Kailera Therapeutics is a biotech company developing advanced therapies for obesity and related conditions. Their lead product, KAI-9531 (HRS9531), an injectable GLP-1/GIP receptor dual agonist, has shown positive results in Phase 2 trials. The company also advances a diversified pipeline with oral administration options. Kailera's mission is to provide transformative weight management solutions that enhance overall health.
Open Positions
Associate Director, CMC Operations
10+ years of experience in pharmaceutical drug development, excellent communication skills, and proficiency in Smartsheet software are required
Associate Director, Analytical Development and Quality Control
10+ years of experience, or 5+ with advanced degree, in the pharmaceutical/biotech industry with experience in all phases of innovative drug development and commercial launch
Director, Corporate Communications
10+ years of experience in corporate communications, strong writing and project management skills, and a bachelor’s degree in Communications, Business, or a related field
Senior Manager, CMC Operations
8+ years of experience, excellent communication skills, and proficiency in Smartsheet software required
Associate Director, Clinical Data Management
10+ years of experience in clinical data management and knowledge of FDA and ICH/GCP regulations
Senior Clinical Trial Manager
8+ years of clinical trial experience, including direct management of CROs and vendors
Medical Director, Clinical Development
2+ years of industry experience in clinical development, hands-on experience designing and executing clinical trials, and understanding of GCP, clinical trial design, regulatory requirements, and safety monitoring
Senior Director, KAI-9531 Global Brand Lead
10+ years of experience in pharmaceutical marketing, launch experience, and a proven track record of building global pharmaceutical brands
Associate Director, Pharmacovigilance Scientist
5-7 years of experience in global pharmacovigilance, safety data analysis, signal management, and benefit-risk evaluation, and an advanced degree (PharmD, MS, NP, RN) or equivalent
Senior Director, Drug Substance Development and Manufacturing (Peptide)
10+ years of experience in drug substance development and manufacturing, hands-on experience with peptide synthesis and manufacturing, and a demonstrated track record in managing clinical-scale supply and process validation activities
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