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Study Coordinator Jobs - Covance

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Study Coordinator II
Covance  - Greenfield, IN
Administration
Covance is currently seeking a Study Coordinator II for the Greenfield, IN site. As a Study Coordinator you will: - Provide study coordination support necessary for the performance of a wide variety of studies carried out in the BioCMC Large Molecule. - Oversee and participate in a wide range of co-ordination procedures, working with minimal supervision. - Will work closely with Lead Scientis ... Read More
Study Coordinator I
Covance  - Harrogate, UK
Biotechnology Pharmaceutical
Covance is one of the world's most dynamic drug development services companies, providing integrated, tailored solutions to the pharmaceutical and biotechnological industries. Duties include - Drafts protocols using study outline or client supplied information Prepares study protocol amendments Assists Study Director(SD)/Principal Investigator (PI) in study costing requests Prepares study sc ... Read More
Study Coordinator II
Covance  - Madison, WI
Administration
Covance is currently seeking a Study Coordinator II for the BioAnalytical Chemistry Lab Operations department at the Madison WI site. As a Study Coordinator you will: - Independently draft protocols, sample analysis outlines (SAOs), amendments and study schedules with some oversight, using proposal outline or client-supplied information. - Responsible for report preparation, including table an ... Read More
Study Coordinator II
Covance  - Chantilly, VA
Other
Study Coordinator Covance - Chantilly, VA Covance is currently seeking a Study Coordinator to join the team in Chantilly, VA> As a Study Coordinator you will:  Draft protocols, sample analysis outlines (SAOs), amendments and study schedules as appropriate, using proposal outline or client-supplied information.  Review study compliance against protocol, SOP, and regulatory agency guidelines.  ... Read More
Study Coordinator
Covance  - Harrogate, UK
Clinical Research
Covance is one of the world's most dynamic drug development services companies, providing integrated, tailored solutions to the pharmaceutical and biotechnological industries. Study co-ordinators are responsible for co-ordinating the administrative activities required in support of the conduct of studies within Immunochemistry. The key element of this post is to ensure that studies are administe ... Read More
Clinical Research Associate II
Covance  - Regional, NZL
Clinical Research
- 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; liaise with vendors; and other duties, as assigned - Responsible for all aspects of site management as prescribed in the project plans - General On-Site Monitoring Responsibilities o Ensure the study staff w ... Read More
Clinical Research Associate II
Covance  - Regional, NZL
Clinical Research
- 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; liaise with vendors; and other duties, as assigned - Responsible for all aspects of site management as prescribed in the project plans - General On-Site Monitoring Responsibilities o Ensure the study staff w ... Read More
Sr. Clinical Research Associate
Covance  - Regional, PR
Clinical Research
Job 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; liaise with vendors; and other duties, as assigned - Responsible for all aspects of site management as prescribed in the project plans - General On-Site Monitoring Responsibilities: o Ensure the ... Read More
Desktop Publisher
Covance  - Indianapolis, IN
Biotechnology Pharmaceutical
Covance is hiring a THIRD SHIFT Desktop Publisher for our Indianapolis, IN location. This position will begin as a 1st shift position and transition to third shift following the 3 month training period. The Desktop Publisher creates and modifies training manuals, requisitions and other relevant materials according to SOW requirements, providing on-time, quality project related documents. The Des ... Read More
CRA 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 Coordi ... Read More
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