Key areas respoibility:

Take on respoibility of leading clinical data from site site to achieve deliverables within agreed timelines and in accordance with scientific,qualityand/or regulatory requirements

Serve as the point peon between the hospitals and the clinical team

Support the design of data collection tools and relevant managerment forms

Work with the scientific data management team to test and implement improvements to the date reporting system

Assist in the review of raw data or patient profiles through data listing and resolve queries

Be respoible for medical and scientific content of clinical documents directed toward hospital audience

Present medical and scientific content to custome via phone,in peon or on line

Qualificatio(minimum requirements):

High degree of trust-confidence

Strong leadehip and excellent team player

Strong stewardship skills,excellent interpeonal skills and negotiation skills

Excellent communication shills(written and verbal)in local language

Excellent undetanding of the clinical development process,relevant diseases and therapies and the medical practice

Education:

Bachelor's degree or above of medical or pharmaceutical science

Professional experience:

NO

Supplementary job description:

Deqree of independent decisio:

Ability to work independently to make decision and problem solving

Level of independence,innovation and initiative:

Independence,innovation and initiative should always be demotrated when analysing,prionitising,planning and performing tasks either assigned by management or initiated by one self

Main stakeholdereputation and results:

Internai:team membe from clinical,scientific,sales and R&D functional groups

External:all the healthcare professionals,docto,KOL,vender respoible peon,CRO

CommunicatioInterication with othe internally or externally:

Serve as a focal point communication between the clinical team and various functio,Communicate to docto

update projrct progress and potential critical issues and report to management level