Clinical Research Associate II — Site Monitoring & Oversight

Parexel

Boise (ID)

On-site

USD 70,000 - 100,000

Full time

7 days ago
Be an early applicant

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Job summary

Parexel is seeking a Clinical Research Associate to manage investigator sites, monitor trials from activation through close‑out, and ensure patient safety and data quality in line with GCP and sponsor standards.

The role requires at least 2 years of monitoring experience, English fluency, and the ability to travel 60–80%. A life sciences degree, driving license and passport are required.

Qualifications

  • Minimum 2 years relevant experience in clinical research site monitoring.
  • Fluent in English and in the native language of the country they will work in.
  • Ability to travel 60-80%.
  • Valid driver’s license and passport required.

Responsibilities

  • Ensure proper conduct of clinical trials in accordance with SMP, SOPs, GCP, and sponsor standards to achieve project goals, timelines and quality.
  • Manage assigned operational aspects for implementation of clinical trial activities at investigator sites from activation through database lock.
  • Serve as the primary point of contact for investigator sites and liaise with SCP to ensure quality of site delivery.
  • Interface with the study team, vendors, and investigator sites to facilitate information flow and issue resolution.
  • Conduct onsite and remote/electronic monitoring as required and ensure compliance with monitoring plans and regulatory requirements.

Skills

Clinical trial methodologies
ICH/GCP knowledge
FDA regulations knowledge
Monitoring experience
Travel ability
Fluent English
Driver's license
Passport

Education

Bachelor’s degree in life sciences

Job description

Parexel is seeking a Clinical Research Associate to manage investigator sites, monitor trials from activation through close‑out, and ensure patient safety and data quality in line with GCP and sponsor standards.

The role requires at least 2 years of monitoring experience, English fluency, and the ability to travel 60–80%. A life sciences degree, driving license and passport are required.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Senior Clinical Research Associate: Field Site Monitor
Senior Clinical Research Associate: Field Site Monitor

Parexel • Columbus (OH)

On-site
USD 65,000 - 90,000
Health insurance
Senior Clinical Research Associate — Field Monitoring Lead
Senior Clinical Research Associate — Field Monitoring Lead

Parexel • United States

Remote
USD 90,000 - 140,000
Senior Clinical Research Associate — Site Monitoring Lead
Senior Clinical Research Associate — Site Monitoring Lead

Parexel • Juneau (AK)

On-site
USD 85,000 - 120,000
Senior Clinical Research Associate - Site Monitoring
Senior Clinical Research Associate - Site Monitoring

Parexel • Cheyenne (WY)

On-site
USD 70,000 - 100,000
Remote Clinical Research Associate II – Site Monitoring
Remote Clinical Research Associate II – Site Monitoring

Parexel • Little Rock (AR)

On-site
USD 65,000 - 90,000
Senior CRA II — Field Site Monitor & Study Lead
Senior CRA II — Field Site Monitor & Study Lead

Parexel • Carson City (NV)

On-site
USD 70,000 - 100,000
Senior Clinical Research Associate II: Global Site Monitoring
Senior Clinical Research Associate II: Global Site Monitoring

Parexel • Honolulu (HI)

On-site
USD 70,000 - 90,000
Lead Clinical Trial Site Monitor
Lead Clinical Trial Site Monitor

Parexel • Ohio

Hybrid
USD 70,000 - 95,000
Senior Clinical Research Associate: Site Monitoring Lead
Senior Clinical Research Associate: Site Monitoring Lead

Parexel • United States

On-site
USD 100,000 - 140,000
Senior CRA: Site Leadership & Trial Monitoring
Senior CRA: Site Leadership & Trial Monitoring

Parexel • Montpelier (VT)

On-site
USD 70,000 - 100,000