and metrics to ensure final deliverables are achieved.
• Communicate with study sites regarding protocol and study-related issues.
• Coordinate start-up activities and ensure regulatory submissions are addressed.
• Manage clinical resources and delegate responsibilities as necessary.

Conocimientos

End-to-end study management

Cross-functional coordination

Timeline management

Educación

Bachelor's degree in a relevant field

Descripción del empleo

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

This role will oversee clinical operations and study quality for assigned neuroscience programs, with responsibility for keeping trials moving in alignment with ICH GCP standards. The position partners closely with clinical teams, study sites, and internal stakeholders to drive start-up activities, resolve study issues, and support timely delivery of key milestones. It is well suited for someone with end-to-end study management experience who can balance operational execution, documentation, and cross-functional coordination in a fast-paced clinical research environment.

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

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

Responsibilities

• Manage clinical operations and quality for assigned studies in compliance with ICH GCP.
• Develop clinical tools and contribute to clinical-related document creation.
• Collaborate with clinical teams and lead meetings to ensure project deliverables are met.
• Monitor clinical activity timelines and metrics to ensure final deliverables are achieved.
• Communicate with study sites regarding protocol and study-related issues.
• Coordinate start-up activities and ensure regulatory submissions are addressed.
• Manage clinical resources and delegate responsibilities as necessary.

Qualifications

• Bachelor's degree or equivalent in a relevant field.
• 5+ years of experience in clinical research or trial operations.
• End-to-end study management experience is essential.
• Early Phase and start-up experience preferred.
• Therapeutic expertise in Neurology; experience with Ophthalmology and Rare Diseases is favored.

Benefits

• Standard Monday-Friday work schedule.
• Office-based work environment with equipment provided.
• Opportunities for professional development and training in clinical management.

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.