天津招聘

Main Accountabilities:

1.Prepare a clinical trial plan including all elements listed in the clinical trial plan template as appropriate for the clinical trial (Time Schedule, Budget, Recruitment Plan, Roles and Responsibilities, Work Breakdown Structure, Management Service Provider, Communication Plan, Risk Management Plan, etc).

2.Assist Clinical Science Manager or Clinical Research Physician design and preparation protocal in assigned.

3.To be responsible for clinical study sites selection and to ensure these sites are meet the Ferring's requirement and qualified with SFDA.

4.To be responsible for arranging and preparing of Advisory Board Meeting and Investigator Meeting.

5.To be responsible for the co-ordination of timely trial supplies with IMP department.

6.Responsible for the design and implementation of the CRF/e-CRF according to the final protocol in co-operation with the data manager.

Qualifications:

1.Bachelor's degree or above in Medical, Pharmacy or related areas.

2.Fluent English (oral and written).
3.At least 4 years experience in clinical trial execution and 2 years in global phrama or global CROs.

4.Work experience in Gynaecology-Obstetrics and/or Assisted Reproductive Technology area is preferred.