About Celerion
Accelerating drug development with reliable research data
Key Highlights
- Over 40 years of experience in early phase research
- Headquartered in Lincoln, Nebraska
- Serves major clients including Pfizer and Merck
- Employs between 251-1,000 professionals
Celerion, headquartered in Lincoln, Nebraska, has over 40 years of experience in early phase drug development, providing critical data to pharmaceutical companies. With a focus on accelerating drug development, Celerion offers services such as bioanalytical testing and clinical trial management, ser...
🎁 Benefits
Celerion offers competitive salaries, comprehensive health benefits, a 401(k) plan with company match, generous PTO, and opportunities for remote work...
🌟 Culture
Celerion fosters a culture of speed and reliability, emphasizing data-driven decision-making and a commitment to scientific excellence. The company va...
Overview
Celerion is hiring a Bioanalytical Principal Investigator to oversee the bioanalytical portion of clinical studies. This role is based in Lincoln, NE, and requires expertise in bioanalytical methods for large molecules.
Job Description
Who you are
You have extensive experience in bioanalytical methods, particularly in ligand binding assays, and have a proven track record of leading research projects in a clinical setting. Your expertise allows you to ensure the technical conduct of studies meets regulatory standards and scientific rigor. You are adept at collaborating with cross-functional teams, including clinical operations and regulatory affairs, to drive projects forward. Your strong communication skills enable you to present complex data clearly to stakeholders and contribute to scientific publications.
You are passionate about advancing clinical research and are motivated by the opportunity to contribute to the development of life-saving treatments. You thrive in a fast-paced environment and are committed to maintaining high-quality standards in your work. Your leadership skills allow you to mentor junior scientists and foster a collaborative team culture.
What you'll do
As a Bioanalytical Principal Investigator, you will be responsible for the overall technical conduct of the bioanalytical portion of studies, ensuring compliance with regulatory requirements and scientific integrity. You will lead the design and validation of bioanalytical methods, particularly for large molecules, and oversee the execution of these studies. Your role will involve collaborating with project teams to define study objectives and timelines, as well as providing guidance on data interpretation and reporting.
You will also be responsible for managing resources and budgets associated with bioanalytical studies, ensuring that projects are completed on time and within scope. Additionally, you will contribute to the preparation of regulatory submissions and scientific publications, showcasing the results of your team's work. Your leadership will be crucial in driving innovation within the bioanalytical team and enhancing the overall capabilities of the organization.
What we offer
Celerion offers a dynamic work environment where you can make a significant impact on clinical research. You will have the opportunity to work with a talented team dedicated to advancing drug development. We provide competitive compensation and benefits, as well as opportunities for professional growth and development. Join us in our mission to bring life-saving treatments to market faster.
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