נכון לתאריך
30/12/2025
רחובות
Ethosia
Description
Responsible for planning and performing pre-clinical studies and supervising pre-clinical CRO's.
Key Responsibilities:
1. Executing in vitro and in vivo pre-clinical projects in-house and via subcontractors in support of company development programs and regulatory submissions.
2. Coordinating the projects timelines and following activities at CROs.
3. Reviewing and performing QC of study plans and reports.
4. Supporting maintenance of animal colonies (transgenic mice, minipigs)
5. Collaboration with clinical and CMC departments to carry out
Qualifications:
1. At least MSc in life sciences or veterinary studies
2. At least 3 years of experience in the biotech industry
3. Experience with performing in vitro and in vivo studies
4. Strong abilities of study analysis (good knowledge in excel and other programs)
5. Strong communication and organizational skills
6. Good level of speaking and writing in English
7. Presentation preparation skills
8. Knowledge of drug development process is a plus
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