In Vivo Assistant Job at AbCellera Biologics (Vancouver)

Laboratory Operations Assistant - In Vivo Models

From target to the clinic. AbCellera’s platform integrates biology, computation,...

Location

Canada , Vancouver

Salary:

50000.00 - 61600.00 CAD / Year

AbCellera Biologics

Expiration Date

Until further notice

Requirements

Able to work autonomously and take pride in being self-motivated
Thrive in a collaborative, fast-paced work environment with multiple competing priorities
At least 1 year of experience working in a research environment, preferably in vivo
A fast learner, team player, and creative problem solver
Excellent communication, documentation, and organizational skills, and are known for accountability and reliability
Able to lift up to 25 kg, and are comfortable with long periods of standing and bending throughout the day

Job Responsibility

Maintaining the lab space and restocking supplies for in vivo, in vitro, and ex vivo activities
Assisting in the preparation of materials for laboratory experiments
Ordering and organizing the distribution of materials to the central lab and storage locations using an inventory management system
Performing daily cage wash operations, including sterilization, and disposal of non-hazardous and hazardous waste
Preparing cleaned cages with sterile bedding and enrichment items
food and water
Using laboratory glassware washers, autoclaves and ovens to clean and sterilize laboratory glassware and other labware
Preparing, labelling and aliquoting common reagents, animal diet food and treats
Transporting of samples between sites across Vancouver
Maintaining core lab equipment: freezers, pipettes and incubators

What we offer

Equity
Annual bonus dependent on team and company performance
6% (non-match) RRSP contribution
CAD $1,500 annual Active Lifestyle Allowance
Annual vacation
Opportunity for flexible work arrangements
Professional development opportunities
Comprehensive health benefits
Scientific and technical mentorship
Teams and social groups to build community and connections

Fulltime

Senior Associate (In Vivo Pharmacokinetics and Drug Metabolism)

We are seeking a highly motivated, detail-oriented, and collaborative Senior Ass...

Location

United States , Thousand Oaks

Salary:

79424.85 - 107457.15 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Master's degree
Bachelor's degree with a minimum of 2 years of rodent laboratory animal research experience
Associate's degree with a minimum of 4 years of rodent laboratory animal research experience
High school diploma / GED with a minimum of 6 years of rodent laboratory animal research experience

Job Responsibility

Support senior team members in the execution of preclinical in vivo PKDM-BA studies using mouse and rat models
Assist with routine handling, restraint, husbandry support, and dosing of mice and rats through multiple administration routes including intravenous (IV), oral gavage (PO), subcutaneous (SC), and intraperitoneal (IP)
Perform biological sample collection from rodents including blood, plasma, serum, urine, feces, and tissue specimens under the guidance of experienced scientists and study leads
Conduct clinical observations, monitor rodent health and welfare, and accurately document findings in accordance with study protocols and institutional guidelines
Support rodent necropsy procedures, tissue collection and processing, and basic surgical manipulations as directed by senior staff
Prepare study materials, dosing formulations, laboratory supplies, and associated documentation to facilitate efficient study execution
Maintain accurate, organized, and compliant experimental records and laboratory documentation
Assist with laboratory organization, equipment readiness, and inventory management of research consumables and animal study supplies
Adhere to institutional animal care and use guidelines, SOPs, and laboratory safety procedures
Collaborate effectively with scientists, veterinarians, and laboratory staff to support research timelines and study objectives

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Fulltime

Research Associate, In Vivo

Help bring science to life and join a leading pharmaceutical company to play a k...

Location

United States , Cambridge

Salary:

36.00 - 40.00 USD / Hour

Proclinical

Expiration Date

Until further notice

Requirements

Background in biology or a related field, with hands-on experience in laboratory rodent research
Proficiency in dose administration techniques for rats and mice (e.g., SC, IV, PO, IT, IM)
Skilled in blood collection methods (e.g., tail vein, submandibular, terminal collection)
Ability to identify and document abnormal behavior and clinical signs in rodents
Strong mathematical skills for calculating dilutions and dose projections
Proficiency in MS Word, Excel, PowerPoint, and GraphPad Prism
experience with electronic data capture systems is a plus
Knowledge of rat and mouse anatomy for necropsies and tissue collections
Familiarity with applicable Animal Welfare Guidelines
Certification as an Assistant Laboratory Animal Technician (ALAT) or Laboratory Animal Technician (LAT) is advantageous

Job Responsibility

Coordinate pre-study activities, including protocol development, test article procurement, and animal ordering
Perform dose calculations and prepare dosing solutions
Conduct study procedures such as dosing, monitoring clinical signs, recording body weights, collecting blood samples, performing necropsies, and tissue collections on mice and rats
Utilize Excel spreadsheets or electronic data capture systems to collect and manage study data
Perform quality control checks on study data
Draft initial study reports and collaborate with Principal Investigators to finalize them
Create graphs of key study parameters using Excel or GraphPad Prism
Communicate effectively in group meetings and research discussions, while managing conflicts professionally
Maintain a safe and clean working environment by adhering to procedures, rules, and regulations
Adapt quickly to changing priorities in a dynamic work environment

Nuclear Med Technologist II

As our Nuclear Med Tech II, you will be a specialized healthcare professional, v...

Location

United States , Bryan

Salary:

39.08 - 58.14 USD / Hour

American Nursing Care

Expiration Date

Until further notice

Requirements

Three (3) years Nuclear Medicine experience
Medical Radiographer: TX (MRT)
One of the following: Certified Nuclear Medicine Technologist (CNMT) or Registered Technologist Nuclear Medicine Technology (RTNM)
Basic Life Support - CPR, within 14 days of hire

Job Responsibility

Demonstrates mastery of all Nuc Med Tech I Accountabilities/Responsibilities and has completed a minimum of 1 year service in the Nuc Med Tech I position
Performs in‐vitro/in‐vivo studies as outlined in the nuclear medicine procedure manuals
Makes determinations of the validity of the data collected before submission for interpretation
Mentors new employees and students on the proper use of the camera/computer systems, study procedures
Appropriately and professionally reacts to process or procedure deviations
Assists with the formal clinical/technical education process of the department by preparing and presenting 2 staff in‐services per year on a topical subject
Independently performs all Functions regarding the safe and compliant operation of the radiopharmacy and all associated documentation
Educates and mentors qualified staff on proper radio, pharmacy procedures

What we offer

medical
prescription drug
dental
vision plans
life insurance
paid time off (full-time benefit eligible team members may receive a minimum of 14 paid time off days, including holidays annually)
tuition reimbursement
retirement plan benefit(s) including, but not limited to, 401(k), 403(b), and other defined benefits offerings

Fulltime

Scientist Bioanalytics & Pharmacokinetics

Location: Heidelberg, Germany (on site) Start Date: October 2026 Responsibilit...

Location

Germany , Heidelberg

Salary:

Not provided

VERAXA Biotech GmbH

Expiration Date

Until further notice

Requirements

Ph.D. in Life Sciences, Bioengineering, Pharmacology or related subject area with 3+ years of pharmaceutical development experience in pharma, biotech, or a CRO, with a focus on pharmacokinetics and bioanalytics
Experience with designing, optimizing, qualifying, and validating bioanalytical assays using ECL-based immunoassays (Meso Scale Discovery) and ELISA platforms to support PK/TK assessments, including solid understanding of respective regulatory guidelines
Strong laboratory skills, including the ability to independently execute the bioanalysis of primary samples, handling of biological fluids/matrices (biosafety level S1+ S2) and training of technical assistants in respective assays
Experience in maintaining laboratory notebooks and conducting data-fitting using commercially available software packages such as GraphPad Prism
Training in PK data analysis and interpretation and PK/PD modeling, using industry standard software packages e.g. Phoenix WinNonlin
Excellent verbal & written communication and presentation skills
Commitment to fostering a strong quality-driven culture
Fluency in English (spoken and written) is required
Knowledge in R would be beneficial
German skills are a plus

Job Responsibility

Support anti-idiotypic antibody generation at external CROs and characterization efforts
Plan, conduct, evaluate, and qualify bioanalytical assays (focus on ligand binding assays) in-house, at the highest level of scientific integrity
Arrange assay transfers to clinical CROs and validate methods according to regulatory standards for use in FIH studies
Support in the design and interpretation of external non-clinical in vivo PK studies (GLP and non-GLP) for large molecule drug candidates (ADCs and TCEs)
Apply PK and PBPK models using in vivo study data from different species, employing industry-standard software
Prepare expert reports, scientific documents, and presentations in English
Work collaboratively within project teams and communicate efficiently with multidisciplinary teams to design and prosecute studies in line with the strategic direction of the projects

Fulltime

Research Scientist II - Toxicology

We are looking for a dynamic and detail-oriented Research Scientist II to join o...

Location

Canada , Vancouver

Salary:

100000.00 - 125000.00 CAD / Year

AbCellera Biologics

Expiration Date

Until further notice

Requirements

PhD in Toxicology or related biological science field and a minimum of 2-5 years of related experience in an academic or industry environment
candidates with a MSc and 7+ years of relevant experience will also be considered
hands-on experience with in vitro and/or in vivo toxicology studies
strong desire to learn and develop proficiency with nonclinical safety assessment of large molecules/biologics
strong analytical and problem-solving skills
excellent communication and collaboration skills

Job Responsibility

Designing, planning, and supporting the execution of in vitro and/or in vivo toxicology studies as needed, adhering to the appropriate regulatory guidelines and communicating toxicology study results internally
Updating and maintaining proper recording of nonclinical safety study data, as required by Good Laboratory Practice (GLP)
Assisting with the authoring of toxicology sections of Regulatory documentation
Collaborating with scientists across various teams at AbCellera to ensure high data quality and that studies meet the company’s objectives
Contributing to the development of our toxicology programs and participating as a nonclinical safety/toxicology representative as needed
Maintaining an active scan of published toxicology data relevant to AbCellera’s product portfolio, and continuously expanding your knowledge base

What we offer

Equity
annual bonus dependent on team and company performance
6% (non-match) RRSP contribution
CAD $1,500 annual Active Lifestyle Allowance
annual vacation
professional development opportunities
comprehensive health benefits
scientific and technical mentorship

Fulltime

Nuclear Medicine Technologist

As our Nuclear Medicine Technologist, you will be a specialized healthcare profe...

Location

United States , Houston

Salary:

41.14 - 61.20 USD / Hour

American Nursing Care

Expiration Date

Until further notice

Requirements

Completion of an accredited nuclear medicine technology program, upon hire or
Medical Radiographer: TX, upon hire and
Certified Nuclear Medicine Technologist, upon hire or
Registered Technologist Nuclear Medicine Technology, upon hire and
Basic Life Support (BLS) Certification issued by the American Heart Association, upon hire

Job Responsibility

Utilizes innovative customer service techniques to provide a positive patient care experience for the patient and their family
Acts professionally in all dealings with internal and external customers to promote a working environment that focuses on the patient experience and not operational rivalries or roadblocks to care
Establishes and maintains lines of communication with all other staff members and radiologists to ensure an effective and harmonious working environment
Communicates effectively with patients and their families about the procedure to be performed in order to obtain information and to offer reassurance
Coordinate and participate in a variety of technical procedures to include in vivo and in vitro studies
operate radiation detection and measurement instrumentation including stationary imaging devices, scintillation gamma and apparatus for in vitro counting
Calibrate and draw up radiopharmaceutical materials for administration to patients
formulate radiopharmaceutical materials from pre-prepared kits
Calibrate instruments and review calibration data to detect trends indicating instrument malfunction
Calculate data to include results of patient studies and radioactive decay

What we offer

medical plan
prescription drug plan
dental plan
vision plans
life insurance
paid time off (full-time benefit eligible team members may receive a minimum of 14 paid time off days, including holidays annually)
tuition reimbursement
retirement plan benefit(s) including, but not limited to, 401(k)
403(b)
other defined benefits offerings

Fulltime

InVivo Sr. Research Associate

We are seeking a highly motivated and technically skilled Research Associate to ...

Location

United States , Cambridge

Salary:

Not provided

Beacon Hill

Expiration Date

Until further notice

Requirements

B.S. or M.S. in Cell Biology, Immunology, Regenerative Medicine, or a related discipline
3-5+ years of relevant industry experience (Biotech/Pharma experience preferred)
Proficiency in rodent handling, multiple routes of administration (IV, IP, SC), and tissue dissection is required
Hands-on experience with the isolation and culture of primary human cells or tissues is preferred
Strong experience with Flow Cytometry, qPCR, and microscopy
Ability to analyze data statistically and troubleshoot experimental variances independently
Excellent oral and written communication skills
Must be able to structure tasks, set priorities, and work effectively in a collaborative, team-oriented environment

Job Responsibility

Execute in vivo studies using mouse models, including dosing, monitoring, and tissue collection at necropsy
Perform standard dosing and sampling techniques, including SC, IM, IV (retro-orbital), and IP injections, as well as submandibular bleeds and tail nick
Conduct or assist with small rodent surgical procedures (e.g., tissue transplantation/implantation)
Perform specialized tissue processing and imaging techniques, including immunohistochemistry (IHC) and immunofluorescence (IF) staining
Assess in vivo functionality, safety, and tumorigenicity of stem cell-derived cell product
Maintain and expand primary cell cultures using aseptic technique
Perform cell isolation from primary human or mouse tissues for downstream analysis
Conduct downstream biological assays to validate cell quality and function, including Flow Cytometry (FACS), RT-qPCR, and ddPCR, MSD/ELISA
Analyze biomarkers and signalling pathways to correlate in vitro characteristics with in vivo outcomes
Analyze complex datasets using statistical software (e.g., GraphPad Prism) and present findings to the scientific team

Fulltime

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In Vivo Assistant

Job Description

Job Responsibility

Requirements

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