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
Clinical Data Analyst
Responsibilities Include:
- Provide input from the data management perspective regarding the design of clinical trial protocols.
- Design and develop case report forms (CRFs)...(more)
Clinical Project Manager
Responsibilities
The qualified candidate will be an experienced Clinical Project Manager that is capable of handling...(more)
Clinical Data Manager
The candidate is responsible for providing timely and
professional ongoing quality management of clinical
trial data by identifying errors/inconsistencies in
CRF data and...(more)
Clinical Data Manager
As part of a clinical working group, the Sr. Clinical Data Manager (CDM) is responsible for the accuracy and completeness of the clinical data collected during a clinical...(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)
Clinical Project Manager
Title: Clinical Trials Project Manager
General Summary:
The Clinical Trials Project Manager will report to and work closely with the Project Director in the coordination and management of...(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)
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 Research Associate (CRA)
Title: Clinical Research Associate
Country United States
Description
- Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (40 - 50% travel) for GCP...(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)