Clinical Research Assistant
Quick Apply Full-time 22 hours ago Full Job Description NextStage Clinical Research is seeking an experienced Clinical Research Assistant who is self-motivated, driven and works well with others in a collaborative environment to join our team in the Wichita, KS Area.
NextStage Clinical Research is a fast growing, integrated site management research organization that is partnering with prominent private practice physician groups to deliver innovative healthcare solutions to more patients.
NextStage is poised for accelerated business growth through our experienced team of highly skilled and trained clinical professionals, best in class physicians partners and thought leading leadership team.
Key Job Details:
Competitive compensation & benefits package.
Full-time opportunity with core days/hours M-F 8AM-5PM, and with flexibility to work remotely and in the office.
15% occasional travel nationwide.
Job
Summary:
The CRC will coordinate the execution of all clinical study protocol activities while maintaining GoodClinical Practice (GCP) and adhering to the Food and Drug Administration (FDA) regulations.
The CRC's main responsibility is the conduct of multiple clinical trials, working closely with the Principal Investigator, Sub-Investigators, and support staff.
Essential Duties &
Responsibilities:
1.
Interprets protocol(s) correctly and completely to ensure consistent compliance with applicable standards and related requirements.
2.
Assist in the education of patients and healthcare professionals on the study protocol to ensure complete and correct understanding of information.
3.
Reviews medical records against inclusion/exclusion criteria to identify potential subjects.
4.
Presents information and responds to questions in accordance with standards of professional practice and compliance requirements in relation to matters including, but not limited to, obtaining informed consent.
5.
Maintains and prepares lab kits for subject visits.
6.
Assists coordinators with subject visit and Investigator Team.
7.
Maintains clinical source records.
8.
Organizes Investigator Site Files.
9.
Ensures call notes and documentation is accurate.
10.
Complies with all regulatory requirements, guidelines, and local regulations.
11.
Prepares IRB submissions to include but not limited to development of ICF and any supporting documentation required for submission.
12.
Prepares Regulatory documents per sponsor requirements (FDA Form 1572, Financial Disclosure forms, etc.
).
13.
Coordinates and maintains the following logs:
Delegation of Authority, Deviation Logs, Enrollment, Study Status Logs.
14.
Attends Site Training.
15.
Transcribes source to EDC platforms.
16.
Assists Sponsor and Monitor Visits.
17.
Demonstrates integrity, teamwork, respect, and accountability in all aspects of the job.
18.
Performs job duties and assigned tasks in a safe, efficient, and effective manner, as well as in a manner that is compliant with all company policies, procedures, protocols, and practices.
19.
Perform other duties assigned as it relates to the business needs Minimal Education & Experience Requirements:
High school diploma or equivalent GED Clinical Research Coordinator with Phase 1 and outpatient trials experience One to two years of experience working in a CRC role; or An equivalent combination of education and experience Must be able to provide guidance to research na ve staff Knowledge of protocol and medical terminology Knowledge of regulatory requirements and HIPAA requirements Strong team player with interpersonal skills Must be able to work in a high pace environment Exceptional organizational and time management skills, ability to prioritize task - Detailed oriented Computer Skills (familiar with electronic health record systems, Microsoft Office CCRC Certification preferred, GCP and IATA Physical Requirements & Working Environment:
This position requires frequent sitting, walking, standing, reading, seeing, speaking, hearing, listening, organizing, interpreting data and information, operating office equipment, typing using a computer keyboard, and viewing a computer screen monitor.
The working environment consists of an indoor and climate-controlled setting the majority of the time, and with frequent exposure to a healthcare clinical setting to include, without limitation, frequent potential exposure to blood borne pathogens, and other possible hazards within a clinical setting.
Equal Opportunity Employer Job Type:
Full-time Pay:
$40,000.
00 - $60,000.
00 per year
Benefits:
401(k) 401(k) matching Dental insurance Health insurance Paid time off Vision insurance Schedule:
8 hour shift Monday to Friday Education:
High school or equivalent (Preferred) Work Location:
Hybrid remote in Wichita, KS 67226 Quick Apply.
Estimated Salary: $20 to $28 per hour based on qualifications.
NextStage Clinical Research is a fast growing, integrated site management research organization that is partnering with prominent private practice physician groups to deliver innovative healthcare solutions to more patients.
NextStage is poised for accelerated business growth through our experienced team of highly skilled and trained clinical professionals, best in class physicians partners and thought leading leadership team.
Key Job Details:
Competitive compensation & benefits package.
Full-time opportunity with core days/hours M-F 8AM-5PM, and with flexibility to work remotely and in the office.
15% occasional travel nationwide.
Job
Summary:
The CRC will coordinate the execution of all clinical study protocol activities while maintaining GoodClinical Practice (GCP) and adhering to the Food and Drug Administration (FDA) regulations.
The CRC's main responsibility is the conduct of multiple clinical trials, working closely with the Principal Investigator, Sub-Investigators, and support staff.
Essential Duties &
Responsibilities:
1.
Interprets protocol(s) correctly and completely to ensure consistent compliance with applicable standards and related requirements.
2.
Assist in the education of patients and healthcare professionals on the study protocol to ensure complete and correct understanding of information.
3.
Reviews medical records against inclusion/exclusion criteria to identify potential subjects.
4.
Presents information and responds to questions in accordance with standards of professional practice and compliance requirements in relation to matters including, but not limited to, obtaining informed consent.
5.
Maintains and prepares lab kits for subject visits.
6.
Assists coordinators with subject visit and Investigator Team.
7.
Maintains clinical source records.
8.
Organizes Investigator Site Files.
9.
Ensures call notes and documentation is accurate.
10.
Complies with all regulatory requirements, guidelines, and local regulations.
11.
Prepares IRB submissions to include but not limited to development of ICF and any supporting documentation required for submission.
12.
Prepares Regulatory documents per sponsor requirements (FDA Form 1572, Financial Disclosure forms, etc.
).
13.
Coordinates and maintains the following logs:
Delegation of Authority, Deviation Logs, Enrollment, Study Status Logs.
14.
Attends Site Training.
15.
Transcribes source to EDC platforms.
16.
Assists Sponsor and Monitor Visits.
17.
Demonstrates integrity, teamwork, respect, and accountability in all aspects of the job.
18.
Performs job duties and assigned tasks in a safe, efficient, and effective manner, as well as in a manner that is compliant with all company policies, procedures, protocols, and practices.
19.
Perform other duties assigned as it relates to the business needs Minimal Education & Experience Requirements:
High school diploma or equivalent GED Clinical Research Coordinator with Phase 1 and outpatient trials experience One to two years of experience working in a CRC role; or An equivalent combination of education and experience Must be able to provide guidance to research na ve staff Knowledge of protocol and medical terminology Knowledge of regulatory requirements and HIPAA requirements Strong team player with interpersonal skills Must be able to work in a high pace environment Exceptional organizational and time management skills, ability to prioritize task - Detailed oriented Computer Skills (familiar with electronic health record systems, Microsoft Office CCRC Certification preferred, GCP and IATA Physical Requirements & Working Environment:
This position requires frequent sitting, walking, standing, reading, seeing, speaking, hearing, listening, organizing, interpreting data and information, operating office equipment, typing using a computer keyboard, and viewing a computer screen monitor.
The working environment consists of an indoor and climate-controlled setting the majority of the time, and with frequent exposure to a healthcare clinical setting to include, without limitation, frequent potential exposure to blood borne pathogens, and other possible hazards within a clinical setting.
Equal Opportunity Employer Job Type:
Full-time Pay:
$40,000.
00 - $60,000.
00 per year
Benefits:
401(k) 401(k) matching Dental insurance Health insurance Paid time off Vision insurance Schedule:
8 hour shift Monday to Friday Education:
High school or equivalent (Preferred) Work Location:
Hybrid remote in Wichita, KS 67226 Quick Apply.
Estimated Salary: $20 to $28 per hour based on qualifications.
|
|
 | |
