Job Responsibilities:
1. Fully responsible for the implementation and management of the company's projects, formulate product clinical development strategies and clinical plans, and promote the success of the company's product clinical trials; interpret relevant clinical research data, and participate in the formulation of the company's new technology and product transformation research strategies;
2. Organize the formulation of clinical research project budgets and implementation plans, be responsible for the full-process management of clinical trials, solve key problems in the advancement of clinical research projects, and ensure the smooth implementation of clinical research projects;
3. Responsible for the progress and quality of clinical research projects, conduct regular/stage evaluations, and report project progress to the company on a regular basis;
4. Responsible for the review/approval of relevant documents for clinical research project management: contracts, plans, plans, reports, etc.;
5. Provide medical training and support for project teams or researchers on project-related issues, including writing medical training materials for project research teams, and providing medical knowledge and project training in related treatment fields;
job requirements:
1. Under 40 years old, doctoral or post-doctoral bioengineering, pharmacy and other related majors;
2. Related work for more than 5 years;
3. Experience in research and development of inhaled drug delivery is preferred.
Salary and benefits:
The company provides market-competitive salary and benefits, project rewards, option plans, etc., and assists those who meet the high-level talent policies of Shenzhen and Zhuhai to apply for talent subsidies worth over one million yuan from the municipal government, as well as supporting subsidies from the district government. Shenzhen Peacock talents are welcome Submit your resume, welcome industry elites to join us, lead innovation, and create a better future!