Clinical Documentation Specialist - Trials & Lab

Artech Information System LLC; Hanover Township (NJ); On-site; USD 70,000 - 90,000; Full time

Job summary

A staffing agency is seeking a Clinical Documentation Specialist located in North Chicago, IL. The role involves managing study activities for pharmaceutical trials, requiring over 5 years of lab experience, strong technical writing skills, and proficiency in Microsoft tools. The suitable candidate should be detail-oriented and prepared for a start date as soon as possible. This position is non-exempt with overtime paid at time and a half.

Qualifications

• 5+ years of experience level required.
• Experience working in a lab environment.
• Proven experience with technical writing and attention to detail.

Responsibilities

• Manage Phase I – IV study activities.
• Participate in the development of protocols.
• Act as primary liaison between central IRB and sites.

Skills

Lab environment experience

Technical writing skills

Attention to detail

Microsoft Word

Microsoft Excel

ChemDraw

Database management

Tools

ChemDraw

Databases

Microsoft Word

Microsoft Excel

Job description

A staffing agency is seeking a Clinical Documentation Specialist located in North Chicago, IL. The role involves managing study activities for pharmaceutical trials, requiring over 5 years of lab experience, strong technical writing skills, and proficiency in Microsoft tools. The suitable candidate should be detail-oriented and prepared for a start date as soon as possible. This position is non-exempt with overtime paid at time and a half.