Regional Clinical Study Manager

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

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

This role will oversee regional clinical study execution and help ensure that study deliverables are completed on time, within scope, and in alignment with broader program goals. You will partner closely with cross-functional stakeholders to support regulatory readiness, protocol compliance, and operational feasibility across the region. The position also carries responsibility for team leadership, vendor coordination, and budget oversight in a highly regulated clinical development environment.

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

Compensation: $136,400 – $181,400 annually

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

Qualifications

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

Benefits

• Comprehensive medical, dental, and vision coverage
• 401(k) plan with company match
• Flexible spending accounts (FSA/HSA)
• Life insurance and wellness programs
• Paid time off
• Employee stock purchase plan
• Opportunity of discretionary equity awards

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.