Clinical Laboratory Research Scientist
Elanco
August 18, 2026
On-site
Fort Dodge, IA
Clinical Research and Development
Clinical Laboratory Research Scientist
Responsibilities:
- Work with Sponsors and Study Managers to define project requirements; develop and review protocols, validation methods, and sample analysis plans for clinical studies (GRP).
- Identify, develop, and implement new viral/bacterial culture methodologies, analytical methods, and laboratory technologies to improve clinical laboratory capabilities.
- Independently review, approve, and prepare raw data and laboratory data packages for statistical analysis, ensuring accuracy, completeness, and compliance with quality systems/standards (e.g., GxP, SOPs).
- Lead troubleshooting efforts, manage complex project workloads, and provide technical support to ensure timely study completion.
- Maintain laboratory infrastructure and ensure a clean, safe, organized environment; prepare and update SOPs and working procedures.
Minimum Qualifications:
- Bachelor’s Degree in Biology, Microbiology, Immunology, Animal Science, or related field (or equivalent experience).
- 5–8 years of hands-on laboratory experience.
- Demonstrated lab techniques (e.g., cell culture, assay design, molecular biology) and strong experimental design/data analysis knowledge.
Preferred Qualifications:
- Master’s or PhD in relevant scientific discipline.
- In-depth knowledge of clinical laboratory study design/execution and GxP-regulated workflows.
- Strong communication/collaboration; ability to present complex scientific data.
- Experience leading troubleshooting, managing complex projects, or mentoring junior scientists.
Additional Information:
- Travel: <10%
- Location: Fort Dodge, IA (on-site)
Benefits (as stated):
- Multiple relocation packages; two weeklong shutdowns (mid-summer and year-end) plus PTO; 8-week parental leave; 9 Employee Resource Groups; annual bonus offering; flexible work arrangements; up to 6% 401K matching.
Responsibilities:
- Work with Sponsors and Study Managers to define project requirements; develop and review protocols, validation methods, and sample analysis plans for clinical studies (GRP).
- Identify, develop, and implement new viral/bacterial culture methodologies, analytical methods, and laboratory technologies to improve clinical laboratory capabilities.
- Independently review, approve, and prepare raw data and laboratory data packages for statistical analysis, ensuring accuracy, completeness, and compliance with quality systems/standards (e.g., GxP, SOPs).
- Lead troubleshooting efforts, manage complex project workloads, and provide technical support to ensure timely study completion.
- Maintain laboratory infrastructure and ensure a clean, safe, organized environment; prepare and update SOPs and working procedures.
Minimum Qualifications:
- Bachelor’s Degree in Biology, Microbiology, Immunology, Animal Science, or related field (or equivalent experience).
- 5–8 years of hands-on laboratory experience.
- Demonstrated lab techniques (e.g., cell culture, assay design, molecular biology) and strong experimental design/data analysis knowledge.
Preferred Qualifications:
- Master’s or PhD in relevant scientific discipline.
- In-depth knowledge of clinical laboratory study design/execution and GxP-regulated workflows.
- Strong communication/collaboration; ability to present complex scientific data.
- Experience leading troubleshooting, managing complex projects, or mentoring junior scientists.
Additional Information:
- Travel: <10%
- Location: Fort Dodge, IA (on-site)
Benefits (as stated):
- Multiple relocation packages; two weeklong shutdowns (mid-summer and year-end) plus PTO; 8-week parental leave; 9 Employee Resource Groups; annual bonus offering; flexible work arrangements; up to 6% 401K matching.