As a leading contract research organization (CRO), Labcorp Drug Development (formerly known as Covance) provides comprehensive drug development solutions for a range of industries.
Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services paired with regulatory support for the chemical testing and crop protection industries.
Labcorp Drug Development is a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services.
Our unique perspectives are based on decades of scientific, medical and regulatory expertise.
Role Details :
The "Lead, Global Regulatory Submissions" will be responsible for the timely preparation of submissions to Regulatory Authorities in support of investigational and marketed products.
In this role, you will interact with Regulatory Authorities and with clients to support regulatory activities. You will also interact with internal and external stakeholders to provide guidance regarding Regulatory Authority requirements and project timelines and needs.
Essential Job Duties :
Education, Skills and Other Requirements :
Labcorp is proud to be an Equal Opportunity Employer :
As an EOE / AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.
For more information about how we collect and store your personal data, please see our Privacy Statement.