About this role

Company Description

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.

Job Description

  • This individual will be part of the Global Regulatory Affairs team and assists with planning, writing, compilation, and editing of periodic regulatory reports (i.e. DSURs, orphan annual updates, NDA annual reports, PBRERs).Β 
  • With oversight and guidance, contributes to the generation of product regulatory strategy documents (for products in phase 1-3 clinical development), labeling updates for marketed products, generation of FDA meeting requests and corresponding briefing materials, and other tasks as needed.Β 
  • Skills: Working knowledge of FDA and ICH requirements for standard regulatory documents and their maintenance.Β 
  • Excellent written and verbal communication skills, with ability to organize and manage multiple priorities. Proficiency in MS Word, Excel, and PowerPoint. Self-starter with the ability to work independently but seeking out guidance as needed. Technical aptitude to work across multiple information systems and databases with ability to troubleshoot. Sense of urgency and perseverance to achieve results. .Β 

Qualifications


  • Bachelor s degree and at least 5 years in Regulatory Affairs or relevant industry experience, or Master's, PharmD, PhD degree and 3 years in Regulatory Affairs or relevant industry experience

Additional Information


Β Sneha Shrivastava

Technical Recruiter (Clinical/Scientific)

Β Artech Information Systems LLC

360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960Β 

Office: 973.967.3348 | Fax: 973.998.2599

Connect with us on - LinkedIn | Facebook | Twitter

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Frequently Asked Questions

Is the salary disclosed for the Regulatory Affairs Specialist-V position at artechinformationsystemllc?
The salary for this Regulatory Affairs Specialist-V role at artechinformationsystemllc is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the Regulatory Affairs Specialist-V position at artechinformationsystemllc located?
This Regulatory Affairs Specialist-V role at artechinformationsystemllc is based in Bridgewater, Bridgewater, NJ, United States, NJ, us. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the Regulatory Affairs Specialist-V role at artechinformationsystemllc full-time or part-time?
This is listed as a Contract position. It is posted as a Regulatory Affairs Specialist-V role at artechinformationsystemllc.
How do I apply for the Regulatory Affairs Specialist-V position at artechinformationsystemllc?
Click the "Apply Now" button on this page. You will be redirected to artechinformationsystemllc's official application portal hosted on smartrecruiters where you can submit your application directly.
When was the Regulatory Affairs Specialist-V job at artechinformationsystemllc posted?
This Regulatory Affairs Specialist-V position at artechinformationsystemllc was posted on Mar 24, 2016. Apply as soon as possible β€” early applications are often reviewed first.
Regulatory Affairs Specialist-V
artechinformationsystemllc
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