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Research Associate II In Vivo Pharmacology
Lexington, MA, 02421, USPosted 1 weeks ago
Full-timeonsite
Job Description
Medicilon USA is seeking a Research Associate II to support the execution of preclinical in vivo pharmacology and disease model studies. The successful candidate will have hands-on experience conducting rodent studies in a CRO, biotechnology, or pharmaceutical environment and will be responsible for study execution, animal procedures, sample collection, and data documentation.
This position works closely with study scientists and project teams to ensure high-quality study conduct, adherence to timelines, and compliance with animal welfare and regulatory requirements.
Key Responsibilities
- Perform routine animal handling, restraint, dosing, monitoring, and sample collection activities in rodent models.
- Prepare test article formulations and perform dose calculations according to study protocols.
- Administer compounds through common routes including oral gavage, intravenous (IV), subcutaneous (SC), and intraperitoneal (IP) administration.
- Conduct blood collection, tissue collection, necropsy, and other study-related procedures.
- Perform protocol-specific assessments, including body weight collection, clinical observations, disease scoring, and other in-life measurements.
- Support study initiation activities, including preparation of study materials, labeling, room setup, and protocol review.
- Accurately record procedures, observations, and study data in laboratory notebooks, electronic systems, and study records.
- Ensure studies are conducted in accordance with approved protocols, IACUC requirements, SOPs, and company policies.
- Monitor animal health and welfare throughout study conduct and promptly communicate concerns to study management and veterinary staff.
- Maintain laboratory equipment, supplies, and inventory required for study execution.
- Collaborate effectively with scientists and cross-functional teams to support project timelines and deliverables.
- Participate in training activities and continuously develop technical skills and knowledge.
- Perform all activities in compliance with applicable regulations, company policies, and training requirements.
- Other duties and responsibilities as assigned.
Qualifications
Required:
- Bachelor's degree in Biology, Animal Science, Life Sciences, or a related scientific discipline.
- 1–3 years of hands-on in vivo experience in a CRO, biotechnology, pharmaceutical, or related industry environment.
- Experience with rodent handling, restraint, dosing, and animal monitoring.
- Experience administering compounds through common routes including oral gavage, intravenous (IV), subcutaneous (SC), and intraperitoneal (IP) injection.
- Experience with blood collection, tissue collection, necropsy, and sample processing.
- Experience executing studies according to protocols, SOPs, and regulatory requirements.
- Familiarity with IACUC requirements and animal welfare regulations.
- Experience supporting pharmacology, efficacy, or disease model studies.
- Strong attention to detail and ability to maintain accurate study documentation.
- Ability to manage multiple priorities and work effectively in a fast-paced team environment.
- Strong communication and organizational skills.
Preferred:
- ALAT certification or equivalent laboratory animal training.
- Experience working in a GLP-regulated environment.
- Experience with immunology, inflammation, metabolic disease, or other therapeutic areas.
- Experience with additional in vivo techniques such as PK sampling, telemetry, surgical support, or specialized model assessments.