USA - Pharmacology Associate - I - USD (contract)

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

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Short-Term Disability

Long-Term Disability

401(k)

Job summary

Pfizer in Groton, CT, seeks a Pharmacology Associate I for a fully on-site contract role in an In Vivo Pharmacology team. You will execute in vivo studies across obesity, metabolic, and cardiovascular programs and work with rodents, dogs, and non-human primates under SOPs.

The ideal candidate has a degree in pharmacology or related fields and hands-on vivarium experience, with strong data handling and collaboration skills. Flex start times and potential overtime may apply.

Qualifications

• Hands-on in vivo pharmacology experience required.
• Experience in vivarium and laboratory environments.
• Familiarity with multi-species animal studies is preferred.

Responsibilities

• Execute in vivo pharmacology studies supporting obesity, metabolic, and cardiovascular programs.
• Conduct studies across rodents, canines, and non-human primates per SOPs.
• Assist with study execution, data collection, and sample management.
• Maintain accurate records and ensure regulatory compliance.

Skills

In vivo pharmacology

Animal research

Multi-species studies

Attention to detail

Communication skills

Excel

Education

Bachelor’s or Master’s degree in pharmacology/biological sciences

Tools

GraphPad Prism

Job description

Pharmacology Associate I

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 organizational, 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.

Work Environment

• 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 organization.

Pay Rate Range

25 - 29 USD 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

• Medical, Dental, Vision
• Short-Term Disability (STD)
• Long-Term Disability (LTD)
• Supplemental and Voluntary Life Insurance
• 401(K)
• Commuter Benefit Program