02 nov
|
Fortrea
|
Tandil
Fortrea is seeking a regulatory submissions specialist to serve as primary contact with investigative sites, manage regulatory documents, and ensure timely submissions under ICH/GCP guidelines.The role involves coordinating with senior staff, vendors, and study teams to maintain compliance across country-specific requirements and prepare documents for IRB/IEC submissions, with emphasis on accuracy and timeliness.#J-18808-Ljbffr
📌 Regulatory Start-Up Associate, Clinical Trials (Tandil)
🏢 Fortrea
📍 Tandil