Neurology CRA I: Site Trials

AbbVie; Jersey City (NJ); Hybrid; USD 85,000 - 125,000; Full time

Job summary

AbbVie seeks a skilled professional to advance our clinical research programs by optimizing site engagement and trial execution. You will partner with investigators and site staff to uphold data integrity, protocol adherence, and high study performance across multiple sites.

Responsibilities include site evaluation, training, and ongoing monitoring under GCP guidelines, with emphasis on recruitment strategies and issue resolution. Strong collaboration and communication are essential.

Qualifications

• Experience leading clinical trial activities across sites and coordinating with investigators.
• Understanding of ICH-GCP guidelines, regulatory requirements, and data integrity principles.
• Ability to communicate effectively with diverse stakeholders and manage site relationships.

Responsibilities

• Serve as primary contact for investigative sites and provide trial information.
• Train and motivate site staff on trial protocols and patient treatment principles.
• Perform site evaluations, training, and monitoring in line with SOPs and regulations.
• Develop site engagement strategies and use CRM tools to track progress.

Skills

Clinical trial coordination

GCP knowledge

Site management

Cross-functional collaboration

Education

Bachelor’s degree in Life Sciences

Tools

CRM systems

Job description

AbbVie seeks a skilled professional to advance our clinical research programs by optimizing site engagement and trial execution. You will partner with investigators and site staff to uphold data integrity, protocol adherence, and high study performance across multiple sites.

Responsibilities include site evaluation, training, and ongoing monitoring under GCP guidelines, with emphasis on recruitment strategies and issue resolution. Strong collaboration and communication are essential.