Pharmacovigilance Clinician
Hippocratic AIFull Time
Expert & Leadership (9+ years)
Employment Type: Full time Work Schedule: Standard (Mon-Fri) Environmental Conditions: Office
Reporting to the Pharmacovigilance (PV) Manager, the Safety Administrator (SA) is responsible for providing administrative support to PPD's Global Safety Writing Team responsible for delivering various safety-related documents, including aggregate safety reports, responses to regulatory authority assessment reports, and Risk Management Plans (RMPs).
Working within the pharmacovigilance department, the SA will complete assigned tasks to meet appropriate quality standards and allocated time constraints. In addition to managing the team mailbox and tracking key team- and project-related information, the SA will play a crucial role in assisting authors with the preparation of their deliverables. This includes scheduling meetings, drafting planning documents and data requests, formatting, compiling final documents, filing, and producing compliance metrics.
The ideal candidate will possess a proactive and adaptable attitude, with the ability to prioritize tasks and handle multiple responsibilities. Being able to work as part of a remote team and independently is essential. Additionally, thriving in a fast-paced environment and being receptive to evolving processes is crucial.
Provides life sciences products and services
Thermo Fisher Scientific offers a variety of products and services that support scientific research and healthcare, including laboratory equipment, reagents, and software solutions. Their products are used in applications like protein biology, real-time PCR, and sequencing, serving clients such as academic institutions and pharmaceutical companies. Unlike competitors, Thermo Fisher emphasizes customer support and education, helping clients optimize their experiments. The company's goal is to be a leading provider of life sciences solutions that contribute to a healthier and safer world.