Remote & On-Site Clinical Research Associate - Site Management

Scorpion Therapeutics; New Jersey; Hybrid; USD 65,000 - 90,000; Full time

Job summary

Novo Nordisk is seeking a Clinical Trial Site Coordinator in New Jersey to oversee site engagement, trial start-up, patient recruitment, retention, and data management to ensure timely delivery of studies.

The role requires strong communication with IRBs, vendors, and cross-functional teams, along with a focus on regulatory compliance, data quality, and on-time trial milestones. Some travel may be required in a hybrid work setup.

Qualifications

• Bachelor's degree in a science-related field or RN.
• Minimum 3 years of GCP clinical trial experience.
• At least 2 years in site management and logistics.
• Knowledge of ICH-GCP, medical terminology, and clinical systems; excellent communication and stakeholder management skills.

Responsibilities

• Serve as primary site contact and liaison for study teams.
• Support site activation through regulatory submissions and training.
• Manage trial systems and data quality at the site.
• Track recruitment, enrollment, and data integrity.
• Assist with trial closure and audits; participate in cross-functional reviews.

Skills

GCP knowledge

Site management

Stakeholder management

Communication

Education

Bachelor's degree in science-related field

RN

Tools

Clinical trial systems

Job description

Novo Nordisk is seeking a Clinical Trial Site Coordinator in New Jersey to oversee site engagement, trial start-up, patient recruitment, retention, and data management to ensure timely delivery of studies.

The role requires strong communication with IRBs, vendors, and cross-functional teams, along with a focus on regulatory compliance, data quality, and on-time trial milestones. Some travel may be required in a hybrid work setup.