
Research Professional
Há 13 horas
Key responsibilities include identifying and initiating investigational sites, monitoring studies to ensure compliance with protocols and regulations, providing mentorship to colleagues, recognizing and adhering to company values, traveling extensively, maintaining knowledge of SOPs and regulations, managing study setup activities, ensuring accurate data entry and documentation, handling investigational product storage and management, participating in study documentation and training, and contributing to cost management efforts.
Requirements:- Bachelor's degree in a health or science field.
- Minimum 2 years clinical trial monitoring experience.
- Strong knowledge of ICH GCP, SOPs, local laws, and protocols.
- Proficiency with relevant software and systems.
- Ability to travel as required.
This is an exciting opportunity to join a global clinical research organization and contribute to the development of new treatments and therapies.
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