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Alternate job titles: Clinical Trails Research Associate I | Clinical Trials Data Analyst I

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...



Alternate job titles: Clinical Trails Research Associate II | Clinical Trials Data Analyst II

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. Occasionally directed in several aspects of the work. Gains exposure to some of the complex tasks within the job function. Typically requires 2 -4 years of rela more...


Alternate job titles: Clinical Trails Research Associate II | Clinical Trials Data Analyst II

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.


Alternate job titles: Clinical Research Associate I | Clinical Trials Data Analyst I

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...



Alternate job titles: Clinical Research Associate II | Clinical Trials Data Analyst II

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...


Alternate job titles: Clinical Research Programs Director

Directs and oversees the clinical research function for a healthcare organization. Develops research studies and creates standards and guidelines for clinical research services and programs. Ensures adherence to standard operating procedures, good clinical practice and FDA regulations. Requires an advanced degree. Typically reports to top management. Manages a departmental sub-function within a broader departmental function. Creates functional strategies and specific objectives for the sub-function and develops budgets/policies/procedures to support the functional infrastructure. Deep knowledg more...



Alternate job titles: Clinical Research Programs Manager

Manages the clinical monitoring process and the administration of clinical trials. Supervises CRAs in in-house and on-site monitoring, filing, and clinical trial administration. Oversees adherence to SOPs, Good Clinical Practice and FDA regulations. Helps with the development and implementation of clinical processes, procedures, and programs. May require ACRP or SOCRA Clinical Research Professional exam completion. May require a master's degree of Nursing. Typically reports to top management. Manages subordinate staff in the day-to-day performance of their jobs. True first level manager. Ensur more...


Alternate job titles: Clinical Research Lead Scientist | Senior Clinical Researcher

Assumes lead role in various clinical research projects. Proposes, plans, organizes and executes experiments and research. Secures grants and funding for research and is responsible for controlling budgets. Summarizes findings in reports and communicates results. Interacts with other scientists within and outside of the organization. Provides recommendations that influence extensive clinical research activities. Requires an advanced degree. Typically reports to head of a unit/department. Work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a p more...


Alternate job titles: Clinical Research Assistant | Clinical Research Project Support Specialist | Clinical Research Support Administrator

Organizes research information for clinical projects. Selects and observes subjects and assists with data analysis and reporting. Oversees experiment scheduling and collection of data. Requires a high school diploma or its equivalent. Typically reports to a supervisor or manager. Gains or has attained full proficiency in a specific area of discipline. Works under moderate supervision. Typically requires 1-3 years of related experience. more...



Alternate job titles: Clinical Research Coordinator | Clinical Research Project Support Specialist | Clinical Research Support Administrator

The Clinical Research Assistant selects and observes subjects and assists with data analysis and reporting. Organizes research information for clinical projects. Being a Clinical Research Assistant requires a high school diploma or its equivalent. Oversees experiment scheduling and collection of data. In addition, Clinical Research Assistant typically reports to a supervisor or manager. Being a Clinical Research Assistant gains or has attained full proficiency in a specific area of discipline. Works under moderate supervision. Working as a Clinical Research Assistant typically requires 1-3 yea more...


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