What are the responsibilities and job description for the HVI Research Assistant position at West Virginia University Hospital, Inc?
MINIMUM QUALIFICATIONS:
EDUCATION, CERTIFICATION, AND/OR LICENSURE:
1. Bachelor's Degree.
EXPERIENCE:
1. One year of experience in research, administrative, or clinical support.
PREFERRED QUALIFICATIONS:
EDUCATION, CERTIFICATION, AND/OR LICENSURE:
1. Obtain certification as a Research Professional through the Society of Clinical Research Associates (SoCRA)ORthe Association of Clinical Research Professionals (ACRP) with three years of hire date preferred.
EXPERIENCE:
1. One year of experience in healthcare.
2. Two years of experience in research, administrative, or clinical support.
CORE DUTIES AND RESPONSIBILITIES:The statements described here are intended to describe the general nature of work being performed by people assigned to this position. They are not intended to be constructed as an exhaustive list of all responsibilities and duties. Other duties may be assigned.
1. Assists in study enrollment and specimen collection as needed.
2. Assists with data collection and checking data completeness.
3. Assists with follow-up mailings and phone calls to ensure the Follow-Up Protocol is utilized.
4. Assists in reviewing the data collection forms for completeness and reconciling missing data for data entry.
5. Enters research/project data into databases, ensuring data accuracy, and timeliness of data entry.
6. Produces documents accurately and in a timely manner, corrected for content and grammar according to project timeline.
7. Demonstrates the ability to obtain patient information from computer applications in an accurate and timely manner.
8. Utilizes computer software and Internet access to assist the research team in planning, scheduling, and conducting meetings, presentations, and conferences.
9. Utilizes computer software and Internet access to assist the research team in preparing abstracts and manuscripts.
10. Maintains well organized files for reference in the work of the project.
11. Clearly and consistently communicates status of projects to research team members.
12. Demonstrates the ability to raise questions and seek additional information as necessary to complete job responsibilities.
13. Familiarize and become highly knowledgeable with all study/clinical trials protocols currently assigned to the department.
14. Participates in a variety of complex activities involved in the collection, compilation, documentation and analysis of clinical research data.
15. Performs filing and data entry as needed to keep all research records and regulatory files up to date.
16. Work collaboratively with investigators and study coordinators for study-specific training and communication related to possible or already accrued study participants.
17. Independently participates in activities to increase knowledge base and performance.
19. Ensures compliance with WVU Institutional Review Board, Good Clinical Practice guidelines and federal regulations related to clinical research.
20. Maintains timely, study-specific documentation that reflects an accurate, complete, and legible record of study activities.
21. Associated clerical duties as assigned and necessary for each study/trial assigned.
22. Attendance of all appropriate training seminars as required by study/trial agency.
PHYSICAL REQUIREMENTS:The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
1. Requires Manual dexterity used in operating office equipment.
2. Requires Standing and bending in the assessment and treatment of patients.
3. Prolonged periods of sitting and the ability to walk moderate distances.
4. Some manual work may be included; occasional heavy lifting (patient assistance) and the ability to move equipment.
WORKING ENVIRONMENT:The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
1. Normal, clinical environment. There is patient contact and potential to come in contact with patients having communicable disease (URI, HIV, Hepatitis B, TB, usual childhood diseases, etc.) The presence of blood and specimen care and processing is a routine part of this environment.
SKILLS AND ABILITIES:
1. Prior clinical research and trial experience desired.
2. Excellent written, oral, and interpersonal communication skills.
3. High degree of computer literacy, MS Office products.
4. Planning skills in scheduling of patients, physicians, site visitors and facility usage are critical. Analysis of protocols, feasibility of studies based on patient populations, financial considerations, facility capabilities, technical support and other support systems is imperative.
5. Ability to work independently.
6. Analytical skills include the technical aspects of gathering data for purposes of study-related activities.
7. Careful attention to detail.
8. Excellent organization skills and ability to prioritize a variety of tasks.
MINIMUM QUALIFICATIONS:
EDUCATION, CERTIFICATION, AND/OR LICENSURE:
1. Bachelor's Degree.
EXPERIENCE:
1. One year of experience in research, administrative, or clinical support.
PREFERRED QUALIFICATIONS:
EDUCATION, CERTIFICATION, AND/OR LICENSURE:
1. Obtain certification as a Research Professional through the Society of Clinical Research Associates (SoCRA)ORthe Association of Clinical Research Professionals (ACRP) with three years of hire date preferred.
EXPERIENCE:
1. One year of experience in healthcare.
2. Two years of experience in research, administrative, or clinical support.
CORE DUTIES AND RESPONSIBILITIES:The statements described here are intended to describe the general nature of work being performed by people assigned to this position. They are not intended to be constructed as an exhaustive list of all responsibilities and duties. Other duties may be assigned.
1. Assists in study enrollment and specimen collection as needed.
2. Assists with data collection and checking data completeness.
3. Assists with follow-up mailings and phone calls to ensure the Follow-Up Protocol is utilized.
4. Assists in reviewing the data collection forms for completeness and reconciling missing data for data entry.
5. Enters research/project data into databases, ensuring data accuracy, and timeliness of data entry.
6. Produces documents accurately and in a timely manner, corrected for content and grammar according to project timeline.
7. Demonstrates the ability to obtain patient information from computer applications in an accurate and timely manner.
8. Utilizes computer software and Internet access to assist the research team in planning, scheduling, and conducting meetings, presentations, and conferences.
9. Utilizes computer software and Internet access to assist the research team in preparing abstracts and manuscripts.
10. Maintains well organized files for reference in the work of the project.
11. Clearly and consistently communicates status of projects to research team members.
12. Demonstrates the ability to raise questions and seek additional information as necessary to complete job responsibilities.
13. Familiarize and become highly knowledgeable with all study/clinical trials protocols currently assigned to the department.
14. Participates in a variety of complex activities involved in the collection, compilation, documentation and analysis of clinical research data.
15. Performs filing and data entry as needed to keep all research records and regulatory files up to date.
16. Work collaboratively with investigators and study coordinators for study-specific training and communication related to possible or already accrued study participants.
17. Independently participates in activities to increase knowledge base and performance.
19. Ensures compliance with WVU Institutional Review Board, Good Clinical Practice guidelines and federal regulations related to clinical research.
20. Maintains timely, study-specific documentation that reflects an accurate, complete, and legible record of study activities.
21. Associated clerical duties as assigned and necessary for each study/trial assigned.
22. Attendance of all appropriate training seminars as required by study/trial agency.
PHYSICAL REQUIREMENTS:The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
1. Requires Manual dexterity used in operating office equipment.
2. Requires Standing and bending in the assessment and treatment of patients.
3. Prolonged periods of sitting and the ability to walk moderate distances.
4. Some manual work may be included; occasional heavy lifting (patient assistance) and the ability to move equipment.
WORKING ENVIRONMENT:The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
1. Normal, clinical environment. There is patient contact and potential to come in contact with patients having communicable disease (URI, HIV, Hepatitis B, TB, usual childhood diseases, etc.) The presence of blood and specimen care and processing is a routine part of this environment.
SKILLS AND ABILITIES:
1. Prior clinical research and trial experience desired.
2. Excellent written, oral, and interpersonal communication skills.
3. High degree of computer literacy, MS Office products.
4. Planning skills in scheduling of patients, physicians, site visitors and facility usage are critical. Analysis of protocols, feasibility of studies based on patient populations, financial considerations, facility capabilities, technical support and other support systems is imperative.
5. Ability to work independently.
6. Analytical skills include the technical aspects of gathering data for purposes of study-related activities.
7. Careful attention to detail.
8. Excellent organization skills and ability to prioritize a variety of tasks.
Additional Job Description:
Scheduled Weekly Hours:
40Shift:
Days (United States of America)Exempt/Non-Exempt:
United States of America (Non-Exempt)Company:
WVUH West Virginia University HospitalsCost Center:
7917 UHA HVI IND Sponsored ResearchAddress:
1 Medical Center DriveMorgantownWest VirginiaEqual Opportunity Employer/Protected Veterans/Individuals with Disabilities.
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The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. 41 CFR 60-1.35(c)
