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View salary and benefits informationParticipates in the design, administration and monitoring of clinical trials. Analyzes and evaluates clinical data gathered during research. Ensures compliance with protocol and overall clinical objectives. Knowledge of FDA regulatory requirements is required. May require ACRP or SOCRA Clinical Research Professional exam completion. Requires a master's degree in science or equivalent. Typically reports to a supervisor or manager. Occasionally directed in several aspects of the work. Gaining exposure to some of the complex tasks within the job function. Typically requires 2-4 years of related e more...
Participates in the design, administration and monitoring of clinical trials. Analyzes and evaluates clinical data gathered during research. Ensures compliance with protocol and overall clinical objectives. Knowledge of FDA regulatory requirements is required. May require ACRP or SOCRA Clinical Research Professional exam completion. Requires a bachelor's degree in Science or its equivalent. Typically reports to a supervisor or manager. Work is closely managed. Works on projects/matters of limited complexity in a support role. Typically requires 0-2 years of related experience. more...
There is currently no job description for Senior Clinical Research Associate. Be the first to submit the job responsibilities for a Senior Clinical Research Associate.
The Clinical Trails Research Associate I analyzes and evaluates clinical data gathered during research. Participates in the design, administration and monitoring of clinical trials. Being a Clinical Trails Research Associate I knowledge of FDA regulatory requirements is required. Ensures compliance with protocol and overall clinical objectives. In addition, Clinical Trails Research Associate I may require ACRP or SOCRA Clinical Research Professional exam completion. Requires a bachelor's degree in Science or its equivalent. Typically reports to a supervisor or manager. Being a Clinical Trails more...
The Clinical Trails Research Associate II analyzes and evaluates clinical data gathered during research. Participates in the design, administration and monitoring of clinical trials. Being a Clinical Trails Research Associate II knowledge of FDA regulatory requirements is required. Ensures compliance with protocol and overall clinical objectives. In addition, Clinical Trails Research Associate II may require ACRP or SOCRA Clinical Research Professional exam completion. Requires a bachelor's degree in Science or its equivalent. Typically reports to a supervisor or manager. Being a Clinical Trai more...
The R & D Support Associate I utilizes established mathematical and scientific techniques to compile and analyze data. Participates in research and development activities. Being a R & D Support Associate I requires a bachelor's degree. Writes technical reports detailing procedures, outcomes, and observations. In addition, R & D Support Associate I typically reports to a supervisor or manager. Being a R & D Support Associate I works on projects/matters of limited complexity in a support role. Work is closely managed. Working as a R & D Support Associate I typically requires 0-2 years of related more...
The R & D Support Associate II utilizes established mathematical and scientific techniques to compile and analyze data. Participates in research and development activities. Being a R & D Support Associate II requires a bachelor's degree. Writes technical reports detailing procedures, outcomes, and observations. In addition, R & D Support Associate II typically reports to a supervisor or manager. Being a R & D Support Associate II gains exposure to some of the complex tasks within the job function. Occasionally directed in several aspects of the work. Working as a R & D Support Associate II typ more...
The R & D Support Associate III utilizes established mathematical and scientific techniques to compile and analyze data. Participates in research and development activities. Being a R & D Support Associate III requires an advanced degree. Writes technical reports detailing procedures, outcomes, and observations. In addition, R & D Support Associate III typically reports to a supervisor or manager. Being a R & D Support Associate III contributes to moderately complex aspects of a project. Work is generally independent and collaborative in nature. Working as a R & D Support Associate III typical more...
The R & D Support Associate IV utilizes established mathematical and scientific techniques to compile and analyze data. Participates in research and development activities. Being a R & D Support Associate IV requires an advanced degree. Writes technical reports detailing procedures, outcomes, and observations. In addition, R & D Support Associate IV typically reports to a manager or head of a unit/department. R & D Support Associate IV is a specialist on complex technical and business matters. Work is highly independent. May assume a team lead role for the work group. Working as a R & D Suppor more...
The R & D Support Associate V utilizes established mathematical and scientific techniques to compile and analyze data. Participates in research and development activities. Being a R & D Support Associate V requires an advanced degree. Writes technical reports detailing procedures, outcomes, and observations. In addition, R & D Support Associate V typically reports to a manager or head of a unit/department. Being a R & D Support Associate V works on advanced, complex technical projects or business issues requiring state of the art technical or industry knowledge. Works autonomously. Goals are g more...
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