ื“ืœื’ ืœืชื•ื›ืŸ ื”ืจืืฉื™

๐Ÿš€ Senior Preclinical Scientist | R&D Innovative Biotech (3897)

Gefen Recruitment (ื’ืคืŸ ื”ืฉืžื•ืช)West ื™ืจื•ืฉืœื™ื, ืžื—ื•ื– ื™ืจื•ืฉืœื™ื, ื™ืฉืจืืœืœื ืฆื•ื™ืŸFull-timeื“ืจื’ื”: ืœื ืฆื•ื™ืŸ

ืคื•ืจืกื ืฉืœืฉื•ื ยท 0 ืžื•ืขืžื“ื™ื

ืฉื›ืจ ืœื ืฆื•ื™ืŸ ื‘ืžืฉืจื” ื–ื•

ืฉืžื™ืจื”, ื”ื’ืฉื” ืื• ื‘ื“ื™ืงืช ื”ืชืืžื”. ืคืชื™ื—ืช ื—ืฉื‘ื•ืŸ ื—ื™ื ื ืœื•ืงื—ืช ื›ืžื” ืฉื ื™ื•ืช.

ืชื™ืื•ืจ ื”ืžืฉืจื” ื”ืžืœื

ื”ืžืฉืจื” ื”ืžืงื•ืจื™ืช ยท ื ืฉืžืจ ืœืขื™ื•ืŸ

Join an innovative biotechnology company developing oral peptide therapeutics and help advance breakthrough drug candidates from preclinical research to clinical development.

This is a unique opportunity to become part of a growing R&D team at an exciting stage of the company's journey, with a lead program approaching Phase III clinical trials and additional pipeline programs progressing toward the clinic.

Key Responsibilities:

โ€ข Design, review and oversee preclinical in vivo studies (GLP and non-GLP)

โ€ข Manage CRO collaborations and ensure high-quality study execution

โ€ข Analyze and interpret preclinical data

โ€ข Prepare and author regulatory-grade scientific documentation, including preclinical sections of IND submissions and study reports

โ€ข Support early clinical development activities, including clinical protocols, Investigator's Brochures and Clinical Study Reports

โ€ข Prepare scientific presentations for internal leadership, external partners and scientific meetings

โ€ข Review scientific literature and contribute to cross-functional R&D activities

We're looking for someone with:

โœ” PhD in Pharmacology, Biological Sciences, Bioengineering or a related discipline

โœ” 5+ years of experience in drug discovery and development within the biotech or pharmaceutical industry

โœ” Hands-on experience leading preclinical GLP studies and managing CROs

โœ” Strong scientific writing skills with experience preparing regulatory documentation (IND sections, study reports, regulatory submissions)

โœ” Understanding of early clinical development (Phase Iโ€“II) and global regulatory requirements (FDA, EMA, ICH)

โœ” Excellent communication and presentation skills

โœ” Experience with therapeutic peptides is highly preferred; oral peptide delivery is a significant advantage

ืื•ื“ื•ืช Gefen Recruitment (ื’ืคืŸ ื”ืฉืžื•ืช)
ืคืจื•ืคื™ืœ ื”ื—ื‘ืจื” ยท ื‘ืงืจื•ื‘

ื‘ื™ืงื•ืจื•ืช ืขื•ื‘ื“ื™ื ยท ื‘ืงืจื•ื‘ืขื•ื“ ืžืฉืจื•ืช ื‘-Gefen Recruitment (ื’ืคืŸ ื”ืฉืžื•ืช)

ืฉืืœื•ืช ืขืœ ื”ืžืฉืจื”

  • ื”ืžืฉืจื” ืœื ืฆื™ื™ื ื” ืฉื›ืจ. ืื ื—ื ื• ืžืฆื™ื’ื™ื ืฉื›ืจ ืจืง ื›ืฉื”ืžืขืกื™ืง ืžืคืจืกื ืื•ืชื•.
ื“ื•ืžื•ืช ื•ืงืฉื•ืจื•ืช
Gefen Recruitment (ื’ืคืŸ ื”ืฉืžื•ืช)
ืคื•ืจืกื ืฉืœืฉื•ื ยท 0 ืžื•ืขืžื“ื™ื
ื‘ื“ืงื• ืืช ื”ื”ืชืืžื”