Remote CRA II: Site Management & Monitoring Lead

Parexel; Lansing (MI); À distance; USD 65 000 - 95 000; Plein temps

Résumé du poste

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’ll develop site relationships, ensure compliance with ICH-GCP, and conduct both remote and on-site monitoring to protect patient safety and data integrity.

The role requires a Bachelor’s degree in science/biology and at least 2 years of direct site monitoring experience in bio/pharma/CRO, with strong communication and problem-solving skills.

Qualifications

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

Responsabilités

• Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.
• Performs site management/monitoring activities in compliance with ICH-GCP and sponsor SOPs.
• 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 and oversight activities.

Connaissances

Fluent English and local languages

Excellent communication skills

Clinical research knowledge

GCP/ICH knowledge

Site management experience

Monitoring and QA

MS Office and clinical IT tools

Data analysis

Independent judgement

Cross-cultural collaboration

Formation

Bachelor’s degree in science/biology

Outils

Clinical Trial Management System

Description du poste

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’ll develop site relationships, ensure compliance with ICH-GCP, and conduct both remote and on-site monitoring to protect patient safety and data integrity.

The role requires a Bachelor’s degree in science/biology and at least 2 years of direct site monitoring experience in bio/pharma/CRO, with strong communication and problem-solving skills.