Are you passionate about significantly improving the future of medicine? Do you believe that people are the most important asset of any company? If so, join our leading contract research organization (CRO)!

We are a CRO offering a comprehensive range of services, from being an outsourcing partner for discovery stage R&D work, to performing safety, efficacy, and toxicology studies for small molecules and advanced therapies. Recently, we’ve expanded into manufacturing services for cell, gene, and mRNA-based therapeutics, making us a versatile partner in the drug development pipeline.

Our organization is composed of three distinct business units across various locations: our Discovery, Optimization, and Characterization laboratories; our Safety, Efficacy, and Toxicology Site; and our newly opened Manufacturing Enablement Center. Each unit is dedicated to pushing the boundaries of scientific research and development, helping our clients bring life-changing therapies to market.

We are seeking a Study Director to join our growing team!

As a Study Director, you will oversee the scientific elements of projects, ensuring successful implementation and completion of non-clinical studies. You’ll analyze and report results to our clients, provide scientific guidance to project teams, and collaborate with senior staff. Your role will also involve drafting protocols, ensuring regulatory compliance, managing studies within time and budget constraints, and participating in continual improvement initiatives.

What We’re Looking For:

• Bachelor’s degree in a life sciences-related field with 5 years of experience, master’s degree with 2 years, or a PhD.
• Experience working in a GLP or similarly regulated environment.
• Strong communication, time management, and organizational skills.
• Experience in the preparation and review of regulatory documents.

Join our team and be part of groundbreaking work that will change the future of medicine!