Clinical Research Associate (CRA)

Job Description:

  1. Performs project supervision according to the plan and SOP, including early ethical communication, center start-up, routine supervision and center closure, and keeps all test and supervision records;
  2. Conducts supervisions and visits according to the requirements of the supervision plan and prepares inspection reports based on the inspection findings and work conditions;
  3. Maintains effective communication and collaboration between researchers and partners;
  4. Assists the clinical manager or team members in advance work preparation for specific tasks;
  5. Carries out other work related to clinical trials.

Job Requirements:

  1. Holds a Bachelor’s degree or higher granted by full-time unified enrollment universities, and has over 3 years’ work experience;
  2. Has good writing skills, able to guide the creation of copywriting and present the highlights of news publicity;
  3. Has divergent innovative thinking, independent thinking, a strong insight, and a good awareness of corporate image;
  4. Adept in the use of office software like word, excel and ppt;
  5. Has good learning ability, strong execution and communication skills;
  6. Has a work motivation, a strong sense of responsibility and a team spirit.

Preferred Abilities

  1. Experience in clinical trials of cardiac surgery instruments preferred;
  2. Experience in registration and ability to assist in registration material compilation preferred.
苏公网安备 32050502000890号 苏ICP备17050215号-1