Ophthalmic clinical job responsibilities

Ophthalmic clinical job responsibilities

In the era of continuous progress, more and more people will be exposed to job responsibilities. Job responsibilities refer to the work content that a post needs to complete and the scope of responsibility that it should undertake. The post is the unity of duties and responsibilities, which consists of two parts: the scope of authorization and the corresponding responsibilities. So do you really know how to formulate job responsibilities? The following are my clinical duties in ophthalmology. Welcome to read the collection.

Regular job responsibilities:

1. Formulate departmental SOP, management system and workflow, and organize their implementation;

2. Fully responsible for clinical research projects (including project implementation, quality, time, cost and researcher satisfaction);

3. Grasp the progress in this field, actively explore available resources, speed up the project progress, and ensure that the project quality meets the requirements of new drug registration;

4. Be familiar with the clinical project plan and related implementation requirements, and train and guide the project team;

5. Ensure the reasonable application of the project budget;

6. Actively interact with the main researchers in each center to increase the satisfaction of researchers;

7. Guide the start-up and opening-up of each project team, track the progress and quality of the project, and ensure that the clinical trial projects in charge comply with GCP and relevant national laws and regulations;

8. Check and evaluate regularly to ensure the completeness, accuracy and compliance of the research data of each project team (in line with various laws and regulations on medical research and the company's procedures), and report it at the regular meeting of the department;

9. Responsible for the cooperation of all audit departments and project teams, including sharing successful experiences, summing up lessons from failures, determining the implementation of the company's existing procedures, and establishing and perfecting necessary procedures.

10. Responsible for coordinating the communication between each project team and other departments;

1 1. Be responsible for the performance appraisal of department members and the inspection and improvement of nonconformities, and formulate preventive measures for nonconformities;

12. discover and cultivate internal talents and participate in recruiting external talents;

13. Organize and be responsible for training and setting up the project team;

14. Strive to be a leader in this field.

Requirements:

1. Bachelor degree or above in medicine, pharmacy or related major.

2. More than five years management experience in related industries, and engaged in more than one immunization or ophthalmology project audit.

3. Received systematic project management and GCP related knowledge training;

4. Work with careful planning, overall concept and good communication skills;

5. Good health, self-discipline, initiative, ability to work under pressure and courage to take responsibility;

6. Familiar with the operation mode and workflow of clinical trial industry, and familiar with the laws and regulations of GCP related industries.

7. Have the ability to judge, analyze and make decisions independently;

8. Have good organization and coordination skills and expression skills;

9. Have the professional concept of project execution network control system and complete and mature management experience;

10. Have good evaluation ability and be able to give guidance or guidance to subordinates' work;

1 1. Strong learning and innovation ability.

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