Chief Medical Officer - London, United Kingdom - Grand Pacific CRO
Description
About Us:
The Grand Pacific CRO team has over 25 years' experience in conducting clinical trials in the Asia Pacific region, including Australia, New Zealand and South Africa.
We have continued as a leader in the industry and have expanded services to include central laboratory, site management and image reading services.
We pride ourselves on meeting customers where they are and providing exactly what they need to move their products forward.
Measurement:
- Quality of relationships with and feedback from internal and external stakeholder
- Board feedback
- Successful audit outcomes
- Compliance with regulatory requirements
- Evidence of a 'quality' culture
Responsibility:
- Attending executive level meetings related to the current and future direction of the company.
- Acting as a spokesperson for the Company
- Keeping current medical staff up to date on the changing health regulations
- Providing clinical guidance to physicians
- Overseeing and providing medical monitoring services
- Implementing policy changes and quality improvements
- Assisting with budgets
- Fostering professional relationships
- Advising Medical Liaison teams
- Participating in strategy teams to provide advice and direction, including identifying and assessing risk.
- Participating with Regulatory in developing potential clients via expert commentary on medical safety matters
Delivery:
- Good quality, safe and effective clinical trials
- Medical staff who are up to date on the changing health regulations globally
- Clinical guidance to physicians
- Medical monitoring services
- Policy changes and quality improvements.
- Building excellent relationships with professional stakeholders
Qualifications
- Medically qualified
- MB BS, MD or equivalent combination of education, training and relevant industry experience
Technical knowledge & skills or other requirements:
- Must demonstrate understanding of drug development clinical trials.
- International experience preferred.
- Device and/or combination product experience preferred.
- Highly organized with attention to detail
- Strong verbal and written communication skills are required, as well as excellent scientific writing, presentation and documentation skills.
- Working knowledge of electronic publishing/file management system
- Exceptional selfmanagement ability
- Travel as needed.
Work experience:
- Clinical experience preferably in Ophthalmology
- Medical device industry experience (desirable)
- Experience in a strategic leadership capacity
- Locations preferred
- APAC or UK or US
