DMPK Operations Coordinator
Inotiv · St Louis, MO · Yesterday
ManagementFull-time
About the role
Inotiv is seeking a DMPK Operations Coordinator to manage the daily workflow, tracking, and logistics for Drug Metabolism and Pharmacokinetics and non-clinical studies.
Responsibilities
- Assist with study scheduling, monitoring, and tracking to meet objectives, deliverables, and timelines
- Support Scientists/Operations with transferring critical information from client correspondences into relevant project management software structures
- Assist with development of relationships across departments/disciplines and with customers through frequent communication throughout the project to ensure clients’ needs are understood and addressed
- Communicate regularly with Scientific Leads and Program/Project Management from other Inotiv sites on multi-site projects
- Establish and communicate major milestones both internally and externally utilizing applicable software applications; discuss with team when escalation is required based on progress against deliverables/milestones
- Assist with regular meetings to review project activities and report status; communicate project challenges, scope changes, and timelines
- Maintain systems to analyze capacity for all resources (i.e., FTE/Equipment)
- Assist Management with maintaining departmental training records
- Provide assistance with departmental quote reviews
- Assist Scientific, Client Services, and Business Development team members with creation, delivery, and approval of change orders
- Assist in Sample Management activities including shipping, receiving, and logging samples/test articles upon receipt
- Coordinate departmental ordering and maintain inventory of routine supplies and chemicals
- Support Operations Management in all other aspects as needed
Requirements
- Bachelor’s degree with 2+ years of relevant experience
- Good organizational skills and detail-oriented
- Excellent communication and interpersonal skills with ability to work with personnel at all levels of the organization
- Ability to multi-task in a high-energy environment and manage multiple projects concurrently
- Ability to create and manage timelines
- Must be able to collaborate with functional departments and lead technical teams
- General understanding of GLP regulations
- Proficient in the use of computer software applications (e.g., Word, Outlook, Excel)
Working Conditions
- Work is normally performed in a typical interior office or laboratory environment
- Work may require use of PPE (Personal Protection Equipment)
Benefits
- Health and dental coverage
- Short- and long-term disability
- Paid time off
- Paid parental leave
- 401K participation with company match