Experience:
Minimum of 1-2 years of progressive experience in site monitoring within the pharmaceutical, biotechnology, or CRO industry.
Qualification:
Bachelors or advanced degree in a life science discipline.
Skills:
Demonstrated experience as a team player, site monitoring, strong organizational, problem-solving, and interpersonal skills.
Responsibilities:
Overall site management of clinical trials
Coordinate with sites for resolving DCF’s