Senior, Clinical Trial Manager, CTM - FSP (North America, EAST COAST)

Thermo Fisher Scientific; North Carolina; Remote; USD 90,000 - 130,000; Full time

Job summary

A leading company in the Pharmaceutical/Biotech industry is seeking a Senior Clinical Trial Manager. This role is crucial in coordinating activities across clinical trials, ensuring adherence to regulatory standards, and managing relationships with CRO partners. The position will leverage your expertise in oncology/neuroscience, offering the opportunity to impact clinical study success while working remotely from the East Coast.

Qualifications

• At least 3 years of independent CRA experience in pharma or CRO setting.
• Experience as Lead CRA managing multi-site international studies.
• Strong knowledge of GCP, ICH, and clinical documentation.

Responsibilities

• Coordinate clinical activities, oversee CRO and site management.
• Manage CRO relationships and support study start-up.
• Conduct co-monitoring visits and prepare for audits.

Skills

Organization

Communication

Teamwork

Proficiency in clinical trial software

Education

Life sciences or medical degree

CRA certification

Job description

Senior, Clinical Trial Manager, CTM - FSP (North America, EAST COAST)

Join to apply for the Senior, Clinical Trial Manager, CTM - FSP (North America, EAST COAST) role at Thermo Fisher Scientific.

This role involves coordinating clinical monitoring activities, overseeing CRO site management, and co-monitoring international Phase 3 studies in compliance with GCP, SOPs, and regulatory standards. The position requires collaboration within a matrix organization, building investigator relationships, and ensuring timely, quality study delivery.

Work Schedule: Standard (Mon-Fri)

Location: US, Remote (East Coast preferred; CST considered)

Main Responsibilities

• Coordinate clinical activities, oversee CRO and site management, support study start-up, feasibility review, and site selection.
• Ensure documentation and system tasks are completed timely; support CRO training and monitor study progress.
• Manage CRO relationships, participate in bid processes, and support medical liaison activities.
• Conduct co-monitoring visits, review data, ensure documentation quality, and prepare for audits.
• Contribute to SOP updates, training, and continuous improvement initiatives.

Qualifications & Experience

• Life sciences or medical degree; CRA certification preferred.
• At least 3 years of independent CRA experience in pharma or CRO setting, with oncology or neuroscience focus.
• Experience as Lead CRA, managing multi-site international studies.
• Strong knowledge of GCP, ICH, and clinical documentation.
• Ability to travel 20-25%.

Skills

• Proficiency in clinical trial software, organization, communication, and teamwork skills.

Employment Details

• Full-time, Research & Science sector, Pharmaceutical/Biotech industry.