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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.

Clinical Labeling Specialist

Job Description

  • Location: New Brunswick, New Jersey
  • Type: Contract
  • Job #77904

Our client, a leading pharmaceutical company, is hiring a Clinical Labeling Specialist on a contract basis.

Work Location:
New Brunswick, NJ – 100% on-site

Onsite full-time during training period with option to work 50% from home after completion of training.

Knowledge/Skills Required/Education:

  • Bachelors degree or equivalent in pharmacy, engineering, business or life sciences required
  • Ability to plan, manage and execute multiple projects and to deliver against critical timelines in a fast-paced, rapidly changing environment.
  • Strong project management skills and detail oriented.
  • Possesses solid oral and written communication skills.
  • Excellent decision making and organizational skills.
  • Ability to effectively communicate ideas and to influence others to achieve results.
  • Ability to understand and apply regulatory and cGMP principles.
  • Thorough understanding of pharmaceutical or medical terminology.
  • Proficiency in standard MS office technology, including Microsoft Suite (Outlook, PowerPoint, Excel) and additional applications such as Adobe. Willing to learn additional applications as needed.
  • Experience working on multi-disciplinary teams and projects.
  • Good knowledge of rigorous pharmaceutical and/or scientific documentation practices and change control processes (e.g. revision control) is preferred


  • Supports timely delivery of clinical supplies through effective management of assigned projects.
  • Manages multiple projects and tracks all activities and milestones related to assigned projects. Identifies and reports issues to appropriate levels of management in a timely manner.
  • Generates label vendor specifications in accordance with relevant regulatory requirements for assigned projects.
  • Works with external partners to ensure clinical labels are created with exacting specification.
  • Generates clinical labeling source documentation as required.
  • Reviews and approves vendor generated label proofs/specifications and other related documents.
  • Utilizes electronic verification software to perform check on label proof. Routes final label for review and approval accordingly.
  • Participates in assigned training including cGMP and safety training
  • Ensures regulatory, cGMP, GDP compliance of activities in assigned areas of responsibility. Reports any deviations to the appropriate management.
  • Works cross-functionally with individuals and project teams in various areas.
  • Liaises with responsible Trial Supplies Manager on aspects of clinical supplies packaging and labelling design and study requirements and resolves issues.


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