Excellent interpersonal skills including the ability to interact well with sponsor/client counterparts
Client-focused approach to work
Excellent time management skills
Excellent verbal and written medical communication skills
Excellent standard of written and spoken English
A flexible attitude with respect to work assignments and new learning
Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
Willingness to work in a matrix environment and to value the importance of teamwork.
Qualifications
Experience in clinical medicine (general or specialist qualifications) with Fellowship or specialty training in Ophthalmology, which is expected to be kept up to date.
A background in clinical aspects of drug development, including all aspects of Medical Monitoring and study design/execution, preferred
Clinical practice experience
Good knowledge of the drug development process including drug safety, preferred
Experience in Pharmaceutical Medicine, preferred
Experience leading, mentoring and managing individuals/ a team, preferred
Board certified in Ophthalmology
Experience as a Physician in Industry or as a clinical trial investigator is required
Previous CRO experience is strongly preferred
Medically qualified in an acknowledged medical school with completion of at least basic training in clinical medicine (residency, internship)