Spotlight Employers
Clinical Research Monitors
The Clinical Research Monitor assumes an active role in all clinical research activities and is responsible for the timely and accurate monitoring of all patient data and study-related information from source documents and research records. Additionally, the Clinical Research Monitor assists in maintaining regulatory files in order to fulfill clinical research requirements and works closely with other clinicians as part of a collaborative team to ensure that all research is accurately completed and documented in a timely manner.
Because the Clinical Research Monitor is involved in all aspects of clinical research, an understanding of and solid experience in clinical research is required in addition to a four-year degree. Additional experience and knowledge may be necessary as dependent upon the nature of the setting in which the Clinical Research Monitor will be employed.
Employment Outlook
Career opportunities for Clinical Research Monitors typically exist in hospitals, physicians’ offices, contract research organizations, biomedical research organizations and institutions, specialty disease centers and pharmaceutical and medical device suppliers. Clinical Research Monitor positions are expected to increase 20% or more in the next 10 years.
Current Job Openings
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 Coordinator (CRC)
Clinical Research Coordinator
Aerotek Scientific has an immediate need for an on site Clinical Research Coordinator.
This candidate will expedite the trial...(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 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
ACRS is a fast growing Contract Research Organization located in Bannockburn, Illinois.
Job description: Clinical Data Managers (CDMs) are responsible for the quality and...(more)
Clinical Research Associate (CRA)
Senior Clinical Data Associate
Our client, a successful biotech organization based in Exton, PA is seeking a Sr. Data Manager to join their team. Our client offers a friendly and...(more)
Clinical Research Associate (CRA)
Seeking Experienced Regional Clinical Research Associates with in-depth experience!
-Conduct monitoring of multiple study sites. minimum of 4 years field monitoring
-Assess sites to...(more)
Clinical Data Coder
Job Summary
Serves as a resource primarily for the local Kendle Clinical Data Management (CDM) organization regarding the coding of clinical trials data (i.e. adverse...(more)
Clinical Research Associate (CRA)
We are a growing EastBay biopharmaceutical company focusing on Oncology drugs. We are currently seeking a Sr. Clinical Research Associate / Sr. CRA to oversee and manage our Phase 1-3...(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)