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Training Coordinator - Lms - Pharma
Company | Clinovo |
Address | United States |
Employment type | CONTRACTOR |
Salary | |
Category | Medical Equipment Manufacturing,Biotechnology Research,Pharmaceutical Manufacturing |
Expires | 2023-08-11 |
Posted at | 10 months ago |
Recent experience in the Pharmaceutical industry is MUST.
Experience OR knowledge of clinical trials is MUST.
2Yrs. experience as a Training Coordinator is MUST
Title: Training Coordinator
Location: Fully Remote – anywhere is US
Duration: 12 + Months
Description:
The R&D Training Analyst/ Sr. Analyst is responsible for supporting the maintenance of R&D departmental documents and related training requirements. This role will liaise with R&D management to support the maintenance of training matrices and will also work closely with GxP Training in Quality Systems. The R&D Training Analyst/Sr. Analyst will provide training support for the GCDO Trial Specific Training initiative. The R&D Training Analyst/Sr Analyst may participate in inspection readiness activities and may support inspection and audit SMEs. The R&D Training Analyst/Sr. Analyst may assist in special projects as assigned by the R&D Process and Training department management.
Essential Functions
• Provide support for GCDO trial specific training initiative
• Assignment/Removal of training job roles to staff
• Monitor R&D P&T mailbox and respond to inquiries
• Tracking of training assignments and personnel
• Daily review of training reports
• Maintain list of R&D job roles by function
• Complete requests to create/maintain departmental training job roles
• Support the R&D organization review of departmental training job roles
• Maintenance of GXP training accounts
• Assist R&D Training management in creating and maintaining training matrices
• Participate in ongoing inspection readiness activities and provide support for inspections
• Performs other activities as directed by R&D Training management
• Knowledge of GxP regulations
• Familiarity with health authority regulations
• Knowledge of the conduct of clinical trials
• Experience with quality management activities
• Experience with Electronic Document Management Systems and Learning Management Systems experience
• Experience with developing and maintaining training matrices
• Proficiency in all Microsoft Office applications
• Organize, maintain and distribute cross-functional meeting minutes and agendas
• Ability to demonstrate values and strong organizational competencies
Required Knowledge, Skills, and Abilities
• 2+ years’ experience working in a pharmaceutical industry role preferred
• Ability to multi-task and shift priorities
• Exceptional organizational skills are a must
• Ability to communicate effectively, both verbally and in writing
• Good collaboration and networking skills
• LMS experience is very strongly preferred
Required/Preferred Education and Licenses
• BS or MS degree in Scientific or Clinical discipline preferred
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