In Vivo Technician
Pfizer Statistics Program
Summary
The In Vivo Technician within the Drug Safety R&D organization is responsible for performing accurate, high quality in-life study work for rodent and non-rodent safety studies in compliance with the study protocol, Standard Operating Procedures (SOPs), Good Laboratory Practice (GLP) regulations, Environmental Health and Safety (EHS) standards, animal welfare regulations, and departmental policies/procedures.
Job description
What You Will Achieve
- Perform assigned in vivo study activities in compliance with applicable regulatory requirements, study protocols, SOPs, and company procedures.
- Support the in-life phase of rodent and non-rodent safety/toxicology studies, including study set-up, test article administration, animal observations, sample collection, data collection, and documentation.
- Read, understand, and follow study protocols and associated Pristima protocols to ensure study activities are performed as required.
- Accurately enter, review, and document study data and correct errors in accordance with established procedures.
- Perform self-review and, as appropriate, peer review of in-life data for accuracy, completeness, and protocol compliance.
- Prepare study materials, forms, labels, supplies, and equipment needed for study activities.
- Use, maintain, and perform required checks or calibrations of laboratory equipment, such as balances and IV pumps.
- Identify and communicate equipment or technical issues and assist with troubleshooting as appropriate.
- Communicate with Study Directors, Management, Comparative Medicine, and support personnel regarding study activities, animal observations, and unexpected findings.
- Follow established animal welfare practices and promptly communicate observations or issues to appropriate personnel.
- Support preparation of study data and documentation for quality assurance review and archiving.
- Manage assigned activities to meet study timelines while maintaining data quality.
- Maintain clean, organized, and safe work areas.
- Participate in departmental training, SOP updates, and continuous improvement activities.
- As training and experience progress, may serve as a Primary Technician for assigned studies.
Minimum Requirements
- High School Diploma or GED with 2+ years of relevant experience
- Demonstrated ability to handle multiple projects simultaneously
- Strong organizational and time management skills
- Detail-oriented with strong interpersonal and communication skills
- Proficiency in using laboratory equipment and software
- Basic understanding of laboratory protocols and procedures
Preferred Requirements
- A Bachelor's Degree
- Experience in a biological laboratory, specifically in vivo work
- Ability to work independently and as part of a team
- Meticulous attention to detail
- Excellent problem-solving abilities
- Strong analytical and critical thinking skills
- Familiarity and basic understanding of common AI tools and a curiosity for learning how they can be used to enhance productivity
Physical/Mental Requirements
Must be able to lift 40 lbs and to stand for at least 3 hours. Must also have the ability to perform mathematical calculations.
Non-Standard Work Schedule, Travel or Environment Requirements
Overtime, weekend and holiday work is required. Work Location Assignment: On Premise.
Requirements
- High School Diploma or GED with 2+ years of relevant experience
- Demonstrated ability to handle multiple projects simultaneously
- Strong organizational and time management skills
- Detail-oriented with strong interpersonal and communication skills
- Proficiency in using laboratory equipment and software
- Basic understanding of laboratory protocols and procedures
- Must be able to lift 40 lbs and stand for at least 3 hours
- Ability to perform mathematical calculations
- Overtime, weekend and holiday work required
- Permanent work authorization in the United States required
Benefits
- 401(k) Matching
- Retirement Savings Contribution
- Paid Vacation
- Paid Holidays
- Paid Personal Days
- Paid Caregiver Leave
- Paid Parental Leave
- Paid Medical Leave
- Medical Insurance
- Prescription Drug Coverage
- Dental Insurance
- Vision Coverage
- Overtime Pay Premiums
Company overview
The Pfizer Statistics Program represents the statistical and data sciences functions within Pfizer Inc., one of the world's premier biopharmaceutical companies. This specialized program encompasses both the statistical analysis capabilities that support Pfizer's drug development pipeline and the educational initiatives like the Breakthrough Fellowship Program that includes MS Statistics components. As part of Pfizer's Research & Development organization, the Statistics Program plays a critical role in clinical trial design, data analysis, regulatory submissions, and evidence generation for Pfizer's innovative medicines and vaccines. The program employs advanced statistical methodologies and data science techniques to ensure the scientific rigor and integrity of Pfizer's clinical research across therapeutic areas including oncology, internal medicine, immunology, and vaccines. Through its integration with Pfizer's global operations, the Statistics Program contributes to the company's mission of delivering breakthroughs that change patients' lives by providing robust statistical support from early discovery through post-marketing surveillance.