Clinical Trials Program Lead – Stroke Platform

Mount Sinai; New York (NY); On-site; USD 105,000 - 157,000; Full time

Job summary

Mount Sinai Morningside is seeking a Clinical Trials Manager to oversee national project management for the STEP acute stroke platform trial. You will work directly with performance sites and lead cross-functional teams to ensure study milestones are met.

The ideal candidate has a clinical background with extensive trial experience, strong leadership, and a track record of regulatory diligence. This role requires coordinating study documents, training staff, and maintaining study protocols

Qualifications

• Bachelor's degree in nursing, biology, public health or related field; masters preferred.
• 6+ years managing clinical trials, with 2+ years in leadership; 9+ years preferred.
• Excellent communication, problem-solving, organizational and leadership skills.
• SOCRA and/or ACRP certification preferred.

Responsibilities

• Monitor and report trial progress including budgets and timelines.
• Prepare and review trial documents.
• Organize study meetings.
• Ensure resources for project execution.
• Develop training materials and train staff.
• Communicate study updates with sites.
• Lead the clinical project team and meetings.
• Maintain protocol versions and procedures manuals.
• Support regulatory compliance and safety reporting.

Skills

Communication skills

Leadership

Teamwork

Attention to detail

Problem-solving

Regulatory compliance

Education

Bachelor's degree in Nursing, Biology, and Public Health or related scientific/health field

Master's degree preferred

Tools

Basic computer applications

Clinical trial management software (CTMS)

Job description

Mount Sinai Morningside is seeking a Clinical Trials Manager to oversee national project management for the STEP acute stroke platform trial. You will work directly with performance sites and lead cross-functional teams to ensure study milestones are met.

The ideal candidate has a clinical background with extensive trial experience, strong leadership, and a track record of regulatory diligence. This role requires coordinating study documents, training staff, and maintaining study protocols