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Document Training Coordinator
Bristol Myers Squibb
6 - 10 years
New Brunswick, NJ
Contract
Onsite
1 month ago
About the role
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 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 Director and Senior management staff
Assist with project coordination/project tracking as directed and as assigned by the 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
Skills
Pharmaceutical Manufacturing
Training
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