Remote Regional Clinical Study Leader

Ladders; United States; Remote; USD 136,000 - 181,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) with company match

FSA/HSA

Life insurance

Paid time off

Employee stock purchase plan

Equity awards discretionary

Job summary

Ladders is seeking a Regional Clinical Study Manager to lead the regional clinical operations team in a remote US-based setting. You will drive study delivery, ensure alignment with study goals, and oversee timelines and feasibility across the region.

The role requires 6+ years in clinical research, strong leadership, and ICH/GCP knowledge. You will collaborate with cross-functional teams to support regulatory submissions, vendor management, and ongoing inspection readiness while advancing the

Qualifications

• 6+ years of clinical research experience in biotech, pharma, or a CRO.
• Proven leadership experience in clinical functions.
• Bachelor’s degree in a scientific or healthcare discipline; higher degree preferred.
• Strong knowledge of ICH/GCP regulations and clinical trial processes.

Responsibilities

• Lead the regional clinical operations team and manage study delivery.
• Ensure alignment of regional deliverables with overall study goals.
• Manage study timelines and ensure operational feasibility in the region.
• Collaborate with stakeholders to support timely regulatory submissions.
• Monitor compliance with study protocols and maintain inspection readiness.
• Manage regional study budgets and vendor relationships.
• Provide mentorship and performance feedback to team members.

Skills

Leadership

Regulatory knowledge

Budget management

Cross-functional collaboration

Study delivery

Education

Bachelor's degree in a scientific/healthcare field

Job description

Ladders is seeking a Regional Clinical Study Manager to lead the regional clinical operations team in a remote US-based setting. You will drive study delivery, ensure alignment with study goals, and oversee timelines and feasibility across the region.

The role requires 6+ years in clinical research, strong leadership, and ICH/GCP knowledge. You will collaborate with cross-functional teams to support regulatory submissions, vendor management, and ongoing inspection readiness while advancing the