AL
Editor III
Artech LLC
- 🇺🇸 United States
- Hybrid
- 12 hours ago
- $45.00 – $48.41 / hour
12 hours ago
Job location: Mettawa, IL (3 days onsite and 2 days remote)
Job duration: 24+ months
Standard Business hours
2-3 rounds of interviews
Top 3-5 skills:
1. Highly detail oriented, and great communication skills, able to work independently as needed
2. Experienced medical editing
3. Fact checking of medical materials
4. Proactive about seeking out work when presented with downtime
5. Ability to pivot or shift gears quickly, working in a high volume, fast-paced environment
Job Description:
Responsibilities: Manages review and approval process for promotional, non-promotional and internal use materials. Manages electronic approval system, user access, user training and workflows. Supports FDA Ad Promo Submissions. Supports QC and regulatory reviews of the materials.
- Coordinate promotional and non-promotional materials review and approval processes
- Maintain in-depth knowledge of approval process routing grids per SOP and route the materials for approvals accordingly
- Attend the PRC meeting discussions to answer any editorial questions/concerns
- Collaborate with marketing operations on prioritization for routine approvals as well as during major campaign launches and label updates.
- Complete editorial review of promotional and non-promotional materials, final reviews, reapprovals and other review types as necessary
- Archive OPDP correspondence per guidance from Reg Ad promo lead
- Contribute to development and update of departmental work instructions
- Prepare materials, form 2253, cover letter and send them over to Reg Operations for publishing and OPDP submission
- Support other departmental initiatives as needed (e.g. process improvements)
- Bachelors degree in technical or science related discipline or related work experience
- Preferred: 3 years in regulatory, quality or related area
Editor III · Artech LLC