Senior CRA II – West US (Remote)

Parexel; Olympia (WA); 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 site manager across all trial phases. You will build strong site relationships, monitor conduct per ICH-GCP, and ensure data integrity and patient safety across multiple sites.

The role emphasizes understanding the protocol, coordinating with sponsor teams, and supporting audits. Remote work may be possible; a Bachelor’s degree in science is preferred.

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 site monitoring activities in accordance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents.
• Gains an in-depth understanding of the study protocol and related procedures.
• Coordinates and manages various tasks in collaboration with other sponsor roles to achieve Site Ready.
• Participates and provides inputs on site selection and validation activities.
• Performs remote and on-site monitoring & oversight activities using various tools to ensure data quality and patient safety.
• Communicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, regulatory documentation, site audits/inspections and overall site performance.
• Identifies, assesses, and resolves site performance, quality or compliance problems and escalates as appropriate.
• Manages and maintains information and documentation in CTMS and ETMF and other systems as appropriate.

Skills

Site management

GCP/ICH knowledge

Communication skills

Data analysis

MS Office

Independent judgement

Multi-protocol work

Remote/On-site monitoring

Education

Bachelor's degree preferred

Job description

Parexel is seeking a Clinical Research Associate to act as the primary site contact and site manager across all trial phases. You will build strong site relationships, monitor conduct per ICH-GCP, and ensure data integrity and patient safety across multiple sites.

The role emphasizes understanding the protocol, coordinating with sponsor teams, and supporting audits. Remote work may be possible; a Bachelor’s degree in science is preferred.