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CRA I Jobs in Beijing, CHN - Covance

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CRA II, Shanghai
Covance  - Beijing, CHN
Clinical Research
Responsibilities/Duties - Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, with or without guidance; liaise with vendors; and other duties, as assigned - Responsible for aspects of registry management as prescribed in the project plans - General On-Site Moni ... Read More
CRA II, Beijing
Covance  - Beijing, CHN
Clinical Research
Responsibilities/Duties - Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, with or without guidance; liaise with vendors; and other duties, as assigned - Responsible for aspects of registry management as prescribed in the project plans - General On-Site Moni ... Read More
CRA II, Shanghai
Covance  - Beijing, CHN
Clinical Research
- Assures the implementation of project plans as assigned. - Site administration and site monitoring responsibility for clinical studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP. - Site management responsibility for clinical studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP. - Act in the project role of as Local Project Coordi ... Read More
CRA II, Beijing
Covance  - Beijing, CHN
Clinical Research
We are always looking for talented professionals with the clinical industry to join us as Clinical Research Associate in Beijing, China. If you are already working in the clinical trial industry with good understanding on clinical trial process and have experience on CRA, we want to talk to you about your career development. Covance is committed to providing a career with purpose in a culture th ... Read More
CRA II, Beijing
Covance  - Beijing, CHN
Clinical Research
Responsibilities/Duties - Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, with or without guidance; liaise with vendors; and other duties, as assigned - Responsible for aspects of registry management as prescribed in the project plans - General On-Site Moni ... Read More
CRA II
Covance  - Beijing, CHN
Clinical Research
Responsibilities/Duties - Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, with or without guidance; liaise with vendors; and other duties, as assigned - Responsible for aspects of registry management as prescribed in the project plans - General On-Site Moni ... Read More
SCRA, Taipei
Covance  - Beijing, CHN
Clinical Research
-Responsible for all aspects of study site visits and site management and monitoring activities ex. f/u SAE, clinical supply, etc -Prepare accurate and timely trip report -review progress of projects and initiate appropriate actions to achieve targets -feasibility work, site selection, EC submission, RA submission, translation of study documents, negotiate study budget, contract - Assist with tra ... Read More
Clin Res Assoc II
Covance  - Beijing, CHN
Clinical Research
- Assures the implementation of project plans as assigned - Site administration and site monitoring responsibility for clinical studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP - Site management responsibility for clinical studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP - Act in the project role of as Local Project Coordinat ... Read More

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