Senior Clinical Research Coordinator

UNC-Chapel Hill • Chapel Hill, NC

6h

About The Position

This position will serve as a Senior Clinical Research Coordinator within the Institute for Trauma Recovery. 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. 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 mentor and subject matter expert. The primary purpose of this position is to support the Principal Investigators (PIs) and Institute Manager on several current and pending research projects. This position will be responsible for a broad range of duties related to planning, organizing, executing, and monitoring the implementation of new and existing clinical trials and other research initiatives. Duties will include supporting the PI with maintaining research methods, tracking patients in the study, provide feedback and suggestion on the development/revision of research protocols and regulatory correspondence as well as maintaining accurate and updated manuals of procedures for the studies. This position will serve as senior coordinator on one or more of the ongoing clinical trials in the institute. In addition to the above, this position will assist with study design, and the development of study procedures, budget management, and regulatory oversight. This position will be responsible for supervising research staff and student volunteers.

Requirements

• 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.
• 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 problem solving skills.

Nice To Haves

• Not applicable.

Responsibilities

• Planning, organization, conduct, and evaluation of multi-faceted clinical research protocols
• Study execution
• Developing strategies and solutions to improve study processes and execution
• Providing reviews of other team members’ work product
• Serving as mentor and subject matter expert
• Supporting the PI with maintaining research methods
• Tracking patients in the study
• Provide feedback and suggestion on the development/revision of research protocols and regulatory correspondence
• Maintaining accurate and updated manuals of procedures for the studies
• Assisting with study design
• Development of study procedures
• Budget management
• Regulatory oversight
• Supervising research staff and student volunteers

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: No Education Listed
• Number of Employees: 11-50 employees