Research Scientist/Senior Research Scientist - Acute - Toxicology

As a Toxicology Study Assistant, your role will involve planning, performing, and reporting acute toxicology studies. You will assist in the preparation of SOPs, protocols, and reports, as well as participate in GLP/AAALAC related activities. Your responsibilities will include conducting literature searches, maintaining the animal house and relevant documents in compliance with GLP and AAALAC norms.

Key Responsibilities:

• Collaborate with the Study Director and Technical Coordinator in planning, initiating, and conducting studies
• Administer test items, prepare dose formulations, and collect blood samples
• Assist in data collection, compilation, and verification
• Participate in GLP inspections to ensure regulatory compliance
• Support in interpreting and reporting study data
• Help prepare reports and coordinate activities
• Archive all study-related materials

Qualifications Required:

• 4-8 years of experience in toxicology studies
• Understanding of the agrochemical and pharmaceutical R&D process
• Skills in data interpretation, statistical analysis, laboratory techniques, and experimental design

Additionally, good oral and written communication skills are essential for this role.

Please note that no additional details about the company were provided in the job description. As a Toxicology Study Assistant, your role will involve planning, performing, and reporting acute toxicology studies. You will assist in the preparation of SOPs, protocols, and reports, as well as participate in GLP/AAALAC related activities. Your responsibilities will include conducting literature searches, maintaining the animal house and relevant documents in compliance with GLP and AAALAC norms.

Key Responsibilities:

• Collaborate with the Study Director and Technical Coordinator in planning, initiating, and conducting studies
• Administer test items, prepare dose formulations, and collect blood samples
• Assist in data collection, compilation, and verification
• Participate in GLP inspections to ensure regulatory compliance
• Support in interpreting and reporting study data
• Help prepare reports and coordinate activities
• Archive all study-related materials

Qualifications Required:

• 4-8 years of experience in toxicology studies
• Understanding of the agrochemical and pharmaceutical R&D process
• Skills in data interpretation, statistical analysis, laboratory techniques, and experimental design

Additionally, good oral and written communication skills are essential for this role.

Please note that no additional details about the company were provided in the job description.