Clinical Study Manager

Ladders; United States; Remote; USD 110,000 - 130,000; Full time

Benefits offered by this job

Healthcare coverage

Retirement plans

Life insurance

Disability coverage

Employee assistance program

Training programs

Job summary

Ladders is seeking a Clinical Study Manager to oversee planning, execution, and monitoring of clinical studies for a US-based remote team. This role demands leadership in trial delivery with emphasis on quality and regulatory compliance.

You will partner with cross-functional stakeholders to coordinate timelines, budgets, resources, and issue resolution across the study lifecycle, ensuring data integrity and effective collaboration across scientific and operational teams.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Proven experience in clinical study management.
• Strong understanding of the drug development process and regulatory requirements.
• Excellent project management skills.
• Strong communication and interpersonal skills.
• Detail-oriented with a focus on data accuracy.

Responsibilities

• Oversee planning, execution, and monitoring of clinical trials.
• Collaborate with cross-functional teams to implement clinical studies.
• Develop and manage study budgets, resources, and timelines.
• Lead resolution of issues during clinical trials.
• Ensure data integrity and quality through monitoring processes.

Skills

Clinical study management

Project management

Communication skills

Data accuracy

Regulatory knowledge

Education

Bachelor's degree in a relevant scientific discipline or healthcare-related field

Job description

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

This role will oversee the planning, execution, and monitoring of clinical studies, ensuring trials are delivered with strong quality, compliance, and operational discipline. You will partner closely with cross-functional stakeholders to coordinate timelines, budgets, resources, and issue resolution across the study lifecycle. The position requires a detail-oriented leader who can help maintain data integrity while supporting effective collaboration across scientific and operational teams.

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

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

Responsibilities

• Oversee planning, execution, and monitoring of clinical trials
• Collaborate with cross-functional teams to implement clinical studies
• Develop and manage study budgets, resources, and timelines
• Lead resolution of issues during clinical trials
• Ensure data integrity and quality through monitoring processes

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• Proven experience in clinical study management
• Strong understanding of the drug development process and regulatory requirements
• Excellent project management skills
• Strong communication and interpersonal skills
• Detail-oriented with a focus on data accuracy

Benefits

• Competitive base salary and performance-related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training

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.