Spotlight Employers
Medical Writers
There are so many important responsibilities and personnel involved in clinical trials, and the resulting research, data and results must be thoughtfully organized and written to communicate to the medical community, industry, government and other stakeholders. This is the job of the Medical Writer. This role is responsible for researching and writing clinical reports to properly and effectively communicate research and experiments conducted.
Qualified candidates for this line of work must possess a four-year or advanced degree, depending upon the nature and importance of the research/writing to be conducted. Knowledge of clinical procedures and concepts is also required in addition to superior communication and organizational skills.
Employment Outlook
Medical Writer career opportunities are typically 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. Medical Writer positions are expected to increase 10% or more in the next 10 years. Medical Writers earn an average of $23.40 to $37.40 an hour for an annual salary of $48,670 to $77,790 a year or higher, depending on degrees obtained, the research setting, credentials and experience.
Current Job Openings
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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)
Biostatistician
SENIOR BIOSTATISTICIAN
North Wales, PA
Exempt Position
...(more)
Clinical Data Manager
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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)
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 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 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 Coordinator (CRC)
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Provides professional nursing care and monitoring for research patients. Performs duties involved in...(more)
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Clinical Research Associate (CRA)
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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)