Vivo Scientist II – CKD/CRM
Listed on 2026-10-13
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Research/Development
Research Scientist, Clinical Research
Our client is a global, research-driven pharmaceutical manufacturer focusing on treatment options for diseases and conditions for which there is no satisfactory treatment option to date. The company is looking for a In Vivo Research Scientist II to join the team. This is an amazing opportunity to work on cutting edge treatments and make a difference!
Pay rate: $40–$42/hour
Job type: 1 year contract
Location: Ridgefield, CT
Job SummarySeeking an In Vivo Research Scientist to conduct preclinical studies focused on chronic kidney disease (CKD) and cardio-renal-metabolic (CRM) models. The role requires hands-on rodent experience, independent study execution, data interpretation, troubleshooting, and compliance with IACUC requirements. Pharmaceutical, biotechnology, or CRO experience is highly desirable.
Responsibilities- Independently conduct routine in vivo studies, primarily using CKD and CRM rodent models.
- Assist with design and execution of non-routine and exploratory experiments.
- Perform rodent dosing via i.v., i.p., p.o., s.c., and i.m. routes, along with health monitoring and sample collection.
- Analyze and interpret experimental data; troubleshoot studies and recommend follow-up experiments.
- Maintain accurate records and ensure compliance with IACUC, SOPs, and applicable regulations.
- Conduct literature searches and apply relevant scientific protocols and principles.
- Operate and troubleshoot laboratory equipment.
- Contribute to protocols, procedures, scientific reports, and presentations.
- Maintain high standards of data integrity, scientific ethics, and quality.
- Support adoption of new technologies and collaborate effectively with cross-functional teams.
- Participate in a flexible weekend/holiday rotation as needed; this is not every weekend.
- Bachelor’s degree with 3+ years of relevant experience or Master’s degree in a related scientific discipline. Ph.D. applicants are not eligible.
- Hands-on experience with rodent in vivo research; CKD experience strongly preferred.
- Experience with routine rodent dosing, health monitoring, and sample collection.
- Knowledge of IACUC governance and regulatory compliance.
- Strong problem-solving, troubleshooting, and scientific communication skills.
- Proficiency with Microsoft Excel and Graph Pad Prism; ability to learn additional software.
- Ability to work independently and collaboratively in a fast-paced research environment.
- Pharmaceutical, biotechnology, or CRO experience highly desirable.
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