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 Data Manager
Minimum Qualifications :
- Five years of experience OR the equivalent combination of education and experience with a...(more)
Clinical Research Coordinator (CRC)
General Summary of Duties
Provides professional nursing care and monitoring for research patients. Performs duties involved in...(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)
Biostatistician
Job Summary
Act as the lead or back-up statistician for Kendle projects with low to moderate complexity. May act as the supportive statistician for Kendle projects with...(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)
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)
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 Associate (CRA)
Exciting regional home-based permanent opportunity with one of the fastest growing International Clinical Research Organizations in the country. CRA's with 2-3 year of oncology monitoring...(more)
Drug Safety Associate
MD (physician) - Medical Affairs / Safety Specialist
Description -
-medical monitoring
-Pharmacoviglance
-Writing safety standards
-Writing narratives on...(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)