In Vivo Scientist II – CKD / CRM

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 Summary Seeking 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. Qualifications 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 GraphPad 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.