Research Associate, In Vivo - Contract - Cambridge, MA
Help bring science to life and join a leading pharmaceutical company to play a key role in delivering impactful research that drives healthcare innovation!
Proclinical is seeking a dedicated Research Associate to join our client's experienced In Vivo Technical Support Team.
Primary Responsibilities:
In this role, you will be responsible for organizing, conducting, and reporting non-GLP rodent toxicology, investigative, and pharmacokinetics-toxicokinetic (PK-TK) studies that support drug discovery and development. This position requires hands-on work with rodents and is based onsite in Cambridge, MA.
Skills & 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.
- Effective written and verbal communication skills within and across teams.
- Physical ability to lift up to 50 lbs, move heavy objects, and stand for prolonged periods while performing repetitive tasks.
- Strong organizational skills, attention to detail, and a sense of personal accountability.
- Commitment to professional development and continuous learning.
The Research Associate's responsibilities will be:
- 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.
- Perform other duties as assigned by the manager.
Compensation:
If you are having difficulty in applying or if you have any questions, please contact Mike Raletz at m.raletz@proclinical.com
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
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