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View salary and benefits informationOrganizes 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 equivalent. Typically reports to a supervisor or manager. Works under moderate supervision. Gaining or has attained full proficiency in a specific area of discipline. Typically requires 1-3 years of related experience. more...
The Clinical Research Records Management Coordinator ensures all medical records are tracked and released according to HIPAA guidelines. Responsible for organizing and overseeing the record keeping activities pertaining to releasing and retrieving medical records for research projects. Being a Clinical Research Records Management Coordinator typically reports to a supervisor or manager. May require an associate's degree or its equivalent. Being a Clinical Research Records Management Coordinator possesses a moderate understanding of general aspects of the job. Works under the close direction of more...
Responsible for organizing and overseeing the record keeping activities pertaining to releasing and retrieving medical records for research projects. Ensures all medical records are tracked and released according to HIPAA guidelines. May require an associate degree or its equivalent. Typically reports to a supervisor or manager. Possesses a moderate understanding of general aspects of the job. Works under the close direction of senior personnel in the functional area. May require 0-1 year of general work experience. more...
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 a master's degree in nursing. May require ACRP or SOCRA Clinical Research Professional exam completion. Typically reports to a director. Manages subordinate staff in the day-to-day performance of their jobs. True first level manager. Ensures t more...
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...
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...
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...
The Clinical Research Pharmacist monitors patient data on drug therapies outcomes, reactions, and errors. Directs and develops research of existing and new prescription drugs and conducts utilization reviews to develop guidelines for usage, prior authorization, and updates to formulary. Being a Clinical Research Pharmacist administers a prior authorization program. Provides education and outreach to medical staff on prescribing guidelines, alternative drug therapies, and risk mitigation. In addition, Clinical Research Pharmacist requires a Ph.D. of Doctor of Pharmacy (Pharm.D.). Typically repo 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...
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...
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