Clinical Research Co-Ordinator Jobs

Currently, there are no Clinical Research Co-Ordinator jobs available which match this search. You may wish to explore similar job titles on the Science jobs page or view related jobs below.
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Covance Costa Rica
• 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. • General On-Site Monitoring Responsibilities (a) Ensure the study staff who will conduct the protocol have received the proper materials and instructions to...
Duties: -Co-ordinate and manage logistics for different groups in Pleasanton, CA and Marlborough, MA as well as external sites which includes: logistics management of materials, samples, shipment schedules, etc. -Data management for the groups, and study sites, check for accuracy of forms and documentation from site personnel etc. Job Description: 1. After introduction to the process, assist i...
Covance Malaysia
• 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...
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 ...
Covance Israel, TX
Position : Clinical Research Associate (with phase II epilepsy and ideally between 2 to 5 years of monitoring experience) Division : Oursourcing Location : Israel - office-based or home-based 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, providi...
Covance Australia, Sydney
• 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 wh...
SUMMARY: Objectives of the Position To ensure timely implementation of clinical research plans for assigned products To ensure investigator and site compliance with the study protocol, FDA regulations, ICH Guidelines and Good Clinical Practice (GCP) To coordinate and execute clinical research activities for multisite clinical studies Clinical Research Associate 1. Works under general supervi...
CoSource/Covance is seeking Oncology Sr CRAs to work with us as a Functional Service Provider for a large pharmaceutical company. *ONCOLOGY is required* 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 Guideli...
CoSource/Covance is seeking Oncology Sr CRAs to work with us as a Functional Service Provider for a large pharmaceutical company. *ONCOLOGY is required* 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...
Clinical Study Manager needed for a contract opportunity with Yoh`s client located in Wilmington, DE. What You`ll Be Doing: - Overall responsibility for the study commitments within the country, for timely delivery of data to required quality as per SMA. - Lead Local Study Team(s) consisting of monitors and study administrator(s). - Lead and optimize the performance of the local Study Team(s) ...
Clinical Study Manager needed for a contract opportunity with Yoh's client located in Wilmington, DE.What You'll Be Doing:- Overall responsibility for the study commitments within the country, for timely delivery of data to required quality as per SMA.- Lead Local Study Team(s) consisting of monitors and study administrator(s).- Lead and optimize the performance of the local Study Team(s) at count...
Our client is currently seeking a Contract Study Manager III. - year long contract opportunity with a sponsor company in the Wayne, PA area. Requires strong study management / operations experience; Oncology or Hematology a plus. This job will have the following responsibilities: Leads/supports the clinical team(s) to deliverthe clinical development plan. Provides input to the development strate...
Working with the Global Safety Physician (GSP), take responsibility for aspects of the Clinical Safety strategy for assigned AstraZeneca-MedImmune drug projects and products throughout all stages of development and/or when on the market, including implementation and communication of the strategy at the project team/governance level. Identify opportunities for, or the need to, enhance existing pro...
The Director, Vector Production will oversee activities related to the Process Development and in-house non-GMP/cGMP production of recombinant Adeno-associated Viral Vectors (rAAV), and cGMP vector production at contract manufacturing organizations (CMOs). ESSENTIAL FUNCTIONS: 1.Manage the Process Development, GMP production, testing and fill finish of rAAV products at CMO's 2.Manage internal a...
Quintiles pioneered the idea of helping pharma companies conduct objective clinical trials to establish not only whether a drug is effective, but who can take it safely. Our customers have relied on us to design and conduct rigorous clinical research for decades, from small studies to multinational mega-trials. However, we continue to develop new ways of interpreting and evaluating data that allow...
Quintiles pioneered the idea of helping pharma companies conduct objective clinical trials to establish not only whether a drug is effective, but who can take it safely. Our customers have relied on us to design and conduct rigorous clinical research for decades, from small studies to multinational mega-trials. However, we continue to develop new ways of interpreting and evaluating data that allow...
Quintiles pioneered the idea of helping pharma companies conduct objective clinical trials to establish not only whether a drug is effective, but who can take it safely. Our customers have relied on us to design and conduct rigorous clinical research for decades, from small studies to multinational mega-trials. However, we continue to develop new ways of interpreting and evaluating data that allow...
Quintiles Inc. San Diego, CA, 92140
Quintiles pioneered the idea of helping pharma companies conduct objective clinical trials to establish not only whether a drug is effective, but who can take it safely. Our customers have relied on us to design and conduct rigorous clinical research for decades, from small studies to multinational mega-trials. However, we continue to develop new ways of interpreting and evaluating data that allow...
Quintiles Inc. Atlanta, GA, 30301
Quintiles pioneered the idea of helping pharma companies conduct objective clinical trials to establish not only whether a drug is effective, but who can take it safely. Our customers have relied on us to design and conduct rigorous clinical research for decades, from small studies to multinational mega-trials. However, we continue to develop new ways of interpreting and evaluating data that allow...
Description Quintiles pioneered the idea of helping pharma companies conduct objective clinical trials to establish not only whether a drug is effective, but who can take it safely. Our customers have relied on us to design and conduct rigorous clinical research for decades, from small studies to multinational mega-trials. However, we continue to develop new ways of interpreting and evaluating da...

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