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
Description
The primary focus of this position will be to perform a variety of complex and responsible tasks to enter,...(more)
Biostatistician
SENIOR BIOSTATISTICIAN
North Wales, PA
Exempt Position
...(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)
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)
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 Research Associate (CRA)
:
CLINICAL RESEARCH ASSOCIATE II
This is a lead position. The Clinical Research Associate II manages the implementation of study protocols at research sites. Responsibilities...(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 Research Coordinator (CRC)
General Summary of Duties
Provides professional nursing care and monitoring for research patients. Performs duties involved in...(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)
Clinical Research Associate (CRA)
The Clinical Research Associate II performs and coordinates all aspects of the clinical monitoring process in accordance with GCPs and global SOPs to assess the safety and efficacy of...(more)