Clinical Research Coordinator

Overview

Clinical Research Coordinator at Accellacare, part of ICON's clinical research network. This role supports transforming the clinical trial experience for patients and sponsors by delivering better access, greater efficiency, and improved outcomes in clinical research.

410 Mocksville Avenue, Salisbury, North Carolina 28144 USA

The CRC ensures participant safety, promotes the mission of Accellacare, and works with supervision to meet and exceed priorities. The CRC actively recruits and promotes Accellacare services to suitable participants and sponsor representatives. The CRC I will autonomously perform tasks required to coordinate and complete multiple studies according to the protocol, and assist the Manager of Clinical Operations and Sr. Clinical Research Coordinators with staff development through mentoring and site-level quality assurance.

• Performs study start-up duties including production of recruitment tools and progress notes, and screens patients on site to identify trial participants
• Develops and executes recruitment plans to meet enrollment goals
• Completes training on the Clinical Trial Management System and maintains skills to update the database, process participant reimbursements, capture referral sources, and create call lists to promote recruitment
• Attends investigator meetings
• Creates and updates source documents and progress notes using templates in the Core Operating Guidelines
• Accurately collects study data via source documents and progress notes as required by the protocol
• Performs technical protocol-related tasks (e.g., lab work, vital signs, ECGs, monitoring, pulmonary function testing, various eligibility testing) as ordered by the investigator or protocol
• Performs ongoing reviews of inclusion and exclusion criteria for participants and conducts peer review of criteria for trials
• Documents laboratory data and adverse reactions, presents information to investigators promptly, and notifies investigators, the Institutional Review Board, and sponsor of serious adverse events
• Builds and maintains strong relationships with investigators and communicates trial status and participant information
• Dispenses study medication under the direction of the Investigator
• Maintains communication with the monitor from the sponsoring company via telephone, written communication, and on-site visits
• Enters visit data in the Electronic Data Capture (EDC) or Case Report Forms (CRF) within sponsor timelines

• Bachelor's Degree
• 1+ years of experience as a clinical research coordinator or equivalent
• High attention to detail
• Interest in a clinical research career

Our success depends on the quality of our people. We prioritize a diverse culture that rewards high performance and nurtures talent. In addition to a competitive salary, ICON offers a range of benefits designed to be competitive within each country and focused on well-being and work-life balance for you and your family.

• Various annual leave entitlements
• Health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings
• Global Employee Assistance Programme, Life Works, offering 24-hour access to a global network of professionals
• Life assurance
• Flexible country-specific optional benefits (e.g., childcare vouchers, bike purchase schemes, gym memberships, subsidized travel passes, health assessments)

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion and belonging are fundamental to our culture and values. We are committed to an inclusive and accessible environment for all candidates and to equal employment opportunities regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. If you need a reasonable accommodation for any part of the application process or to perform essential functions of a position, please let us know.

Interested in the role but unsure if you meet all the requirements? We encourage you to apply regardless—there’s every chance you’re exactly what we’re looking for at ICON, whether for this role or others.

Are you a current ICON employee? Please  to apply.