UTS - Temporary Sr. Clinical Research Coordinator at UNC Chapel Hill
University of North Carolina at Chapel Hill

Chapel Hill, North Carolina
$0.00 - $100.00 per hour


Department:

HR UTS Partnership

Career Area :

Research Professionals

Posting Open Date:

11/07/2024

Application Deadline:

11/29/2024

Position Type:

Temporary Staff (SHRA)

Position Title :

UTS - Temporary Sr. Clinical Research Coordinator at UNC Chapel Hill

Vacancy ID:

S024295

Full-time/Part-time:

Full-Time Temporary

Work Schedule:

Monday - Friday, 8am - 5pm, 3 days in office- 2 days remote per week

Hiring Range:

$44.00 per hour

Proposed Start Date:

11/18/2024

Estimated Duration of Appointment:

3 months or less

Be a Tar Heel!:

A global higher education leader in innovative teaching, research and public service, the University of North Carolina at Chapel Hill consistently ranks as one of the nation's top public universities. Known for its beautiful campus, world-class medical care, commitment to the arts and top athletic programs, Carolina is an ideal place to teach, work and learn.One of the best college towns and best places to live in the United States, Chapel Hill has diverse social, cultural, recreation and professional opportunities that span the campus and community.University employees can choose from a wide range of professional training opportunities for career growth, skill development and lifelong learning and enjoy exclusive perks that include numerous retail and restaurant discounts, savings on local child care centers and special rates for performing arts events.

Position Summary:

This position will serve as a Senior Clinical Research Coordinator with the Better Tomorrow Network within the Institute for Trauma Recovery (Department of Psychiatry). The Senior Clinical Research Coordinator is responsible for the planning, organization, conduct, and evaluation of multi-faceted clinical research protocols, including study execution, developing strategies and solutions to improve study processes and execution, providing reviews of other team members' work product, and serving as a mentor and subject matter expert.

The Institute for Trauma Recovery seeks to advance understanding of trauma recovery and develop interventions that improve recovery. The foundation of our success is our fantastic team of faculty and staff. Our team believes that achieving new discoveries for trauma survivors around the globe, via observational studies and randomized controlled trials, is an extremely meaningful and satisfying way to spend one's professional life. We work to place the trauma survivor at the center of all of our decisions and to serve them through our work. We continuously work to create a community where our team members serve trauma survivors and actualize their career growth and individual leadership potential.

BTN is the first research network in the world dedicated to improving treatments and care for survivors of sexual assault. BTN's mission is to remove barriers to the conduct of high-quality, large-scale research studies that improve survivors' lives. The goal of BTN is to greatly increase the number of studies of survivors performed, so that the care of survivors is steadily improved. Through collaborations with sexual assault treatment centers, researchers, stakeholders, and survivors, and through the use of the BTN National Research Volunteer Registry, BTN supports a range of interdisciplinary studies that focus on innovative approaches to prevention, early intervention, and treatment. BTN's long-term vision is to contribute to achieving the goal that one day no survivor will experience chronic reductions in physical health, mental health, or quality of life due to sexual assault, and that perpetrators will be fairly brought to justice within a survivor-supporting system.

The BTN Coordinator will independently provide clinical research administration and study coordination. The Coordinator will work alongside the BTN Manager and PI to advance BTN's mission, and will help manage research staff and student volunteers working on BTN studies. This position will be responsible for a broad range of duties related to planning, organizing, executing, and monitoring the implementation of new and existing studies and other research initiatives.

Duties will include supporting the PI and BTN Manager with maintaining research methods, tracking patients in the study, providing feedback and suggestions on the development/revision of research protocols and regulatory correspondence, and maintaining accurate and updated manuals of procedures for the studies. This position will serve as lead coordinator on one or more BTN studies. The Coordinator will also help oversee the network of partnering sites and contribute to the identification, selection, and negotiation of additional sites and studies, ensuring that partnering sites have the skill level and availability necessary to properly conduct the research. This position will also ensure that BTN staff are adhering to the appropriate SOPs and achieving excellence in patient/participant care.

Due to the nature of the research (sexual assault) and the geographical spread of study sites across time zones, typical encounters are after business hours and on the weekends, therefore it is typical that the position will provide support, respond when a potential research subject has been identified and make decisions

Minimum Education and Experience Requirements:

Bachelor's Degree in a related discipline and five years experience

Required Qualifications, Competencies, and Experience:

  • Specialized knowledge in clinical research principles.
  • Ability to plan and design methodologies for monitoring data collection.
  • Ability to take a leadership role in implementing changes in design of clinical research management.
  • Ability to problem solve and resolve quality control issues by changing processes.
  • Strong written and verbal communication skills.
  • Must be able to work and communicate with diverse populations effectively and professionally.
  • Ability to work independently as well as function as part of a team.
  • Proficient with Microsoft Outlook, Excel, and Word.
  • Must have experience working with human subjects in research studies
  • Must have strong project management/project coordinator experience as it relates to clinical research

Preferred Qualifications, Competencies, and Experience:

Master's degree or higher in health services research, exercise and sports science, public health, epidemiology or a related field. Experience in human-subjects research is critical. Excellent written and oral communication skills. Ability to pay attention in detail. Ability to work with a high degree of independence and initiative. Experience with Microsoft Office, Teams, and REDCap.

Special Instructions :

UNC-Chapel Hill and NC State University are collaborating to extend NC State's internal temporary staffing function as a shared service for both institutions. Under this partnership, UTS provides exclusive temporary staffing services to UNC-Chapel Hill and NC State, employing candidates to work as temporary employees in a variety of jobs on both campuses. If interested, please apply here: https://jobs.ncsu.edu/postings/210678



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