Remote CRA II — Clinical Trial Site Lead (West US)

Parexel; Santa Fe (NM); Remote; USD 65,000 - 110,000; Full time

Job summary

Parexel is seeking a Clinical Research Associate to serve as the primary site contact and site manager across all study phases. You will build strong site relationships, monitor data quality, ensure patient safety, and coordinate with sponsor teams to achieve Site Ready.

The role involves on-site and remote monitoring, regulatory documentation, and collaboration with Investigators. The ideal candidate has at least 2 years of direct site monitoring experience in bio/pharma/CRO, with a Bachelor’s

Qualifications

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

Responsibilities

• Develops strong site relationships and ensures continuity through all trial phases.
• Performs site monitoring in accordance with ICH-GCP, sponsor SOPs, local laws, protocols and Site Monitoring Plan.
• Gains understanding of the study protocol and related procedures.
• Coordinates and collaborates with sponsor roles to achieve Site Ready.
• Participates in site selection and validation activities.
• Performs remote and on-site monitoring to ensure data accuracy and patient safety.
• Maintains Trial Master File and CTMS documentation.

Skills

Site relationship management

Clinical trial monitoring

ICH-GCP & regulatory compliance

Data quality & integrity

Communication skills

Independent judgment

MS Office / clinical IT apps

Multi-protocol/site management

Time management

Problem solving

Education

Bachelor’s degree in science/biology

Job description

Parexel is seeking a Clinical Research Associate to serve as the primary site contact and site manager across all study phases. You will build strong site relationships, monitor data quality, ensure patient safety, and coordinate with sponsor teams to achieve Site Ready.

The role involves on-site and remote monitoring, regulatory documentation, and collaboration with Investigators. The ideal candidate has at least 2 years of direct site monitoring experience in bio/pharma/CRO, with a Bachelor’s