Develop the company's medical strategy from a strategic perspective.
Establish a clinical quality system that complies with regulations and guide the writing and revision of clinical research documents.
Select clinical research partner institutions, oversee the organization, implementation, supervision, and evaluation of clinical trial research and other clinical projects.
Participate in product registration's clinical evaluation to assess effectiveness, safety, adverse events, and their impact.
Collaborate with product management and development teams to drive product exploration based on clinical needs and current situation.
Establish and maintain academic and industrial KOL resources in the field of clinical medicine.
Fulfill other tasks assigned by superiors.
Job Requirements
Hold a master's degree or above in clinical medicine, pharmacy or biomedical engineering.
Possess over 10 years of experience in conducting clinical trials for Class III medical device companies or CROs along with more than 5 years of project/team management experience.
Demonstrate successful experience in launching new products as well as forward-thinking mindset regarding medical affairs layout strategies.
Exhibit familiarity with regulations related to clinical quality standards, complete process of medical device R&D including clinical trials; also knowledgeable about domestic and international developments in the field of clinical research.
Display excellent communication skills along with strong abilities in coordination, resource integration, team management; possess leadership qualities as well as problem-solving skills including emergency plan management capabilities.
