As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world
Job Summary
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.
You will be responsible for activities ranging from site feasibility and selection, site initiation and start-up, to preparation and conduct of site monitoring, oversight of key performance indicators and site/study close-out.
We offer a competitive salary and extensive benefits package.
Matching Summary
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.
Skills & Requirements
Must-have
GCP and applicable regulations
site feasibility and selection
site initiation and start-up
site monitoring
timely data entry and query resolution
risk-based monitoring model
up to 50% UK-wide travel
Nice-to-have
flexible and independent work
quick learner and problem solver
good communicator and team player
therapeutic area expertise
process improvement participant
Key Requirements
BA or BS degree in Life Sciences, Nursing or related scientific field
Minimum of 2 years of clinical trial monitoring experience
Strong proven understanding of GCP, local laws, and regulations