Scientist - In Vitro Global Safety Pharmacology
Net2Source Inc. · Groton, CT
CONTRACT
Posted Sep 9, 2026
Job Description
Job title: Scientist - In Vitro Global Safety Pharmacology
Location – Groton CT
Duration: 12+ Months
Role Description:
This position will be responsible for supporting drug discovery by performing in vitro experiments to assess the off-target pharmacology of novel compounds using both cellular and biochemical assays.
Responsibilities:
Work independently and as part of a team to help design, execute, analyze / interpret data generated from experiments from biochemical and in vitro cell-based assays.
Specific duties to include:
● Apply scientific knowledge in running early in-vitro safety screening assays (384 well plate based; medium throughput) using a range of in vitro cell based, enzyme assays and transporter assays.
● Support screening efforts by performing aseptic cell culture work for multiple cell lines.
● Keep detailed experimental records and prepare study summaries and technical reports.
● Have a working knowledge of analysis tools such as Excel, GraphPad Prism, and PowerPoint for experimental documentation and data analysis/presentations.
● Contribute to building an innovative culture that embraces scientific excellence, urgency, partnerships with key stakeholders, continuous learning and improvement, increasing technical skill base and in vitro expertise.
Basic Qualifications:
● Bachelor's degree plus 5 years pertinent laboratory experience in Pharmacology (or related field).
● Previous experience running cell/enzyme-based assay platforms in a medium to high throughput environment is required. Experience using plate-based instrumentation (liquid handling, fluorescent plate readers, plate-based scintillation counters)
● Cell culture experience
● Eagerness to learn new laboratory techniques
● Ability to work in fast paced environment and meet deadlines.
● Strong organizational, interpersonal and communication skills as well as ability to perform tasks with minimal supervision. Team player attitude is a must.
● Excellent time-management skills and ability to follow pre-established experimental designs and troubleshoot problems in an independent manner.
Preferred Qualifications:
● Working knowledge of receptor pharmacology principles
● Experience with Molecular Devices FLIPR, Revvity Envision and Envision Nexus, Perkin Elmer Microbeta2 platforms
● Experience using Revity Signals Electronic Notebook
Location – Groton CT
Duration: 12+ Months
Role Description:
This position will be responsible for supporting drug discovery by performing in vitro experiments to assess the off-target pharmacology of novel compounds using both cellular and biochemical assays.
Responsibilities:
Work independently and as part of a team to help design, execute, analyze / interpret data generated from experiments from biochemical and in vitro cell-based assays.
Specific duties to include:
● Apply scientific knowledge in running early in-vitro safety screening assays (384 well plate based; medium throughput) using a range of in vitro cell based, enzyme assays and transporter assays.
● Support screening efforts by performing aseptic cell culture work for multiple cell lines.
● Keep detailed experimental records and prepare study summaries and technical reports.
● Have a working knowledge of analysis tools such as Excel, GraphPad Prism, and PowerPoint for experimental documentation and data analysis/presentations.
● Contribute to building an innovative culture that embraces scientific excellence, urgency, partnerships with key stakeholders, continuous learning and improvement, increasing technical skill base and in vitro expertise.
Basic Qualifications:
● Bachelor's degree plus 5 years pertinent laboratory experience in Pharmacology (or related field).
● Previous experience running cell/enzyme-based assay platforms in a medium to high throughput environment is required. Experience using plate-based instrumentation (liquid handling, fluorescent plate readers, plate-based scintillation counters)
● Cell culture experience
● Eagerness to learn new laboratory techniques
● Ability to work in fast paced environment and meet deadlines.
● Strong organizational, interpersonal and communication skills as well as ability to perform tasks with minimal supervision. Team player attitude is a must.
● Excellent time-management skills and ability to follow pre-established experimental designs and troubleshoot problems in an independent manner.
Preferred Qualifications:
● Working knowledge of receptor pharmacology principles
● Experience with Molecular Devices FLIPR, Revvity Envision and Envision Nexus, Perkin Elmer Microbeta2 platforms
● Experience using Revity Signals Electronic Notebook
Additional Details
- City
- Groton
- State
- Connecticut
- Country
- US
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