Remote Clinical Trial Manager, Biotech Leader

ICON Clinical Research; Center Square (PA); Remote; USD 110,000 - 140,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Employee Assistance Programme LifeWorK

Life assurance

Childcare vouchers

Job summary

ICON Clinical Research is seeking a Clinical Trial Manager to oversee day-to-day trial operations, supporting teams and stakeholders to deliver high-quality outcomes across our clinical programmes.

You will plan and manage all aspects of trials, collaborate with cross-functional teams to implement protocols, build strong investigator relationships, ensure regulatory compliance, and address design, vendors, and risk management.

Qualifications

• University degree in medicine, science, or equivalent combination of education & experience.
• Demonstrated ability to drive the clinical deliverables of a study.
• Subject matter expertise in the designated therapeutic area.
• Prior monitoring experience is highly preferred.
• Previous experience as a Clinical Trial Manager.

Responsibilities

• Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.
• Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
• Build and manage strong relationships with trial investigators and stakeholders.
• Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.
• Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.

Skills

Clinical trial management

Stakeholder management

Regulatory compliance

Study deliverables

Education

University degree in medicine, science, or equivalent combination of education & experience

Job description

ICON Clinical Research is seeking a Clinical Trial Manager to oversee day-to-day trial operations, supporting teams and stakeholders to deliver high-quality outcomes across our clinical programmes.

You will plan and manage all aspects of trials, collaborate with cross-functional teams to implement protocols, build strong investigator relationships, ensure regulatory compliance, and address design, vendors, and risk management.