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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...
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 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...
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.
Participates in research and development activities. Utilizes established mathematical and scientific techniques to compile and analyze data. Writes technical reports detailing procedures, outcomes, and observations. May require a master's degree. Typically reports to a supervisor or manager. Work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. Typically requires 4-7 years of related experience. more...
The Scientific Research Associate III utilizes established mathematical and scientific techniques to compile and analyze data. Participates in research and development activities. Being a Scientific Research Associate III requires an advanced degree. Writes technical reports detailing procedures, outcomes, and observations. In addition, Scientific Research Associate III typically reports to a supervisor or manager. Being a Scientific Research Associate III contributes to moderately complex aspects of a project. Work is generally independent and collaborative in nature. Working as a Scientific more...
The Research Associate III - Academic makes detailed observations, analyzes data, and interprets results. Carries out research/development activities. Being a Research Associate III - Academic conducts research, writes substantive policy papers, collaborates with lead researchers with respect to larger or more complex studies. Compiles results and prepares technical reports and documentation of outcomes. In addition, Research Associate III - Academic requires a master's degree. Typically reports to a supervisor or manager. Research Associate III - Academic is a specialist on complex technical more...
The Research Associate, Healthcare III reports to management on key findings of research initiatives conducted for major biotechnology, pharmaceutical, and healthcare organizations. Typically leads a research team. Being a Research Associate, Healthcare III typically reports to a supervisor or manager. May require a bachelor's/master's degree. Working as a Research Associate, Healthcare III typically requires 4 to 7 years of related experience. Contributes to moderately complex aspects of a project. Work is generally independent and collaborative in nature. more...
The Research Associate, Pharma III reports to management on key findings of research initiatives conducted for major biotechnology, pharmaceutical, and healthcare organizations. Typically leads a research team. Being a Research Associate, Pharma III typically reports to a supervisor or manager. May require a bachelor's/master's degree. Working as a Research Associate, Pharma III typically requires 4 to 7 years of related experience. Contributes to moderately complex aspects of a project. Work is generally independent and collaborative in nature. more...
The Clinical Trials Research Associate I analyzes and evaluates clinical data gathered during research. Participates in the design, administration and monitoring of clinical trials. Being a Clinical Trials Research Associate I knowledge of FDA regulatory requirements is required. Ensures compliance with protocol and overall clinical objectives. In addition, Clinical Trials 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 Trials more...
The Clinical Trials Research Associate II analyzes and evaluates clinical data gathered during research. Participates in the design, administration and monitoring of clinical trials. Being a Clinical Trials Research Associate II knowledge of FDA regulatory requirements is required. Ensures compliance with protocol and overall clinical objectives. In addition, Clinical Trials Research Associate II 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. Being a Clinical Trials Res more...
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