More jobs:
Scientist II
Job in
Ridgefield, Fairfield County, Connecticut, 06879, USA
Listed on 2026-07-10
Listing for:
System One
Full Time, Per diem
position Listed on 2026-07-10
Job specializations:
-
Research/Development
Research Scientist, Medical Technologist & Lab Technician, Clinical Research, Medical Science -
Healthcare
Medical Technologist & Lab Technician, Clinical Research, Medical Science
Job Description & How to Apply Below
Scientist II
Location:
Ridgefield, CT
Type:
Contract
Compensation: $30 -$40.00
Contractor Work Model:
Onsite
Hours:
40 hrs/week
Overview
Leading pharmaceutical company looking for an experienced Scientist II. Ideal candidates should have a Master's Degree with 2-3 years experience or Bachelor's Degree with 3+ years experience in related scientific discipline; pharmaceutical, biotechnology or CRO experience is highly desirable; non-PhD applicant required.
Responsibilities
+ Independently initiates and completes routine in vivo studies efficiently, with minimal supervision. Interprets experimental outcomes and recommends appropriate follow-up.
+ Demonstrates technical proficiency supporting the development and validation of rodent models for cardiometabolic diseases.
+ Applies basic scientific principles with minimal guidance; performs literature searches and extracts relevant information from published protocols.
+ Proposes new ideas and technologies, builds support, and implements improvements based on scientific and technical expertise and an understanding of the drug discovery and development process.
+ Independently operates and maintains laboratory equipment and troubleshoots issues effectively.
+ Communicates work effectively, both orally and in writing; contributes to protocols, procedures, and technical reports; and provides input for scientific reports.
+ Records, analyzes, and reports data with a high level of integrity and ethical conduct.
+ Complies with applicable regulations and performs all work safely; maintains accurate records in accordance with Standard Operating Procedures and policies.
+ Contributes to design and execution of in vivo studies relevant to cardio-renal metabolic diseases (kidney injury, cardiovascular and metabolic driven cardio-renal dysfunction).
+ Performs dosing procedures (oral gavage, IP/IV/SC injections), physiological monitoring, and sample collection (blood, urine, tissues).
+ Conducts functional assessments, such as blood pressure measurements, echocardiography support, telemetry, metabolic cage studies, and renal function assays.
+ Processes and analyzes biological samples, including histology, biomarker assays, qPCR, ELISA, and other molecular or biochemical readouts.
+ Maintains high-quality documentation, including study protocols, animal records, raw data, and reports compliant with internal and regulatory standards.
+ Collaborates cross functionally with pharmacology, pathology, bioanalytics, and therapeutic area biology teams to interpret data and refine study designs.
+ Ensures compliance with IACUC protocols, ethical animal care standards, and institutional guidelines.
+ Contributes to scientific discussions, presents data at team meetings, and supports preparation of internal reports and external publications.
+ Requires moderate physical activity to perform work in the vivarium and laboratory, including standing for extended durations, working under a biosafety hood, bending, lifting up to 20 lbs, squatting, pushing/pulling, and reaching.
+ Requires daily handling and restraint of small laboratory animals (rats, mice; 50 at a time), often within a specified timeframe.
+ Requires use of personal protective equipment (PPE), including respiratory, eye, hand, and foot protection.
+ Ability and willingness to work effectively in a highly collaborative environment and support weekend work as needed.
+ Strong communication skills and ability to work collaboratively in a fast-paced research environment.
Requirements
+ Master's Degree with 2-3 years experience or Bachelor's Degree with 3+ years experience in related scientific discipline; pharmaceutical, biotechnology or CRO experience is highly desirable; non-PhD applicant required.
+ Understanding of physiology, pharmacology, and disease mechanisms relevant to cardio-renal biology.
+
Experience with dosing procedures (oral gavage, IP/IV/SC injections), physiological monitoring, and sample collection.
+ Proficiency in processing and analyzing biological samples, including histology, biomarker assays, qPCR, ELISA, and other molecular or biochemical readouts.
+ Strong documentation skills,…
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