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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 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

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 Ethics Specialist

Offers guidance to patients, their families, and professional staff on ethical, legal and policy issues and concerns stemming from clinical interactions between health care professionals and patients. Provides guidance to the institutional ethics committee pertaining to policy formulation and educational and case review activities. Develops institutional policies concerning ethical issues such as "do-not-resuscitate" and "withdrawal of life-support". Requires a master's degree or doctorate related to health ethics. Typically reports to a manager or head of a unit/department. Typically requires more...



Alternate job titles: Clinical Research Coordinator | Clinical Research Assistant | Clinical Research Support Administrator

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...


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: Licensed Medical Esthetician

The Clinical Esthetician performs procedures such as skin evaluation, facial massages, and hair removal. Delivers skin care treatments and provides consultations with makeup applications and purchases. Being a Clinical Esthetician may require an associate degree. Supports dermatologists and plastic surgeons on patients preoperative and postoperative exams. In addition, Clinical Esthetician typically reports to a supervisor. Requires a state license to practice. Clinical Esthetician's years of experience requirement may be unspecified. Certification and/or licensing in the position's specialty more...


Alternate job titles: Quality Assurance Nurse, Sr. | Patient Care Quality Improvement and Compliance Nurse II | Senior Patient Care Quality Evaluator (RN)

The Senior Clinical Care Quality Evaluator (RN) monitors compliance with current laws, process improvements, and implementation of clinical best practices. Evaluates the quality of patient care. Being a Senior Clinical Care Quality Evaluator (RN) helps train staff on new or improved clinical practices. Reviews and analyzes customer complaints. In addition, Senior Clinical Care Quality Evaluator (RN) requires an associate's degree/bachelor's degree and is licensed to practice nursing. Typically reports to a manager or head of a unit/department. Working as a Senior Clinical Care Quality Evaluato 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...


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