Senior Clinical Research Associate - Remote

Parexel; Juneau (AK); On-site; USD 90,000 - 130,000; Full time

Job summary

Parexel is seeking a Senior Clinical Research Associate to manage investigator sites, monitor trials, and oversee close-out activities in accordance with GCP and sponsor standards. The role requires engaging with site staff, ensuring patient safety, and maintaining site quality across multiple sites.

Key duties include driving enrollment, coordinating with the SCP, and handling protocol training and issue resolution while traveling 60-80% and holding a life sciences degree.

Qualifications

• Extensive knowledge of clinical trial methodologies, ICH/GCP and regulatory requirements.
• Minimum 2 years of monitoring experience at investigator sites.
• Fluency in English and in local language(s) where work will occur.

Responsibilities

• Manage site monitoring and close-out of investigator sites to ensure patient safety and study quality.
• Act as primary contact for investigator sites and coordinate with the Site Care Partner.
• Submit required reports, engage in site development and training, and oversee data query resolutions.

Skills

Clinical trial methodologies

ICH/GCP

FDA regulations

Site monitoring

English proficiency

Travel readiness

Driver’s license & passport

Education

Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent

Job description

Parexel is seeking a Senior Clinical Research Associate to manage investigator sites, monitor trials, and oversee close-out activities in accordance with GCP and sponsor standards. The role requires engaging with site staff, ensuring patient safety, and maintaining site quality across multiple sites.

Key duties include driving enrollment, coordinating with the SCP, and handling protocol training and issue resolution while traveling 60-80% and holding a life sciences degree.