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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
Regulatory Affairs Associate
Job Summary
The Associate Director Clinical Regulatory, is responsible for the effective and efficient utilization of regulatory personnel and resources related to the...(more)
Clinical Research Coordinator (CRC)
Fast growing physicins group seeking seasoned CRC for location 90 miles northeast of Raleigh, NC. Group conducts research across wide variety of therapeutic arenas.
Job Responsibilities...(more)
Clinical Financial Analyst
Under general direction, responsible for the production of timely and accurate financial reports for internal and external reporting purposes. Assist in preparation of work papers for the...(more)
Clinical Project Manager
Responsibilities
The qualified candidate will be an experienced Clinical Project Manager that is capable of handling...(more)
Clinical Research Associate (CRA)
Clinical Research Associate
Description:
Assists in the design, planning, and implementation of clinical research projects. Coordinates activities between company, Contract...(more)
Clinical Data Manager
Job Summary
Serves as the primary Kendle CDM contact with Sponsors and represents CDM on project teams. Responsible for project timelines, deliverables, financial...(more)
Clinical Research Associate (CRA)
This position performs and coordinates all aspects of the clinical monitoring process in accordance with GCPs and global SOPs to assess the safety and efficacy of investigational products...(more)
Clinical Research Coordinator (CRC)
General Summary of Duties
Provides professional nursing care and monitoring for research patients. Performs duties involved in...(more)
Drug Safety Associate
- Assist with the overall Clinical Safety and/or Pharmacovigilance operations associated with products including the entire adverse events process: which may include...(more)
Biostatistician
The Biostatistician Acts as lead statistician on projects of moderate to large size and complexity; support lead statistician on very large, complex studies. May have staff management and/or...(more)