Senior Phase I CRA - Remote

Fortrea; Minnesota; Remote; USD 100,000 - 135,000; Full time

Job summary

Fortrea is seeking a Senior Clinical Research Associate with a strong Phase I background to join our Phase I team in the United States. You will monitor study sites, manage data integrity, and oversee SAE reporting while coordinating with cross-functional teams.

The ideal candidate has 3+ years of clinical monitoring experience, Phase I exposure, and is able to travel 40-50% overnight. This role offers remote-friendly arrangements and ongoing opportunities within Fortrea's trials infrastructure.

Qualifications

• 3+ years of clinical monitoring experience.
• Phase I experience.
• 40-50% overnight travel.

Responsibilities

• Monitor clinical sites, conduct pre-study and initiation visits, maintain study files, liaise with vendors.
• Manage sites per project plans.
• Perform general on-site monitoring.
• Provide materials and training to staff for patient enrollment.
• Ensure informed consent and protocol adherence.
• Ensure data integrity of CRFs and data review.
• Oversee registry management and feasibility work.
• Complete SAE reporting and follow-up.
• CRF review and query resolution per guidelines.
• Assist training of new staff, including co-monitoring.
• Coordinate clinical projects as Local Project Coordinator.
• Perform other duties as assigned.

Skills

Clinical monitoring

Phase I experience

Travel willingness

Education

University degree or allied health certification

Job description

Fortrea is seeking a Senior Clinical Research Associate with a strong Phase I background to join our Phase I team in the United States. You will monitor study sites, manage data integrity, and oversee SAE reporting while coordinating with cross-functional teams.

The ideal candidate has 3+ years of clinical monitoring experience, Phase I exposure, and is able to travel 40-50% overnight. This role offers remote-friendly arrangements and ongoing opportunities within Fortrea's trials infrastructure.