ProPharma

Provide high-quality medical information services via phone and email, answering technical product questions professionally. Responsible for identifying and reporting adverse events and translating medical documents between English and Spanish.

Drive excellence in site activities across Europe by managing study coordinators and overseeing project deliverables. Guide research staff on GCP/ICH compliance and manage interactions between the Sponsor and CRO.

The role focuses on driving revenue growth by selling Quality & Compliance solutions and expanding the client base within the life sciences sector. Responsibilities include generating leads, negotiating contracts, writing proposals, and collaborating with internal stakeholders to execute sales strategies.

The role involves responding to medical and safety-related inquiries from healthcare professionals and patients, documenting adverse events, and providing accurate information based on approved resources. Additionally, the specialist will support service quality and contribute to process improvements.

The role involves responding to medical and safety-related inquiries from healthcare professionals and patients, using approved product information to provide accurate responses. Additionally, the specialist will document adverse events and support service quality through checks and training of new team members.