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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Real Life Sciences South San Francisco, CA
The Clinical Research Associate (CRA) will be responsible for initiation, monitoring and other tasks associated with clinical studies. The CRA will be responsible for investigational site management for clinical studies, and will assist in the creation and implementation of protocols, informed consents, case report forms, clinical study reports and related study materials. He/she will also provide...
Description: - Works under general supervision, and participates in the design, planning, implementation and overall direction of clinical research projects. - May co-ordinate the activities of relevant colleagues within the Company and investigators to ensure compliance with the overall scientific study objectives. - May work with international investigators and key customers as well. - Recei...
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...
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...
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...
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 ...
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 Guidelines...
OV Clinical Trials Paterson, NJ, 07505
OV Clinical Trials is looking for an RN for Clinical Research Contract work – part-time and short term. This position will visit sites to support the site staff in identifying patients who are eligible for clinical research studies. Nurse will be responsible for completing a report summarizing the findings from chart review. Co-ordinate and reach out to other clinics , gastroenterologists / hepa...
Yoh Wilmington 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 loc...
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...
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 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...
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...
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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