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 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 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 Coordinators (CRCs) working in a team environment under the direction of the Director of Operations and Investigators assisting in the health and welfare of study...(more)
Clinical Research Associate (CRA)
- Conducts site monitoring of clinical research studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP.
- Provide clinical...(more)
Biostatistician
Position Title: Biostatistician II
Working Location: Durham, North Carolina
Employment Status: Full-Time Regular
Required Experience: 2 years
Required Education: Masters...(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)
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)
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
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 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)