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Actalent Clinical Regulatory Associate (Hybrid) in Charlotte, North Carolina

The Regulatory Associate is responsible for regulatory compliance clinical trials performed by the assigned disease group. The position requires that the person be responsible for IRB submissions and responses and for creating and maintaining professional working relationships with investigators, sponsors, team members, and others.

Requirements:

*1+ years handling,

reviewing, and submitting Regulatory Documents for Clinical trials (site level)

*4 year degree Preferred: Oncology Experience

Location: Chapel Hill, NC

Mostly home based, 2-3 days on site per month Equipment (laptop, monitors) are provided by UNC

About Actalent:

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

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