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Clinical Research Jobs

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Search results: 1 - 10 of 135

CRA II, Beijing (48051BR)

COVANCE. Beijing

- 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...

COUNTRY China
INDUSTRY Clinical Research

Project Manager, 临床项目经理 (47686BR)

COVANCE. Shanghai

- Serve as Project Manager for domestic and/or international (typically intercontinental) projects for one or more clients, according to Covance Standard Operating Procedures, ICH Guidelines and GCP . - Responsible for total study revenues of up to 5M annually. - Responsible for the successful conduct of assigned projects. - Serve...

COUNTRY China
INDUSTRY Clinical Research

Clinical Trial Manager (47902BR)

COVANCE. Beijing

A.Individual Contributor B.Job Duties: Commercial Responsibilities - Contribute to the operational plan and participate in the delivery of Bid Defense presentations for new business, as required. - Develop and maintain relationships with assigned clients and serve as the client interface for all clinical operations matters. Meet/exceed client satisfaction expectations. Initiation...

COUNTRY China
INDUSTRY Clinical Research

Global Site Services Specialist, Beijing (47688BR)

COVANCE. Beijing

We are looking for talented clinical research professionals for Global Site Services Specialist 临床试验启动专员 in Beijing. If you are an expert in site start up area, we would love to speak to you on our Global Site Services Specialist 临床试验启动专员 opportunity. Covance is committed to providing a clinical research career...

COUNTRY China
INDUSTRY Clinical Research

Data Entry Associate (47649BR)

COVANCE. Leeds

Covance CRU is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. We are recruiting for our Clinic team in Leeds and are currently seeking to hire a Date Entry Associate on an initial 12 month fixed term contract to help support...

COUNTRY United Kingdom
INDUSTRY Clinical Research

Senior Clinical Research Associate (48143BR)

COVANCE. Madrid

Position : Senior Clinical Research Associate Location : Madrid - client-based Division : Outsourcing You can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Covance is one of the world's most dynamic drug development services companies, providing integrated, tailored solutions to the...

COUNTRY Spain
INDUSTRY Clinical Research

Clinical Research Associate (48144BR)

COVANCE. Madrid

Positions : Clinical Research Associate (2 to 4 yrs experience) Location : Madrid office-based Covance is one of the world's most dynamic drug development services companies, providing integrated, tailored solutions to the pharmaceutical and biotechnological industries. This is your chance to become part of a team that helps to bring...

COUNTRY Spain
INDUSTRY Clinical Research

SSU Specialist II, Hong Kong (47991BR)

COVANCE. Regional

- Develop project specific plans for the GSS component of assigned studies, liaise with operational project team regarding project issues (i.e., participate in team meetings) - Collect, review, approve process and track regulatory & investigator documents required for study site activation in accordance with Covance SOPs, sponsor SOPs, GCP ICH...

COUNTRY Hong Kong
INDUSTRY Clinical Research

CRA I, Shanghai (47641BR)

COVANCE. Beijing

- 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...

COUNTRY China
INDUSTRY Clinical Research

CRA II, Shanghai (47645BR)

COVANCE. Beijing

- 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...

COUNTRY China
INDUSTRY Clinical Research
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