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Company | Precision Medicine Group |
Address | Houston, TX, United States |
Employment type | FULL_TIME |
Salary | |
Category | Technology, Information and Internet |
Expires | 2023-08-13 |
Posted at | 10 months ago |
Position Summary:
- Monitoring clinical site inventories and replenishing/refreshing supplies as necessary, but within constraints of the contract
- Receiving, inspecting, and logging in patient specimens
- Coordinating sample shipment/receipt with clinical sites and package carriers
- Receiving laboratory supplies
- May require to process a simple task in the lab to assist PBMCs processing, or cell culture maintenance
- Kit component inventories and ensuring that components are used in a first in/first out (FIFO) manner
- Coordinating clinical site management with input from other PFM team members
- Providing training to clinical sites as requested
- Demonstrating the ability to multi-task on a daily basis, prioritize project goals, pay strict attention to detail, and meet customer demands
- Picking up samples locally (on occasion): Must own a vehicle and have a valid driver's license as the position involves sample pickup as needed, as a backup to the other staff, at local sites.
- Ensuring timely kit assembly and distribution
- Input kit and sample inventories in BSI database and suggesting improvements
- Communicating with package couriers and customers
- Tracking kits for expiration, delivery status, etc.
- Contributing to portions of the laboratory project work scopes as needed
- Sending out sample prenotification and receiving (sample and reagents) notifications to scientific team
- Maintaining an organized and safe lab environment by helping to enforce GCP/CLIA compliance.
- Bachelor's Degree or equivalent in Science, Business or related field
- Ability to lift and carry between 25-150 lbs.; frequently required to sit, grasp, and use right/left finger dexterity
- Experience with BSI or equivalent database
- Position requires occasional long hours, work on the evenings, weekends, and holidays
- Must be able to read, write, speak fluently and comprehend the English language
- Someone who is a good team player, meticulously detailed and organized, can work under pressure and has good oral and written communication skills
- Have a documentation background in a laboratory setting with respect to regulatory guidelines (cGMP, cGLP or ISO) and SOPs
- Proficient computer skills with mid to advanced level in MS Office products (Word, Excel, PowerPoint, Outlook) and Adobe
- Good organizational and people skills
- Familiar with LIMS or BSI system
- Understanding of current GLP or CAP/CLIA/ISO standards
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