Actalent Nottingham, England, United Kingdom
This is an exciting opportunity with candidates to start at the beginning of January and interview as soon as possible!
The Study Coordinator must have a minimum of 1 year of clinical research experience as they need an individual who can work independently as well as part of a team. Day-to-day responsibilities will involve reporting adverse events, data entry, administrative tasks, and query resolution.
Must have experience:
Oncology
Complex medical understanding
Seniority level
Associate Employment type
Full-time Job function
Research Industries
Pharmaceutical Manufacturing
#J-18808-Ljbffr
Associate Employment type
Full-time Job function
Research Industries
Pharmaceutical Manufacturing
#J-18808-Ljbffr
