Spotlight Employers
Clinical Research Coordinators
Clinical Research Coordinators (CRC) monitors clinical trials while working in a team environment under the direction of Clinical Research Associates and Principle Investigators. The responsibilities of a CRC include arranging for a research study site; recruiting, screening and enrolling clinical study participants; arranging follow-up visits; maintaining and dispensing drug and other study supplies; completing and ensuring the accuracy of case report forms and regulatory documents; and ensuring the adherence to good Clinical Practice guidelines.
Employment Outlook
Career opportunities for Clinical Research Coordinators are commonly found in hospitals, physicians’ offices, contract research organizations, biomedical research organizations and institutions, specialty disease centers and pharmaceutical and medical device suppliers. With the growth of the Biotechnology industry, CRC positions are expected to increase 20% or more in the next 10 years. Clinical Research Coordinators earn an average of $14.74 to $29.88 an hour for an annual salary of $30,659 to $62,150 a year or higher, depending on degrees obtained, the research setting, credentials and experience.
Current Job Openings
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MD (physician) - Medical Affairs / Safety Specialist
Description -
-medical monitoring
-Pharmacoviglance
-Writing safety standards
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Clinical Data Manager
Sanofi Pasteur in the USA is a leader in the research, development, manufacture, marketing and sales of vaccines and immunological products because here we clearly see a better tomorrow for all...(more)
Clinical Research Associate (CRA)
Description
i3 Research is a full-service contract research organization (CRO) focused on four CORE areas: central...(more)
Clinical Research Manager
Fast growing clinical research organization seeks clinical research manager with at least 4 years of oncology study management experience.
Description -
- Manage interdisciplinary clinical...(more)
Clinical Research Associate (CRA)
Responsibilities
Responsibilities primarily involve management of assigned investigational study sites including: prestudy, initiation, monitoring and study close-out site visits....(more)
Clinical Data Programmer
Successful candidate will work as part of a project team, or possibly as a team manager, to design and implement applications in support of clinical research and biostatistics. Candidate will...(more)
Medical Writer
Job Summary
The medical writer in Regulatory Services is responsible for assisting the Senior medical writer in managing the effective and efficient utilization of...(more)
Drug Safety Associate
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Clinical Project Manager
CLINICAL DATA MANAGER
COMPANY INFO:
MedFocus offers clinical research contract outsourcing and staffing specifically to the pharmaceutical, biotechnology and medical device...(more)
Clinical Data Manager
:
Under general supervision, the Clinical Data Manager reviews data; assists in database design and testing; designs CRFs and guidelines; designs and tests logic checks;...(more)