Remote CRA II: Site Monitoring & Trial Oversight

Parexel; Dover (DE); Remote; USD 70,000 - 100,000; Full time

Job summary

Parexel is seeking a Clinical Research Associate to act as the primary site contact and manage allocated sites across trial phases. You will monitor site performance, ensure regulatory compliance, and support initiation through close-out visits.

This role requires working with data, regulatory documents, and cross-functional teams to maintain trial integrity and subject safety in a fast-paced environment.

Qualifications

• Minimum 2 years of direct site monitoring experience in bio/pharma/CRO.
• Bachelor’s degree preferred with a strong emphasis in science and /or biology.

Responsibilities

• Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.
• Performs clinical study site management/monitoring activities in compliance with ICH-GCPs, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan.
• Gains an in-depth understanding of the study protocol and related procedures.
• Coordinates and manages tasks with sponsor roles to achieve Site Ready.
• Performs remote and on-site monitoring & oversight activities to ensure data quality and patient safety.

Skills

Fluent English

Site management

Monitoring visits

ICH-GCP knowledge

Data/documentation skills

MS Office / clinical IT apps

Education

Bachelor's degree

Tools

CTMS

eTMF

EDC systems

Job description

Parexel is seeking a Clinical Research Associate to act as the primary site contact and manage allocated sites across trial phases. You will monitor site performance, ensure regulatory compliance, and support initiation through close-out visits.

This role requires working with data, regulatory documents, and cross-functional teams to maintain trial integrity and subject safety in a fast-paced environment.