Clinical Research Assistant — Growth & Benefits

Pinnacle Clinical Research; Dallas (TX); On-site; USD 42,000 - 66,000; Full time

Benefits offered by this job

401k

Insurance package

PTO 3 weeks

14 holidays

Scrub voucher

Job summary

Summit Clinical Research Solutions in Dallas is seeking a diligent Clinical Research Assistant to support coordination of trials and regulatory activities. You will assist with study documents, regulatory submissions, and monitor preparation, while maintaining confidentiality and compliance with FDA/ICH GCP/HIPAA norms.

The role involves coordinating multiple projects, interacting with investigators, sponsors, and site staff, and leveraging CTMS to track progress and data accuracy.

Qualifications

• Ability to demonstrate competence in oral and written communication.
• Must be organized, attentive to detail, and professional.
• Flexibility with changing priorities and diplomatic communication.
• Medical terminology knowledge.
• Proficient with common office software and eCRF systems.

Responsibilities

• Assist with creation and completion of study documents and study prep.
• Support regulatory submissions and maintain regulatory files.
• Liaise with sponsors as needed.
• Prepare for study monitor visits and create reports.
• Conduct patient assessments, coordinate visits, and collect essential data.
• Screen and recruit subjects as directed and update CTMS.
• Coordinate multiple trials and communicate with team members.

Skills

Oral communication

Written communication

Organized

Attention to detail

Medical terminology

Education

GED or equivalent

2–4 years related experience

Tools

Microsoft Word

Microsoft Excel

Internet Explorer

Google Chrome

Mozilla Firefox

ECF/eCRF systems

Job description

Summit Clinical Research Solutions in Dallas is seeking a diligent Clinical Research Assistant to support coordination of trials and regulatory activities. You will assist with study documents, regulatory submissions, and monitor preparation, while maintaining confidentiality and compliance with FDA/ICH GCP/HIPAA norms.

The role involves coordinating multiple projects, interacting with investigators, sponsors, and site staff, and leveraging CTMS to track progress and data accuracy.