USA - Pharmacology Associate - I - USD (contract)

Pfizer; Groton (CT); On-site; USD 34,000 - 40,000; Full time

Benefits offered by this job

Comprehensive benefits

STD/LTD

Life insurance

Job summary

Pfizer in Groton, CT is seeking a Pharmacology Associate I to join an In Vivo Pharmacology team. This on‑site contract role focuses on executing in vivo studies contributing to obesity, metabolic and cardiovascular disease drug discovery, within a collaborative research environment.

The candidate will work with animal models across species, gain exposure to project teams and industry practices, and support translational pharmacology studies in a fast‑paced lab setting.

Qualifications

• Bachelor’s or master’s degree in pharmacology, biology, biomedical sciences, animal science or related field.
• Hands‑on experience conducting in vivo studies in vivarium.
• Experience performing animal research procedures in rodents.
• Willingness to work with large animal species (canine and non‑human primates) with training provided.
• Strong technical laboratory skills and willingness to learn new techniques.
• Ability to work independently and as part of a collaborative team.
• Proficiency with Microsoft Office Suite, particularly Excel.

Responsibilities

• Execute in vivo pharmacology studies for obesity, metabolic and cardiovascular disease research programs.
• Conduct studies across multi‑species platforms (rodents, canines, NHPs) following SOPs and safety guidelines.
• Assist with study execution, data collection, experimental procedures and sample management.
• Perform tissue collection and downstream tissue processing activities.
• Analyze, organize and summarize experimental data using standard scientific software.
• Collaborate with multidisciplinary project teams to support research objectives and program advancement.
• Maintain accurate records, study documentation and data integrity.

Skills

Microsoft Office

Problem solving

Biology

Excel

Education

Bachelor's or Master's degree in related field

Tools

GraphPad Prism

Job description

USA - Pharmacology Associate - I - USD (Contract)

Groton, CT, United States (On-site)

Contract (1 year)

Published 17 hours ago

Microsoft Office

problem - solving

Biology

Excel / PowerPoint/ Microsoft suite

Pharmacology

animal research

Location: Groton, CT
Schedule: Full-time, On-site (5 days/week)
Position Type: Contract

Position Summary

We are seeking a highly motivated Pharmacology Associate I to join an In Vivo Pharmacology team supporting metabolic disease research. This hands‑on laboratory role will focus on executing in vivo studies that contribute to obesity, metabolic, and cardiovascular disease drug discovery programs within a collaborative, cross‑functional research environment.

The ideal candidate will bring strong technical skills in animal research, a commitment to high‑quality science, and an interest in developing within the pharmaceutical and biotechnology industry. This role offers the opportunity to contribute directly to translational pharmacology studies while gaining exposure to project teams, scientific strategy, and industry‑standard research practices.

Key Responsibilities

• Execute in vivo pharmacology studies in support of obesity, metabolic, and cardiovascular disease research programs.
• Conduct studies across multi‑species platforms, including rodents, canines, and non‑human primates, while adhering to institutional SOPs and safety guidelines.
• Assist with study execution, data collection, experimental procedures and sample management.
• Conduct tissue collection and downstream tissue processing activities.
• Analyze, organize and summarize experimental data using standard scientific software tools.
• Collaborate with multidisciplinary project teams to support research objectives and program advancement.
• Maintain accurate experimental records, study documentation and data integrity standards.
• Uphold the highest standards of animal welfare and regulatory compliance, including adherence to institutional IACUC protocols and applicable AAALAC, USDA and OLAW standards.
• Participate in team discussions and contribute to continuous improvement of study workflows and technical capabilities.

Required Qualifications

• Bachelor’s or master’s degree in pharmacology, biology, biomedical sciences, animal science or a related scientific discipline.
• Hands‑on experience conducting in vivo studies and working in vivarium and laboratory environments.
• Experience performing animal research procedures in rodents, including basic handling and technical procedures.
• Willingness and ability to work with large animal species, including canine and non‑human primate models with training provided as appropriate based on experimental needs.
• Strong technical laboratory skills and willingness to learn new techniques.
• Ability to work independently and as part of a collaborative team.
• Strong organisational, communication and problem‑solving skills.
• Proficiency with Microsoft Office Suite, particularly Excel.

Preferred Qualifications

• Demonstrated proficiency in animal handling, restraint, dosing and biospecimen collection across rodents, canines and/or non‑human primates.
• Experience supporting metabolic disease, obesity, cardiovascular disease or related therapeutic areas.
• Prior pharmaceutical, biotechnology or industry research experience.
• Familiarity with GraphPad Prism or similar scientific data analysis software.
• Experience supporting large‑scale preclinical studies.
• Fully on‑site position located in Groton, CT.
• Significant time spent in vivarium and laboratory settings conducting animal studies.
• Work requires adherence to PPE, biosafety, animal welfare and institutional compliance requirements.
• Flexible start times based on study requirements, typically between 7:00 AM and 9:00 AM.
• Occasional weekend work may be required depending on study schedules.
• Overtime eligibility may apply based on business needs.

Ideal Candidate Profile

• The successful candidate will be:
• Technically strong in animal research methodologies with interest in building expertise across multiple species.
• Eager to learn and grow within a research‑driven environment.
• Comfortable working in a highly collaborative, matrixed team structure.
• Self‑motivated and capable of taking ownership of assigned responsibilities.
• Interested in long‑term career development within the pharmaceutical or biotechnology industry.
• Adaptable, dependable and committed to high‑quality scientific work.

Interview Process

• Initial virtual interview with the hiring manager.
• Virtual team interview with members of the research group.
• In‑person interview with the hiring manager, members of the research group and members of the veterinary staff.
• Final selection based on technical qualifications, relevant experience, collaboration style and alignment with role requirements.

This opportunity offers valuable exposure to translational drug discovery research and the potential for long‑term career growth within a dynamic scientific organisation.

Pay Rate Range

• Min Pay Rate $25
• Max Pay Rate $29

Currency USD

Unit hourly

Additional Notes

Please note that contractors are engaged to provide services to Pfizer on a temporary basis in connection with a specific assignment. Contractors are hired and employed through Atrium, our third‑party payrolling partner. This job posting is for a temporary role as an employee of Atrium on assignment at Pfizer. The individual selected for this role will be offered the role as an employee of Atrium; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by Atrium upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job‑related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements.

Benefits Information

• Comprehensive Benefits Package available based on eligibility
• Short‑Term Disability (STD)
• Long‑Term Disability (LTD)
• Supplemental and Voluntary Life Insurance