Remote Clinical Research Associate II - West US

Parexel; Salem (OR); Remote; USD 70,000 - 110,000; Full time

Job summary

Parexel is seeking a Clinical Research Associate to act as the primary site contact and site manager across all phases of a clinical study. You will build strong site relationships, monitor data integrity, ensure patient safety, and coordinate with sponsor teams.

The role involves remote and on-site activities and requires knowledge of ICH-GCP and regulatory standards. The ideal candidate has 2+ years of direct site monitoring experience, a science-related bachelor’s degree, and excellent

Qualifications

• Minimum 2 years of direct site monitoring experience in bio/pharma/CRO.
• Bachelor’s degree preferred in science and/or biology.
• Fluent in English with strong written and verbal communication.

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-GCP, Sponsor SOPs, Local laws and regulations, protocol, and Site Monitoring Plan.
• Gains an in-depth understanding of the protocol and related procedures.
• Coordinates and manages tasks in collaboration with sponsor roles to achieve Site Ready.
• Participates in site selection and validation activities.
• Performs remote and on-site monitoring and oversight with various tools to ensure data integrity and patient safety.
• Documents visit reports and regulatory documentation timely and accurately.
• Communicates with Investigators and site staff on protocol conduct, recruitment, and regulatory documentation.
• Identifies and resolves site performance, quality, or compliance issues and escalates as needed.
• Manages information in CTMS/eTMF and other systems per timelines.
• Contributes to CRA knowledge as a mentor and supports audits/inspections.

Education

Bachelor’s degree

Job description

Parexel is seeking a Clinical Research Associate to act as the primary site contact and site manager across all phases of a clinical study. You will build strong site relationships, monitor data integrity, ensure patient safety, and coordinate with sponsor teams.

The role involves remote and on-site activities and requires knowledge of ICH-GCP and regulatory standards. The ideal candidate has 2+ years of direct site monitoring experience, a science-related bachelor’s degree, and excellent