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
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)
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)
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)
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
Responsibilities
CLINICAL PROJECT MANAGER
The successful candidate will be responsible for...(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 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)
- Conducts site monitoring of clinical research studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP.
- Provide clinical...(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
:
BIOSTATISTICAL ANALYST
Under general supervision the Biostatistical Analyst analyzes and interprets confidential data from a variety of sources. The Analyst is capable of...(more)
