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Quality - Document Training Coordinator
Quality - Document Training CoordinatorBristol Myers Squibb • New Brunswick, NJ, United States
Quality - Document Training Coordinator

Quality - Document Training Coordinator

Bristol Myers Squibb • New Brunswick, NJ, United States
2 days ago
Job type
  • Full-time
Job description

Job Title : Quality - Document Training Coordinator

Duration : 12 months

Location : New Brunswick, NJ (Hybrid)

50% onsite required

Pay range - $44 to 48.65 / hr on W2

Job Description : Work Schedule :

  • Normal business hours
  • Requirements : Project management experience, virtual / in-person training skills
  • Preferred : Bachelors degree (minimum Associates)
  • Reporting to the Director of IT Quality Assurance & Data Integrity, this contract position will perform project coordination, scheduling of training, and provide administrative support to the ITQA-DI projects.

Key responsibilities include :

  • Schedule and coordinate in-person or virtual training sessions
  • Plan and coordinate logistics with the sites and functions
  • Manage calendars and coordinate meetings, and training as planned by the ITQA-DI team
  • Inform site / function personnel about scheduled training, projects, and track their progress
  • Provide administrative support as required
  • Identify, escalate, and resolve issues which may negatively impact delivery of work.
  • Document and communicate status to the ITQA-DI Director and Senior management staff
  • Assist with project coordination / project tracking as directed and as assigned by the ITQA-DI Director and Senior Management Staff
  • Support project related work using SharePoint and Microsoft Teams, and MS Outlook.
  • Travel : Some domestic travel between client sites may be necessary.
  • Education : Minimum Associate degree required or Bachelors degree preferred
  • Basic Qualifications and Requirements :

  • Must have strong verbal and written communication skills, excellent organizational skills, and exceptional attention to detail.
  • Minimum of 2+ years of training coordination experience required in the Pharmaceutical Industry.
  • 2+ years experience with administrative duties, scheduling, and coordination of assigned tasks
  • Proficient in Microsoft Outlook, Teams, Excel, and PowerPoint
  • Preferred Qualifications
  • Good project management skills including experience in facilitating and implementing training related initiatives an
  • Proficient in Microsoft Project
  • Must have an excellent understanding of training and be proficient in handling various schedules.
  • Responsibilities :
  • Skills
  • Exceptional organizational skills including the ability to handle multiple assignments and prioritize work
  • Ability to work independently and effectively with a team.
  • Good interpersonal skills.
  • Good decision-making skills.
  • Ability to work collaboratively in a team setting
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    Quality Coordinator • New Brunswick, NJ, United States

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