Spotlight Employers
Quality Assurance Specialists
The Quality Assurance Specialist ensures that all quality assurance-related activities surrounding a clinical trial are compliant with any and all regulatory requirements and standards. It is also the responsibility of the Quality Assurance Specialist to conduct regular audits of all clinical work and to review and analyze finding from trials.
To succeed in this role, qualified candidates must hold a four-year degree and be highly familiar and experienced with processes and procedures in the clinical environment.
Employment Outlook
Opportunities for Quality Assurance Specialists can be found in hospitals, contract research organizations, biomedical research organizations and institutions, sectors of the government, and specialty disease centers and pharmaceutical and medical device suppliers. Quality Assurance Specialist positions are expected to increase 10% or more in the next 10 years. Quality Assurance Specialists earn an average of $24.75 to $31.88 an hour for an annual salary of $51,500 to $66,300 a year or higher, depending on degrees obtained, the research setting, credentials and experience.
Current Job Openings
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)
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)
Clinical Project Manager
Responsibilities
CLINICAL PROJECT MANAGER
The successful candidate will be responsible for...(more)
Clinical Research Associate (CRA)
Clinical Research Associate
Description:
Assists in the design, planning, and implementation of clinical research projects. Coordinates activities between company, Contract...(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)
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 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 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 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)
:
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)