Global Regulatory Intelligence & Policy (GRIP) Associate
: Job Details :


Global Regulatory Intelligence & Policy (GRIP) Associate

Redbock - an NES Fircroft company

Location: Basking Ridge,NJ, USA

Date: 2025-01-09T04:23:45Z

Job Description:

*Must be W2*

Location: 100% remote

Length: 12+ months

Duties/Responsibilities:

Under direction of GRIP leadership, provide following support to the global team:

Trackers:

  • Design, build, populate, organized, logical spreadsheets, with filtering capabilities and appropriate permissions that will be used to track various external events and company participation at these events
  • Health authority public meetings and conferences
  • Release of draft & final government documents
  • Team Responses to internal queries
  • Internal metrics
  • Trackers will be visible to all global reg affairs, R&D, and select other parts of business

Share Point & Teams:

  • Design and organize folder structures in team share point and Microsoft teams
  • Set permissions, upload documents, extract links for other communications
  • Above trackers will be housed here as well as other documents (analyses, position papers, reports, etc) that may also appear in above trackers via links

Newsletter & Briefings:

  • Assist with build of team newsletter/briefing and its distribution (via e-mail, Word, Power Point or other systems)
  • Communications - Provide communications support by contributing to the visual appeal and impact of deliverables (e.g. newsletter/briefing, trackers, share point, teams, slides)

Distribution:

  • Create and maintain standard distribution lists for team deliverables

Searching:

  • Support team with searches using a number of public and licensed search tools, and use this info to routinely populate select trackers

Tracking:

  • Tracking key deadlines, GRIP deliverables and meeting actions (truly tracking and not project managing)

Skills/Requirements:

  • Excellent organizational skills,
  • Good version control
  • Can standardize and document basic processes
  • Can easily shift between projects and priorities
  • Communication skills – with focus on visual and written
  • Attention to detail
  • Flexible & adaptable
  • Can work independently, but knows when to seek input
  • Excel experience: design, build, populate, organized, logical spreadsheets, with filtering capabilities that will be used to track various external events and internal metrics
  • Share Point & Teams experience: high level of working competency of key features, non-technical design and daily operation
  • Experience with Word, PowerPoint, Google and other internet search tools
  • Bachelor's degree
  • Some prior experience working in biopharma would be ideal, as it helps with some of the terminology, and understanding the organization, but not absolutely required if candidate is otherwise strong
  • Exposure to regulatory affairs preferred

Apply Now!

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