Clinical Research Director

Additional Information

  • Post Title: Clinical Research Director
  • category: Health, Medical & Pharma
  • subcategory: Research jobs
  • No. of Vacancies: 1
  • Location: Beijing
  • Posting duration: 2009-4-15 ~ 2009-4-15
  • Level of Spoken Chinese: Fluent
  • Nationality: all
  • Education: bachelor
  • Work Experience: One Year
  • Gender: F/M
  • Age:
  • Work Status: Fulltime
  • Salary: negotiate
  • Position responsibilities and other requirements:
Duties and Responsibilities:
1、To provide constructive and valuable suggestions to clinical research development strategies.
2、Providing input to team to optimize contribution of clinical trial participation to global development strategies .
3、Be responsible for the organizational structure of building and determination of the position duties.
4、Manage staff in accordance with organization's policies and applicable regulations. Responsibilities include planning, assigning, and directing work; appraising performance and guiding professional development.
5、Be responsible for the organization and implementation of all clinical trails throughout the country.
6、To allocate the resources reasonably and control the progress of the clinical trials in order to finish the project within the fixed time and budgets. 
7、Clinical Quality Assurance. This includes the documentation of data collection methods and the development of SOPs related to the clinical trials division.
8、To maintain a good relations with the experimental units.
9、Any other responsibilities and duties which may be required from time to time.


Qualifications:
Minimum Education
Master's degree or above of Medical Science
Experiences
1、Rich working experience in conducting clinical trials, at least 5 years experiences in clinical research field including 2-3 years international/global studies experiences. 
2、Overseas work experience.
3、Good project achievements to be proved in previous working experiences.

Skills/Knowledge
1. Knowledge of medical terminology and clinical patient management;
2. Knowledge of ICH -GCP and local regulations regarding clinical studies and the conduct of such studies; 
3. Excellent organizational, communication, and interpersonal skills and ability to work within a matrix team environment required; 
4. Ability to establish and maintain effective working relationships with co-workers and clients; 
5. Ability to travel as and when required; 
6. Fluency English on both written & verbal.

  

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