In-House Clinical Research Associate

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

Role

Role: Clinical Trial Site Coordinator at Novo Nordisk, responsible for site engagement, trial start-up, patient recruitment, retention, and data management to ensure successful trial delivery.

Responsibilities

Responsibilities include acting as primary site contact, supporting site activation through regulatory and training processes, managing trial systems, tracking recruitment and data quality, and supporting trial closure and audits.

Engages cross-functionally with internal teams and external stakeholders like IRBs and vendors.

Requirements

Requirements: Bachelor's degree in a science-related field or RN, minimum 3 years of GCP clinical trial experience, with at least 2 years in site management and logistics.

Demonstrates knowledge of ICH-GCP, medical terminology, and clinical systems; excellent communication and stakeholder management skills.

Preferred

Preferred: experience with site activation, monitoring, and Novo Nordisk-specific protocols.

High-Value

High-Value: Focus on clinical trial site management within GCP-regulated environments, supporting Phase 1-3 trials, with some travel (0-10%). The role involves on-site and remote work, emphasizing collaboration across R&D, Clinical Operations, and external sites.