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View salary and benefits informationManages 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...
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 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, or may need 0 years of experience with additional specialized training and/or certification. 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...
The Clinical Research Programs Manager supervises CRAs in in-house and on-site monitoring, filing, and clinical trial administration. Manages the clinical monitoring process and the administration of clinical trials. Being a Clinical Research Programs Manager helps with the development and implementation of clinical processes, procedures, and programs. Oversees adherence to SOPs, Good Clinical Practice and FDA regulations. In addition, Clinical Research Programs Manager may require ACRP or SOCRA Clinical Research Professional exam completion. May require a master's degree of Nursing. Typically 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...
The Clinical Research Support Administrator selects and observes subjects and assists with data analysis and reporting. Organizes research information for clinical projects. Being a Clinical Research Support Administrator requires a high school diploma or its equivalent. Oversees experiment scheduling and collection of data. In addition, Clinical Research Support Administrator typically reports to a supervisor or manager. Being a Clinical Research Support Administrator gains or has attained full proficiency in a specific area of discipline. Works under moderate supervision. Working as a Clinic more...
The Clinical Research Nurse Leader gathers data and analyzes results. Evaluates, plans, implements, and documents scientific research utilizing human subjects. Being a Clinical Research Nurse Leader requires a bachelor's degree and is certified as a registered nurse. May be responsible for participant recruitment and counseling, ethical oversight, or compilation of study results. In addition, Clinical Research Nurse Leader typically reports to a manager or head of a unit/department. Clinical Research Nurse Leader's years of experience requirement may be unspecified. Certification and/or licens more...
The Clinical Research Project Support Specialist selects and observes subjects and assists with data analysis and reporting. Organizes research information for clinical projects. Being a Clinical Research Project Support Specialist requires a high school diploma or its equivalent. Oversees experiment scheduling and collection of data. In addition, Clinical Research Project Support Specialist typically reports to a supervisor or manager. Being a Clinical Research Project Support Specialist gains or has attained full proficiency in a specific area of discipline. Works under moderate supervision. more...
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