广州招聘

Overall Job Purpose:
The Clinical Trial Assistant (CTA) has the responsibility for the successful delivery of the assigned clinical research tasks within his/her defined territory under the supervision of the (A)CRM/(A)CRD.

1. Key Accountabilities
1.1 Project Related Accountabilities
· Provide general administrative support to the clinical study team and assistance
to Project Managers (PMs).
· Assist the clinical study team in completion of all required tasks to meet
departmental and project goals.
· Support the clinical study team with ongoing conduct of studies.
· Be familiar with ICH-GCP, appropriate regulations, relevant SOPs and internal
tracking systems.
· Be familiar with the roles and responsibilities of the CRA including site
visits, if appropriate.
· Assist project teams with study-specific documentation and guidelines as
appropriate.
· Set up, organize and maintain clinical study documentation (e.g., Trial Master
Files, CRFs, etc.) including preparation for internal/external audits, final
reconciliation and archival.
· Process Data Collection Forms, i.e., logging in, tracking and quality
controlling as appropriate for the study.
· Coordinate ordering/dispatch and tracking of project materials (e.g., CRFs,
diary cards, lab supplies, IP supplies) as appropriate.
· Assist in the tracking and distribution of safety reports.
· Coordinate document translation, if required.
· Attend project team meetings and generate meeting minutes.
· Assist in the production of slides, overheads, etc., as needed for project,
departmental, sponsor and/or business development presentations.
· Other duties as assigned by PMs/CRMs/CRDs.
1.2 Relationship Management
· Be responsible for contributing to the establishment of a strong team spirit.


2. Job Requirements
2.1 Skills
· Good communications skills.
· Very good working knowledge of relevant software such as MS-office (Excel, Word
and PowerPoint, etc).
· Strong attention to details.
· Ability to successfully work in a team environment.
2.2 Education
· College degree or above, majoring in medical, pharmaceutical or bio-science.
2.3 Language Skills
· Good in written English as well as local language.
2.4 Minimum Work Experience
Previous CTA or assistant experience is preferred.

  Beijing Health Tech Medical Group (HT-Med) was founded since 2004. We are a comprehensive medical Operation and development organization .Assemble excellent talents of medicine, pharmacy, data management and statistical fields, offering professional services to support biotech and pharmaceutical companies at every stage of product lifecycle .
 
 We provide Medical translation, Data Management, Statistical Analysis, Medical Writing, Regulatory Affairs, Project Evaluation and Management, Independent Audit, Training, CRA/CRC/DM dispatch. Since we established, we were developing new drugs with Chinese Academy of Medical Sciences, Peking University Health Science Center, The General Hospital of the PLA, Military Medical Sciences, etc. Has cooperated with over 90% clinical trial sites (hospital) approved by SFDA.

  We developed independently EDC+CTMS by ourselves, obtained 3 patents and 2 brands. Basing on excellent IT capability, we develop Products Data Center for our clients, and created role exchange pattern between CRA and CRC, improved speed&quality of Clinical Study by the model of EDC+CRC, especially in PMS. We have been became the vendor of lots of global company (AZ, GSK, BI, Abbott, Roch, Mundipharma, QPS etc.) and some official Institution (Chinese Academy of Medical Sciences, Peking university, The general hospital of Chinese PLA, Sanming hospital, Zhejiang oncology hospital, Academy of Military Medical Sciences of the Chinese PLA etc.).

 We are familiar with China SFDA policy and CDE mentality, possessing mass of expert resource and marketing support. we could cover 90% Chinese certificated clinical research hospital by lots of home-based employee in 18 cities.

  公司网址：http://www.ht-med.com