Clinical Research Coordinator I
Duties:
Position Purpose This position assists in managing clinical research studies and is responsible for the efficient coordination of clinical studies by working closely with clinical investigators, physicians, department managers and others.
Scope Essential Job Duties Requires Moderate Supervision Has demonstrated success in the following:
o Assist in building and maintaining study samples.
o Disseminate information about the project.
o Screen participants by assessing eligibility for research protocols and potential for commitment to project.
o Develop and implement recruitment enhancement strategies.
o Monitor participant progression throughout study and conduct evaluation at end of study.
o Coordinate clinical patient information according to research protocols and assist the physician or residents with gathering pertinent clinical information.
o Trains techniques of clinical research coordination and practices, FDA Good Clinical Practices (GCP), and clinical research standard operating procedures to ensure compliance with policy and procedure, research sponsors and Federal rules and regulations.
o Safely operate laboratory equipment and comply with all regulations.
Skills:
Minimum RequirementsThree years of clinical research experience.
Experience using basic computer programs including word processing, database, spreadsheet applications and e-mail.
Experience using laboratory protocol, systems and documentation techniques.
Physical RequirementsOngoing need for employee to see and read information, labels, monitors, etc.
and to see to identify equipment and supplies and to utilize a wide variety of information including organizing and completing documentation and forms, accessing and entering computer information, and identifying needs and urgent issues.
Frequent interactions with patient care providers, patients, and visitors that require employee to verbally communicate as well as hear and understand spoken information, alarms, needs, and issues quickly and accurately.
Manual dexterity of hands and fingers to manipulate complex and delicate equipment with precision and accuracy.
This includes frequent computer use and typing for documenting patient interactions, accessing needed information, operating telephones and other office equipment, including manipulating paper - requiring the ability to move fingers and hands.
Expected to bend, lift, and carry patient files, documents, equipment, and supplies.
Remain sitting or standing for long periods of time while interacting with others or to perform work on a computer, telephone, or other equipment.
KeywordsEducation:
referred Qualifications Bachelor's Degree or higher from an accredited institution.
Prior experience in healthcare.
Skills and ExperienceRequired SkillsCLINICAL RESEARCH Recommended Skills Alarm Devices Audio Equipments Clinical Research Clinical Research Coordination Clinical Works Databases Estimated Salary: $20 to $28 per hour based on qualifications.
Position Purpose This position assists in managing clinical research studies and is responsible for the efficient coordination of clinical studies by working closely with clinical investigators, physicians, department managers and others.
Scope Essential Job Duties Requires Moderate Supervision Has demonstrated success in the following:
o Assist in building and maintaining study samples.
o Disseminate information about the project.
o Screen participants by assessing eligibility for research protocols and potential for commitment to project.
o Develop and implement recruitment enhancement strategies.
o Monitor participant progression throughout study and conduct evaluation at end of study.
o Coordinate clinical patient information according to research protocols and assist the physician or residents with gathering pertinent clinical information.
o Trains techniques of clinical research coordination and practices, FDA Good Clinical Practices (GCP), and clinical research standard operating procedures to ensure compliance with policy and procedure, research sponsors and Federal rules and regulations.
o Safely operate laboratory equipment and comply with all regulations.
Skills:
Minimum RequirementsThree years of clinical research experience.
Experience using basic computer programs including word processing, database, spreadsheet applications and e-mail.
Experience using laboratory protocol, systems and documentation techniques.
Physical RequirementsOngoing need for employee to see and read information, labels, monitors, etc.
and to see to identify equipment and supplies and to utilize a wide variety of information including organizing and completing documentation and forms, accessing and entering computer information, and identifying needs and urgent issues.
Frequent interactions with patient care providers, patients, and visitors that require employee to verbally communicate as well as hear and understand spoken information, alarms, needs, and issues quickly and accurately.
Manual dexterity of hands and fingers to manipulate complex and delicate equipment with precision and accuracy.
This includes frequent computer use and typing for documenting patient interactions, accessing needed information, operating telephones and other office equipment, including manipulating paper - requiring the ability to move fingers and hands.
Expected to bend, lift, and carry patient files, documents, equipment, and supplies.
Remain sitting or standing for long periods of time while interacting with others or to perform work on a computer, telephone, or other equipment.
KeywordsEducation:
referred Qualifications Bachelor's Degree or higher from an accredited institution.
Prior experience in healthcare.
Skills and ExperienceRequired SkillsCLINICAL RESEARCH Recommended Skills Alarm Devices Audio Equipments Clinical Research Clinical Research Coordination Clinical Works Databases Estimated Salary: $20 to $28 per hour based on qualifications.
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