Senior Clinical Project Manager

Ladders; États-Unis; À distance; USD 120 000 - 145 000; Plein temps

Avantages offerts par ce poste

Competitive salaries

Annual performance-based bonuses

Equity-based incentive program

Generous vacation and paid wellness

Support for learning and development

Résumé du poste

Ladders is seeking a Senior Clinical Project Manager to oversee late-stage clinical trial programs from protocol finalization through study closeout. This remote role emphasizes execution, budget management, and cross-functional coordination with internal stakeholders, external partners, and leadership to keep studies on track.

Responsibilities include recruitment planning, vendor oversight, process improvements, and effective risk management, with opportunities for professional growth within a

Qualifications

• Bachelor's degree in life sciences required; PMP preferred.

Responsabilités

• Proactively manage all aspects of the trial process from protocol finalization to study closeout.
• Forecast and identify opportunities to accelerate activities and manage budgets.
• Independently develop integrated study management plans with the core project team.
• Monitor work performed by external partners to ensure quality and adherence to timelines.
• Manage risks proactively and lead problem-solving efforts.
• Develop patient recruitment strategies and conduct contract negotiations.
• Communicate trial status and issues to leadership and cross-functional stakeholders.

Connaissances

Budget management

Leadership

Cross-functional coordination

Risk management

Formation

Bachelor's degree in life sciences

PMP

Description du poste

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

This role will oversee late-stage clinical trial programs from protocol finalization through study closeout, with a strong focus on execution, budget management, and cross-functional coordination. You will work closely with internal stakeholders, external partners, and leadership to keep studies on track, mitigate risks, and drive high-quality outcomes. The position also calls for thoughtful planning around patient recruitment, vendor oversight, and process improvements across complex clinical development activities.

Location: Remote

Compensation: $120,000 – $145,000 annually

Responsibilities

• Proactively manage all aspects of the trial process from protocol finalization to study closeout
• Forecast and identify opportunities to accelerate activities and manage budgets
• Independently develop integrated study management plans with the core project team
• Monitor work performed by external partners to ensure quality and adherence to timelines
• Manage risks proactively and lead problem-solving efforts
• Develop patient recruitment strategies and conduct contract negotiations
• Communicate trial status and issues to leadership and cross-functional stakeholders

Qualifications

• Bachelor's degree in life sciences required; PMP preferred
• 5+ years of relevant experience in Clinical Trial Project Management
• Experience with late phase clinical trials (Phase 3 - 4), oncology, and/or radiopharmaceuticals preferred
• Thorough knowledge of ICH Good Clinical Practice (GCP) and regulatory processes
• Demonstrated leadership skills and ability to cultivate development of others

Benefits

• Competitive salaries
• Annual performance-based bonuses
• Equity-based incentive program
• Generous vacation and paid wellness days
• Support for learning and development opportunities

Our client is an equal opportunity employer.