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Responsibility
1.Responsible for delivery of assigned clinical programs, through effective partnership with the clinical partners, to enable optimized engagement leading to delivery of clinical project commitments (delivery on time, within budget and in compliance with regulations and SOPs).
2. Support clinical scientific discussions with regulatory agencies / notified bodies to drive support of the clinical and regulatory strategy, including proposed clinical investigations.
3. Follow SOP, GCP and other requirements to ensure the correct implementation of clinical trials, and provide training and guidance to team members.
4. To be responsible for the organization and coordination of the business within the department of medical affairs.
5. Participate in the project bidding of clients, establish good communication and cooperation with clients, and provide professional consulting services for clients.
6. Responsible for assigned tasks of drafting or/and updating SOP of medical affairs department.
7. Responsible for other tasks assigned by department’s leader and company leader’s team.
Qualifications
1. Master degree or above in life science, or bachelor degree and more than three
years working experience.
2. Clinical experience in oncology or chronic disease therapeutic area preferred.
3. Excellent ability of communication and execution, team spirit.
4. Languages: Excellent written and read English. Excellent oral English preferred.