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Lead Study Coordinator
2 months ago
Are you driven by the desire to make a significant impact in the field of medicine? Do you recognize that the most valuable asset of any organization is its people? If so, consider the opportunity with our esteemed contract research organization (CRO).
We are a CRO that provides a wide array of services, ranging from serving as an outsourcing partner for early-stage research and development to conducting safety, efficacy, and toxicology assessments for small molecules and advanced therapies. Recently, we have broadened our scope to include manufacturing services for cell, gene, and mRNA-based therapeutics, establishing ourselves as a multifaceted partner in the drug development process.
Our organization consists of three specialized business units located in various regions: our Discovery, Optimization, and Characterization laboratories; our Safety, Efficacy, and Toxicology Site; and our newly established Manufacturing Enablement Center. Each unit is committed to advancing the frontiers of scientific research and development, assisting our clients in bringing transformative therapies to market.
We are currently seeking a Lead Study Coordinator to enhance our expanding team.
As a Lead Study Coordinator, you will manage the scientific aspects of projects, ensuring the effective execution and completion of non-clinical studies. You will evaluate and communicate results to our clients, offer scientific direction to project teams, and collaborate with senior personnel. Your responsibilities will also include drafting study protocols, ensuring adherence to regulatory standards, managing studies within established timelines and budgets, and engaging in continuous improvement initiatives.
Qualifications:
- A Bachelor's degree in a life sciences-related discipline with a minimum of 5 years of experience, a Master's degree with 2 years, or a PhD.
- Experience in a GLP or similarly regulated setting.
- Excellent communication, time management, and organizational abilities.
- Proficiency in the preparation and review of regulatory documentation.
Be part of innovative work that will redefine the future of medicine.
