Director, Regulatory Affairs - Global Labeling
Gilead SciencesFull Time
Expert & Leadership (9+ years)
Candidates should possess a Bachelor's degree or equivalent, with 0-2 years of relevant experience. This includes effective oral and written communication skills, excellent interpersonal skills, strong attention to detail, good negotiation skills, and proficient computer skills. A basic understanding of medical terminology and regulatory guidelines is also required, along with the ability to work independently or in a team environment.
The Associate Country Approval Specialist will support the preparation, review, and coordination of country and local ethics committee (EC) submissions in alignment with global strategies. This role involves coordinating with internal departments to ensure site start-up activities align with submission timelines, preparing regulatory compliance review packages, and assisting with the development of patient information and informed consent forms. The specialist will also help with grant budget negotiations, maintain trial status information in tracking databases, ensure local country study files are maintained according to SOPs, and stay updated on relevant regulatory guidelines.
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.