Remote Clinical Trials Study Manager – Biosamples

ICON Clinical Research; City of Rome (NY); Hybrid; USD 95,000 - 150,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Retirement planning

Employee Assistance Programme

Life assurance

Flexible country-specific benefits

Job summary

ICON Strategic Solutions is seeking a Laboratory Study Manager sponsor-dedicated role in a remote setting across the EMEA region. The role focuses on coordinating clinical trial delivery, resolving issues, and building team capability, while ensuring regulatory compliance and high data quality.

The candidate will design and analyze trials, manage budgets and timelines, and collaborate with external partners to advance treatments that benefit patients worldwide.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Proven experience in clinical study management within drug development.
• Strong project management skills with ability to multitask.
• Excellent communication and stakeholder management abilities.
• Detail-oriented with focus on data accuracy and quality.

Responsibilities

• Oversee planning, execution, and monitoring of clinical trials to meet timelines and regulatory requirements.
• Collaborate with investigators, vendors, and internal teams to drive study success.
• Develop and manage study budgets, resources, and timelines for efficient operations.
• Lead issue resolution and risk management throughout the study lifecycle.
• Ensure data integrity and quality through rigorous monitoring and validation.

Skills

Project management

Communication

Cross-functional collaboration

Attention to detail

Education

Bachelor's degree in a scientific/healthcare field

Job description

ICON Strategic Solutions is seeking a Laboratory Study Manager sponsor-dedicated role in a remote setting across the EMEA region. The role focuses on coordinating clinical trial delivery, resolving issues, and building team capability, while ensuring regulatory compliance and high data quality.

The candidate will design and analyze trials, manage budgets and timelines, and collaborate with external partners to advance treatments that benefit patients worldwide.