Search TSR Jobs

About TSR:

TSR is a relationship-based, customer-focused IT and technical services staffing company.

For over 40 years TSR, Inc. and its wholly owned subsidiary, TSR Consulting Services, have prospered in the Information Technology staffing business, earning the respect of companies both large and small with well refined candidate screening, timely placement, and a real understanding of the right skill sets required by our clients.

Mission & Vision

We do not believe in building a vision around the company but building a company around our vision, which is simply;

Every employee’s voice matters, their effort is appreciated, and their talent is rewarded.

We challenge each employee daily, to raise the bar on how we treat our consultants and candidates. For far too long in this industry, candidates have been ghosted, lied to, or placed at a client and then forgotten about. Each day our staff works tirelessly at qualifying and placing, top talent with our clients, in a compassionate and caring manner.

Not every candidate is a match for the job, but every candidate and consultant will be treated with respect and professionalism.

Documentation (QC) Specialist

Job Description

  • Location: New Brunswick, NJ
  • Type: Contract
  • Job #75044

Our client, a leading pharmaceutical company, is hiring a Documentation (QC) Specialist consultant on a contract basis.

Work Location
New Brunswick, NJ/Hybrid

Summary

Documentation Management Specialist
This is a Hybrid 50/50 Role
New Brunswick, NJ
Work Schedule: Mon – Fri, Business Hours

clientDocs is an initiative to enhance the enterprise management of controlled documents by moving from several document management systems into a unified solution within Veeva Vault.

Support following activities related to clientDocs project:
• New System protoype testing
• User Acceptance testing
• Migration mapping from current system to clientDocs
• Migration verification activities
• Assist with training activities
• Draft new procedures, update existing procedures
• Integration of hCelgene specifications
• Document management experience in a systems related environment.
• Experience with IT related project activities (Migration verification, User Acceptance testing)
• Change management experience.
• Ability to set priorities and deliver results independently.
• Organization awareness and ability to work well cross-functionally with IT, etc.
• Detail-oriented with a quality mindset.
• Strong verbal and written communication skills.
• MS Office experience.
• Excellent meeting facilitation and project management skills.

Support following activities related to clientDocs project:
• New System protoype testing
• User Acceptance testing
• Migration mapping from current system to clientDocs
• Migration verification activities
• Assist with training activities
• Draft new procedures, update existing procedures
• Integration of hCelgene specifications

Education and Experience Required:
• Minimum of a Bachelors degree.
• Minimum 4 years experience in the pharmaceutical industry or related field.
• Document management experience in a systems related environment.
• Experience with IT related project activities (Migration verification, User Acceptance testing)
• Change management experience.
• Ability to set priorities and deliver results independently.
• Organization awareness and ability to work well cross-functionally with IT, etc.
• Detail-oriented with a quality mindset.
• Strong verbal and written communication skills.
• MS Office experience.
• Excellent meeting facilitation and project management skills.

 

Include a message to the recruiters.
Attach a resume file. Accepted file types are DOC, DOCX, PDF, HTML, and TXT.
Review our Privacy Policy for more information.

We are uploading your application. It may take a few moments to read your resume. Please wait!