REMOTE::Global Regulatory Affairs Project Coordinator/Manager Needed

timePosted 2 days ago location United States salarySalary undisclosed
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Job Description


Hope You are Doing Good,

I am hiring a Consultant for one of my client's requirements. Job Description for the same is written below. If you find yourself comfortable with the requirement please reply back with your updated resume

Position:- Global Regulatory Affairs Project Coordinator/Manager II

Location:- Jersey City/NJ (REMOTE)

Duration:- 06 Months Contract

and GC

Job Description

Drive Global Regulatory Affairs innovation efforts

o Actively engage and collaborate with the Innovation Lead and other GRA leaders to achieve the goals set out in the innovation agenda

  • Employ solutions to enhance processes, technology and activities

o Lead cross-organizational innovation initiatives and ensure that team members are aware of and meet all expected deliverables and outcomes.

o Develop and manage timelines and milestones for innovations

o Raise new ideas and facilitate meetings to brainstorm and create new initiatives

o Drive review of analogues and precedents to proactively avail the GRA team with cutting edge technologies and potential and relevant innovation opportunities

o Identify and explore vendors and off the shelf technologies to supplant existing manual processes or current technology

  • Responsible for coordinating and facilitating cross functional meetings

o Managing initiative and project team meetings

o Develop agendas, track actions and communicate meeting outcomes.

o Ensure plans are implemented in accordance with timelines and any issues, challenges or deviations are escalated for resolution in a timely manner.

  • Prepare regulatory portfolio and management presentations for meetings and forums

  • Provide project management support for various GRA functions such as the Labeling and Document Management groups.

  • Interface with senior management on various projects and initiatives

  • Support efforts to develop and maintain key performance indicators


  • Required: 2-5 years project management support experience.


o Knowledge of the drug development process and/or Regulatory Affairs.

o Demonstrated contributions that have helped innovatively transform processes, technology, roles, organizational activities and collaborations

o The candidate should have exceptional oral and written communication skills and be knowledgeable with software applications that will be regularly used (in particular; Excel, MS Project Server, SharePoint and PowerPoint).

o Certification in project management (PMP, CAPM) is desired but not required.

  • Minimum: Bachelors (Biological sciences preferred)
- provided by Dice