Clinical Documentation Specialist

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

At the forefront of the staffing industry, Artech is a minority and women-owned business enterprise (MWBE) committed to maximizing global workforce solutions on behalf of its clients. Artech's deep heritage, proven expertise and insightful market intelligence has secured long-term partnerships with Fortune 500 and government clients seeking world-class professional resources.

Job Description

Title: Clinical Documentation Specialist - C
Location: North Chicago, IL
Duration: 4 Months
Job ID: 005829

Qualifications

Job Description: This position is Non Exempt. Hours over 40 will be paid at Time and a Half.

• Manage Phase I – IV study activities, including: participate in the development of protocols, participate in CRF design, manage drug supply, initiate and monitor sites directly or indirectly, monitor CRO activities and provide training as necessary, act as primary liaison between central IRB and sites, assist in the management of central lab, CRO and sites, assist with identification and recruitment of study sites, review and track contracts, review regulatory documents prior to drug shipment, participate and present at Investigator Meetings and other training sessions.
• 5+ Years Experience Level.

Qualifications Details

Required Skills:

• Must have experience working in a lab environment such that the experience can be applied to the current position.
• The candidate must have proven experience with good technical writing skills and attention to detail.
• The position involves completing multiple documentation-related activities including: writing method validation protocols and reports, verification of laboratory records, preparation of data summaries, and entering information into databases.
• Must have experience with Microsoft Word, Excel, ChemDraw, and databases.
• Start date is asap.

Additional Information

All your information will be kept confidential according to EEO guidelines. If you believe you're qualified for this position and are currently in the job market or interested in making a change, please give me a call as soon as possible at [phone]