LIMS Administrator
7 days ago
This Application Administrator configures software applications to meet laboratory requirements. Your logical thinking and eye for detail will be essential in programming solutions to a variety of challenges. You will fill a critical role by ensuring clinical goals are achieved through a complete and accurate system.
Responsibilities- Provide timely and accurate support for laboratory information management systems and other supported applications for internal and external users;
- Develop system enhancements and document processes where appropriate;
- Attend to requested updates and tickets – resolution will include clarifying requirements, coding, testing, and deploying updates;
- Update and maintain system documentation (Technical Manual, Design Specification, etc.);
- Create workaround procedures when standard procedures have failed and ensure issues are resolved in a timely fashion;
- Investigate unexpected events and escalate urgent problems requiring more in-depth knowledge to appropriate internal resources; and
- Perform deployments of application/product releases to production environments globally.
- responsible for updating, maintaining, and troubleshooting a commercial LIMS.
- After extensive customization, a complex set of features overlays the purchased system.
- Understanding both the native functionality and the added logic is required to ensure that configuration is reliable and efficient.
- Engineers use that knowledge to add new laboratory tests, enter study-specific programming, and coordinate the interface of new instruments to the system. T
- Review the work of peers and act as first-line support for laboratory technologists.
- Bachelor's Degree in Information Systems, Mathematics, or related field;
- Good organizational skills, very detail oriented;
- Strong analytical and communication skills;
- Basic programming knowledge;
- Experience working with SCC Soft Computer systems is a plus; and
- Previous experience working in a commercial LIMS such as LabVantage is a plus.
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Why Medpace?People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Awards
Named a Top Workplace in 2024 by The Cincinnati Enquirer
- Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
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