Lead Clinical Research Associate

SmartRecruiters, Inc.; Raritan (NJ); On-site; USD 51,000 - 73,000; Full time

Benefits offered by this job

12-month contract

Competitive pay

Job summary

Global Channel Management in New Jersey seeks an experienced Lead Clinical Research Associate to manage clinical sites, ensuring compliance with GCP, ICH, and regulatory requirements. The role focuses on cardiovascular trials and monitoring activities.

You will oversee field monitors, coordinate enrollment strategies, and work with CPL, CROs, and vendors to ensure trial integrity and on-time delivery.

Qualifications

• Minimum 5+ years site management with at least 2 years field monitoring.
• Knowledge of clinical trial standards and regulations (GCP/ICH/Regulations).
• Experience in cardiovascular therapeutic area.
• Proficiency with Medidata RAVE system.

Responsibilities

• Under supervision of Clinical Project Lead, oversees field monitors and site activities per Monitoring Plan.
• Implementation of enrollment and recruitment strategies.
• Assists in vendors’ selection processes.

Skills

Clinical monitoring

Regulatory knowledge

Vendor liaison

Enrollment strategies

Education

BS/BA, MS desirable

Tools

Medidata RAVE

Job description

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job.

Qualifications

Lead Clinical Research Associate needs:

• BS/BA, MS is desirable
• 5+ years of site management of which a minimum of 2 years field monitoring experience
• Knowledge of applicable standards and regulations for clinical trial
• Experience in Cardiovascular Therapeutic area
• Medidata RAVE system
• Under
  supervision of Clinical Project Lead, oversees performance of assigned
  field monitors and site activities in accordance with the Monitoring
  Plan, Protocol, Good Clinical Practice (GCP), ICH guidelines and federal
  regulations.
• The LCRA acts as a primary liaison between Field
  Based CRAs and the Clinical Project Lead (CPL). Additional
  responsibilities include:
• Implementation of enrollment and recruitment strategies
• Assistance in vendors’ selection processes

Additional Information

$45/hr

12 months