Remote Clinical Research Associate / Senior CRA

Parexel; Hartford (CT); On-site; USD 70,000 - 110,000; Full time

Job summary

Parexel FSP is seeking a Clinical Research Associate (CRA/Sr CRA) in the United States to oversee monitoring at assigned sites and collaborate with local study teams. The role emphasizes adherence to ICH-GCP, data integrity, and site management across multiple sites.

Responsibilities include site qualification, initiation, monitoring, data verification, and ensuring timely study conduct in accordance with sponsor standards. Some travel may be required to ensure study milestones are met.

Qualifications

• Excellent knowledge of ICH-GCP and GMP/GDP basics.
• Experience with clinical trial monitoring and CTMS is desirable.
• Ability to travel nationally/internationally as required.

Responsibilities

• Oversee site qualification visits and regulatory submissions as needed.
• Conduct monitoring visits (remote and onsite) and data verification per Monitoring Plan.
• Train and support site staff on study-related matters and document training.
• Ensure timely reporting of site activities and query resolutions.

Skills

Attention to detail

Communication skills

Collaboration

Negotiation

English proficiency

Local language fluency

Education

Bachelor’s degree in life science or related

Job description

Parexel FSP is seeking a Clinical Research Associate (CRA/Sr CRA) in the United States to oversee monitoring at assigned sites and collaborate with local study teams. The role emphasizes adherence to ICH-GCP, data integrity, and site management across multiple sites.

Responsibilities include site qualification, initiation, monitoring, data verification, and ensuring timely study conduct in accordance with sponsor standards. Some travel may be required to ensure study milestones are met.