This position will work with the central scheduling manager with retrospective and active data entry to support Non-clinical studies within an electronic database.
Additionally, this position will support scheduling in-vivo activities as needed to ensure a timely proposed schedule for non-clinical study directors using project management software.
The contract research associate will assist with randomization, protocol definition, data entry, animal identification updates, and schedule adjustments to streamline scheduling efficiencies.
Primary Responsibilities Include :
- Collaborate with central schedule manager to maintain centralized schedule for in-vivo, ex-vivo, and downstream analysis
- Retroactive data collection in electronic data base
- Assist in protocol definition using electronic software
- Updating schedule in real time using project management software
- Communicating with study directors, study coordinators, and vivarium personnel to ensure alignment on schedule updates
- Perform other duties as assigned
Desired Education and Skills :
- Bachelor’s Degree preferred, equivalent combination of education, training and experience may be substituted for degree
- Knowledge of GLP regulations and guidelines
- 1-3 years’ experience using project management systems such as Workfront, Provantis, Power BI or Microsoft Project
- Strong organizational skills
- Ability to multi-task and manage multiple projects
- Strong interpersonal and communication skills
- Ability to work independently and manage time appropriately based on priorities
LI-Onsite
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The contract research associate will assist with randomization, protocol definition, data entry, animal identification updates, and schedule adjustments to streamline scheduling efficiencies. This position will work with the central scheduling manager with retrospective and active data entry to supp...
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