Pharmacovigilance Clinician
Hippocratic AIFull Time
Expert & Leadership (9+ years)
Philippines
The ideal candidate will have experience in pharmacovigilance or a related field, with a strong understanding of safety and regulatory publishing documents. Familiarity with electronic trial master files, IT security standards, and data privacy regulations is necessary. Experience with data entry, budget management, and expense oversight is also required.
The Pharmacovigilance Coordinator will coordinate the review of safety and regulatory publishing documents, ensuring quality and compliance with internal systems and electronic trial master files. Responsibilities include maintaining licenses, facilitating project meetings, managing project-specific training and files for audit readiness, and performing data entry and system reconciliations. The role also involves identifying and redacting confidential information, managing expenses and translations, and archiving regulatory publishing documents and submissions.
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.