Research Associate I/II – In Vivo Pharmacology

Medicilon USA is seeking a Research Associate I or 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.