To be responsible for providing project co-ordination and operational solutions
To support Country Study Managers (CSMs) and to provide clinical trial oversight to local study teams to enable effective management of both global and local trials
To be a subject matter expert on all Study Start-up (SSU) related activities in Hong Kong, oversees and leads SSU activities in collaboration with other clinical research stakeholders and serves as a leader for Hong Kong process improvements and patient recruitment strategies.
You’re someone who wants to influence your own development. You’re looking for a company where you have the opportunity to pursue your interests across functions and geographies. Where a job title is not considered the final definition of who you are, but the starting point.
Preferably, you should be/have:
At least 1 years of experience as a Clinical Research Officer
In-depth knowledge of ICH-GCP clinical trials related requirements
Clinical project management skills
Experience working as part of a team with a proven ability to make an active contribution to the team’s performance and teamwork
Able to prioritize and manage multiple tasks with high flexibility
Proven project management skills to work with variety of different systems and stakeholders and deliver commitments on time and with quality
Self-motivated and displays initiative/resourcefulness
Ability to work independently with limited supervision
Strong attention to detail
Demonstrated computer literacy, usage of MS Office software, web-based systems and databases
Ability to communicate clearly and accurately in both written and spoken English and Chinese
Excellent communication skills, good interpersonal skills and analytical skills
At Roche, 94,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity.