Skip to main content
Tallo logoTallo logo

Find Jobs

Find Jobs Near You – Available Work in Your Location

Skip to job details
Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

Western North Carolina VA Health Care System

Health Sciences Research Study Coordinator

Career Insights for Clinical Coordinator

See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.

Scorecard

Based on North Carolina data

Review key factors to help you decide if this role fits your goals. How is this calculated?

Were these scores useful?

What they do

A Clinical Coordinator coordinates operations and oversees medical assisting staff in a clinic or medical department. Responsibilities include supervision of day-to-day operations, management of business aspects, HR duties within the team.

$66,586 / year median in North Carolina

+25% projected growth

Explore Career

Job Description

Health Sciences Research Specialist/Research Coordinator Are you interested in helping to improve the healthcare of our United States Veterans through meaningful work in a collaborative environment? The Research Service for the Western North Carolina VA Health Care System is hiring full-time Research Coordinators with experience in supporting research clinical trials. This position requires an individual who understands the principles of scientific investigation and clinical trials, is capable of in-depth understanding of the study protocol, and is able to make complex decisions independently. The candidate must possess strong scientific, organizational, and interpersonal skills. Based on the assigned study, the Research Coordinator will provide operational support under the direction of the study's Principal Investigator as well as the Program Specialist for Research & Development.
Key duties:
1. Provide daily operational support 2. Ensure compliance with study protocol, including informed consent, safety, and data security requirements 3. Support research quality control and safety efforts through proper documentation tracking and maintenance 4. Assist with the development of study materials, IRB and R&D documentation and preparing for audits 5. Support recruitment, screening, enrollment, consent, and follow-up of clinical trial participants according to study protocols, including: reviewing medical charts, conducting study visits, administering questionnaires, entering datapoints in a timely and accurate manner, preparing participant mailings, tracking study activities 6. Collect and ship biospecimen ( if appropriate to study design ) 7. Prepare reports, presentations, and data summaries 8.
Manage team meetings including:
arranging meetings, taking meeting notes, entering data, maintaining quality control of data, coordinating research mailings, and other research support duties 9. Assist with development and maintenance of databases and files 10. Assist with grant submissions, including preparing applications, conducting literature reviews, and other tasks as needed
Qualifications:
1. Must have Bachelor of Science degree or Masters in Public 2. 2-4 years of work experience in clinical or health services research required a. If
BA/BS, 2-4
years of research-related experience required b. If higher degree, 1-2 years of research-related experience preferred 3. Excellent communication and interpersonal skills with the ability to collaborate with a diverse group of researchers and staff 4. Experience with customer service, particularly by telephone and e-mail 5. Strong attention to detail and organizational skills 6. Solid problem-solving and critical thinking skills 7. Excellent time management skills 8. Ability to adapt to changing priorities and timelines 9. Ability to work independently with minimal supervision 10. Proficiency in Microsoft Word, Excel, PowerPoint, and Outlook required 11. Experience with Microsoft Access, Microsoft SharePoint, and Microsoft Teams preferred 12. Experience with using electronic medical record systems 13. Knowledge of research compliance regulations 14.
Phlebotomy experience preferred Application information:
Candidates must be U.S. citizens. Education and experience will be evaluated to determine if the top candidate meets the criteria for the targeted GS-09 or GS-11 and commensurate with experience. Please send a resume to paula.taylor6@va.gov. Applications will be accepted until the positions are filled. Diversity enriches research and promotes the best healthcare. We are committed to building and sustaining an equitable and inclusive environment. We encourage individuals whose backgrounds or interests align with this commitment, as well as individuals from all backgrounds that are underrepresented in research, to apply.
Job Type:
Full-time Pay:
From Benefits:
401(k) Dental insurance Employee assistance program Health insurance Paid time off Parental leave Vision insurance
Schedule:
8-hour shift Monday to Friday Ability to commute/relocate: Asheville, NC (28805): Reliably commute or planning to relocate before starting work
Education:
Minimum:
Bachelor of Science degree or Masters in
Public Experience:
Clinical Research Coordinator:
1 year (Required)
Work Location:
In person with some telework.
Job Type:
Full-time Pay:
$75,000.00 - $95,000.00 per year
Benefits:
401(k) Dental insurance Employee assistance program Health insurance Paid time off Parental leave Vision insurance
Education:
Bachelor's (Preferred) Ability to
Relocate:
Asheville, NC 28805: Relocate before starting work (Required)
Work Location:
Hybrid remote in Asheville, NC 28805