First-level areas：Biotechnology
First-level areas：Bioinformatics Technology
Source：Social Recruitment
Job description ：
Job Responsibilities.
1. Responsible for initiating clinical trial projects in the medical department and conducting internal discussions;
2. Responsible for communicating with the sponsor, review department, clinical unit, and various departments of the company to determine the plan ideas, including but not limited to the clinical department, statistics department, quality control department, registration and pharmacy department, etc;
3. Responsible for reviewing project proposals, researcher manuals, informed consent forms, research medical records, CRF, PPT, and providing professional technical support;
4. Host coordination meetings and expert consultation meetings, provide proposals and related materials based on the opinions communicated by the project team, present PPT, listen to and confirm the opinions of the coordination meeting experts, and arrange revisions to the proposals and related materials accordingly;
5. Review and determine the opinions of the ethics committee, and properly arrange for the revision of ethical materials;
6. Provide leading opinions on technical issues raised by researchers and project managers (supervisors) during the project implementation process;
7. Participate in the formulation of statistical analysis plans, review statistical reports by the statistics department, guide the writing and revision of summary reports;
8. Responsible for communication and answering questions with CDE and related technical departments, guiding medical managers to complete formal Q&A or reply letters;
9. Host internal scheme discussions, external scheme consultation meetings, and professional meetings related to the project;
10. Accept company delegation to attend industry and related professional conferences and give keynote speeches.
Job requirements.
1. Doctorate or Master’s degree in Clinical Medicine;
2. At least 2 years of clinical professional experience and 3 years of CRO work experience;
3. Clinical specialties, including traditional Chinese medicine, Western medicine, and integrated Chinese and Western medicine, familiar with relevant regulations on clinical trials;
4. Proficient in drug clinical trial protocol design, participated in and led multiple clinical trial protocol designs for oncology or biopharmaceutical projects.

Please send your CV or resume as an attachment to the following email address:
mailto: rbhr@hrcenter.co.uk
With the subject line formatted as: ‘Name + Position + Company Name + Location’.