Job Description:

• Complete the program writing and summary report writing of the project in charge, largely independently.
• Independently complete the medical monitoring of the project and develop regular medical monitoring reports
• Answer medical questions for projects he/she is responsible for, largely independently
• Independently complete the review of relevant documents in other departments responsible for the project
• Able to communicate independently with other project team members
• Assist supervisor in completing business bidding activities, review literature, createPPTetc.

Job Description:

• Complete program writing and summary report writing for projects under the guidance of the superviso
• Complete medical monitoring of the projects and write medical monitoring reports regularly, under the guidance of superiors
• Communicate and interact with other project team members, under the guidance of supervisors

Job Description:

• Assist statisticians with the statistical analysis of clinical trials;
• Create the project files of adam, tlf, etc. with sas according to the sap and tlfshell written by the statistician and thecdiscstandard;
• Check data against checklist to ensure accurate data generation;
• Maintain smooth communication with team members and clients to ensure that projects are completed according to the statisticians' and clients' requirements;
• Ensure that all phases of the project are implemented in accordance with sop requirements.

Job Description:

• Review case report forms, guidelines for filling of case report forms, data verification plans, database design instructions, database updates, and other documents. 
• Develop random schemes and generate random codes. 
• Develop and review statistical analysis plans and TFL templates. 
• Generate and proofread analytical data sets and statistical analysis charts, review TFLs for consistency. 
• Develop and review statistical analysis reports. 
• Review clinical study reports.

Job Description:

• Write documents related to clinical trial data management (e.g. data management plan, etc.) and be responsible for maintaining, updating and archiving of such documents. 
• Responsible for the design of the medical case report form (CRF) and the validation of the EDC system and user acceptance testing (UAT).;
• Complete the entry, verification, checking and maintenance of CRF data and external electronic data;
• Verify data according to the data verification plan, issue data query forms for suspicious data, resolve data queries, and update the database.  
• Responsible for data review and consistency checks for serious adverse event prior to database lock. 
• Perform the entry of normal value ranges for laboratory data when necessary. 
• Perform data export and generating listing report listing for clinical statistical analysis；
• ConductCDM under the requirements of relevant laws, regulations and guidelines, and responsible for the quality control of the entire process;
• Complete consistency check reports and progress reports within the required time frame, responsible for medical coding and complete data query form as needed ； 
• Complete other related work of the department. 

Job Description:

• Customer development and follow-up visits

• Develop customers according to the company's assignments and independently complete customer development, follow-up and visits, including but not limited to, acquiring contact information, establishing communication channels, and conducting analysis on customer pipeline and potential value for new customers; conduct daily follow-up visits to customers with established contact channels and regular updates of all information.

• Improve relevant follow-up records and collect information according to the Specification for Daily Commercial Work, and update the data acquired in CRM in a timely manner;

• Conduct regular (monthly/quarterly/yearly）analysis of follow-up clients; timely optimize the list of follow-up clients;Conduct regular follow-up visits to cooperated customers to obtain customer satisfaction information, timely feedback it to the company, and cooperate with the company to deal with related customer satisfaction issues.

• Sales opportunity follow-up

• Work on the whole process of sales opportunity follow-up independently.

• Conduct feasibility analysis of acquired sales opportunities and report to the company on the decision of whether to follow up.

• Develop plans for sales opportunity follow-up

• Coordinate and organize internal and external resources of the company to complete the organization planning and implementation of bidding activities, if need.

• Organize the company's external resources to completing the plans for sales opportunities as the responsible person, and organize all departments to analyze the offer parameters and finalize the offer.

• Regularly analyze acquired sales opportunities and optimize the list of follow-up sales opportunities in a timely manner; regularly analyze, summarize, and report on sales opportunities to assist the company in achieving established sales targets.

• Conduct business negotiations for intentional sales opportunities, be responsible for drafting and signing of business contract, as well as payment collection.

• Reach agreements in sales opportunities, organize internal handover arrangements and complete written handover forms.

• Regularly follow up on contracts converted from sales opportunities, to collect, summarize and report on customer satisfaction information, and to assist the company in dealing with customer satisfaction issues."

Job Description:

• Conduct quality control activities according to the quality control plan, develop quality control reports and suggested corrections for problems found, review CAPAplans, and follow up CAPAuntil closure
• Assist HRdepartment with training sessions
• AssistQCM QCM in internal issue sorting and report analysis, follow up on CAPAissues, and complete the closed loop ofCAPA
• Complete other matters as assigned byQCM

Job Description:

• Manage and coordinate the work of the project team, including relevant functional departments and suppliers, to ensure that the project is completed on schedule.
• Organize project team members to complete clinical study documentation, including but not limited to protocols, investigator manuals, informed consent documents, project plans, budgets, etc.
• Create and maintain trial master file (TMF)and perform quality control to ensure documentation integrity.
• Develop project management plans, schedules and progress reports to guide and understand project conditions.
• Coordinate and ensure effective cooperation between departments, maintain communication with all members of the study team, and direct the daily work of the study team members to ensure that all work is carried out properly.
• Ensure communication and reporting with the sponsor as scheduled, develop solutions to correct deviations from the budget
• Lead the team to solve problems such as risk management, emergency management, etc., to ensure that the project is carried out as planned, and both the project quality and progress meet the requirements;
• Establish and maintain good relationships with sponsors, study institutions to ensure continuous improvement during the project implementation process.
• Participate in the management and training of the department, participate in bid development and bidding, and perform other duties as assigned by the management layer.

Job Description

• Conduct research screening, monitoring and closure visits of study centers in accordance with the trial protocol, scope of work as contracted, SOP and GCPrequirements.
• Conducting program and study-related training for the study centers he/she is responsible for and communicating with the study centers to meet requirements and solve issues during project implementation.
• Assesses the quality and integrity of the work of the study center to determine whether studies are being conducted in accordance with the protocol and applicable regulations; reports quality issues to the responsible clinical project manager and clinical line manager and take responsive measures actively.
• Manage the progress of the study, the generation and resolution of data queries in the center he/she is responsible for; monitor visits and related documents of action plans, submit visit reports and other required documents.
• Responsible for the financial management of the study center and other tasks assigned by the line manager.
   

Job Description

• Responsible for the organization and preparation of clinical department meetings and the writing of meeting minutes.
• Responsible for reimbursement applications and invoice tracking of clinical department projects
• Responsible for administrative tasks related to the clinical department and to provide support to team members in the implementation of clinical trials.
• Assist the clinical study team in the preparation, processing, distribution, filing and archiving of clinical study documents and reports as needed, according to the scope of work and SOPs. Assist with regular checks on the accuracy and completeness of study documents. 
• Assist the project manager in the preparation, handling and distribution of clinical trial materials as needed and keep tracking data.

Job Description

• Responsible for the organization and preparation of clinical department meetings and the writing of meeting minutes.
• Responsible for reimbursement applications and invoice tracking of clinical department projects
• Responsible for administrative tasks related to the clinical department and to provide support to team members in the implementation of clinical trials.
• Assist the clinical study team in the preparation, processing, distribution, filing and archiving of clinical study documents and reports as needed, according to the scope of work and SOPs. Assist with regular checks on the accuracy and completeness of study documents. 
• Assist the project manager in the preparation, handling and distribution of clinical trial materials as needed and keep tracking data.