Permanent Staff (SHRA)Is this an internal only recruitment?:
Soc/Clin Research Specialist - ContributingWorking Title:
Research CoordinatorPosition Number:
P012883Budgeted Hiring Range:
$42,623 - $55,160Pay Band Information:
To learn more about the pay band for this branch and role, please see the Career Banding rates spreadsheet.Salary Grade Equivalent:
Full-Time Time-LimitedIf time-limited, estimated duration of appointment:
3 yearsHours per week:
Monday-Friday between the hours of 7:30am and 7:30pm, weekends possible
(schedule requires some flexibility and is subject to change depending on study needs).Department Name and Number:
Globl Hlth and Infect Disease-427801Date First Posted:
Chapel Hill, NCPosition Posting Category:
Research ProfessionalsDepartment Description:
The Institute for Global Health and Infectious Disease (IGHID) conducts investigator-initiated, industry-funded, NIH funded AIDS prevention and treatment, sexually transmitted infections, other infectious diseases scientific and clinical research, and provides patient care at UNC-Chapel Hill and at sites throughout the world. The University of North Carolina’s Global HIV Prevention and Treatment Clinical Trials Unit is dedicated to developing and conducting research on HIV prevention, HIV infection, HIV-associated opportunistic infections, and complications of HIV therapy, as well as conducting research in other infectious diseases including COVID-19.Equal Opportunity Employer:
The University of North Carolina at Chapel Hill is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to age, color, disability, gender, gender expression, gender identity, genetic information, race, national origin, religion, sex, sexual orientation, or status as a protected veteran.Position Description:
THIS IS A TIME LIMITED POSITION WITH AN ESTIMATED DURATION OF 3 YEARS.
The Research Coordinator is responsible for the implementation of clinical trials involving two potentially fatal diseases within the UNC Global HIV Prevention and Treatment Clinical Trials Unit and UNC’s COVID-19 Research Response. The Research Coordinator must have a broad knowledge of HIV/AIDS, COVlD-19, medical ethics, Good Clinical Practice (GCP) as well as network and study-specific procedures and data collection. The Research Coordinator is a professional member of the staff and as such is expected to work independently, adhere to all University, CTU, and profession-specific regulations, participate in unit-wide activities and exhibit a high degree of accountability for all work.
The Research Coordinator will coordinate initial staff orientation and conduct and maintain the records for training associated with various support staff responsibilities (HIV rapid testing, Neurocognitive Assessments, Anthropometric Measurements, Frailty Testing). The person in this role will also provide administrative and clinical support to Investigators of Record, the Research Coordinator(s), and other research team members in their work.
This position will also be responsible for data and specimen collection and shipment, maintenance of electronic and paper-based research records and regulatory documents in accordance with Federal, State, and local regulations, as well as GCP. This position may also be responsible for other duties as assigned. These duties include preparing and scheduling participant visits, performing evaluations within the scope of the position, and general office administrative tasks.Minimum Education and Experience Requirements:
Bachelor’s degree in a discipline related to the field assigned and one year of related training or experience; or equivalent combination of training and experience. All degrees must be received from appropriately accredited institutions.Essential Skills, Knowledge and Abilities:
Candidates must have the ability to communicate effectively and respectfully with volunteers, patients, families, staff physicians, and/or sponsor representatives from diverse backgrounds and sexual and racial identities.
This position requires the ability to work independently and efficiently in a fast-paced environment. Instructions are given verbally and/or in writing.
Microsoft WORD, EXCEL, email, and internet navigation skills required.
Must have the ability to multitask and reorganize tasks according to shifting priorities.
This individual must have the ability to maintain team, unit, and university goals while meeting or exceeding individual work goals and have the ability to meticulously perform all study-related functions while maintaining a high level of organization.
Must be willing and able to commute to clinical research sites in Greensboro, Raleigh, and Chapel Hill, NC.
A valid Driver’s license is required
Bloodborne pathogen training required (will be provided).Preferred Qualifications:
Phlebotomy training preferred.
Previous experience with target populations preferred.
Preference for candidates that have excellent communication skills with diverse participant and staff populations and have the ability to appreciate and maintain confidentiality at all times.
Knowledge and experience with Clinical Research are highly preferred.Required Licenses/Certifications:
Valid NC driver’s licensePosition/Schedule Requirements:
Exposure to Bloodborne Pathogens, Valid NC Driver’s LicenseStimulus/ARRA Funded: