Clinical Research Coordinator - Accellacare

Clinical Research Coordinator

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

This role is with Accellacare, part of ICON's clinical research network, where you’ll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site network is designed with one goal in mind: to deliver better access, greater efficiency, and improved outcomes in clinical research.

Title: Clinical Research Coordinator

Location: 410 Mocksville Avenue, Salisbury, North Carolina 28144 USA

Summary: The CRC ensures the safety of our participants, promotes the mission of Accellacare, and consistently strides to meet and exceed priorities discussed with supervisor. The CRC will actively recruit and promote our service to suitable participants and sponsor representatives. Additionally, the CRC will autonomously perform tasks required to coordinate and complete multiple studies according to the protocol. Lastly, they will assist the Manager of Clinical Operations and Sr.

Clinical Research Coordinators with staff development through mentoring and site level quality assurance.

• Perform study start-up duties including the production of a recruitment tool and progress notes, as well as phone screening patients and identifying participants for trials on site.
• Proactively develop and execute recruitment plans that meet and exceed enrollment goals.
• Complete training on Clinical Trial Management System and maintain proper skills to update the database, complete participant reimbursement, capture referral source of participants, and create call lists to promote recruitment.
• Attend investigator meetings.
• Create and update source documents/progress notes and utilize templates provided in the Core Operating Guidelines.
• Accurately collect study data via source documents/progress notes as required by the protocol.
• Perform technical requirements of the study protocol, e.g., lab work (phlebotomy and processing), blood pressure, electrocardiograms, Holter monitoring, pulmonary function testing, allergy testing, urine/serum pregnancy testing, strep throat screening, or any procedure necessary for the protocol as ordered by the investigator or specified by a protocol.
• Perform continuous reviews of the inclusion and exclusion criteria for each participant during the trial for your trials as well as peer review of inclusion and exclusion for trials.
• Document laboratory data and adverse reactions, present this information to an investigator in a timely manner, and immediately notify investigators, the Institutional Review Board and sponsor of any serious adverse events.
• Build and maintain strong relationships with Investigators and provide ongoing communication about trial status and participants.
• Dispense study medication at the direction of the Investigator.
• Maintain communication with the monitor from the sponsoring company through telephone contact, written communication and on‑site visits.
• Enter visit data in the Electronic Data Capture (EDC) or Case Report Forms (CRF) within timelines provided by sponsor.

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

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well‑being and work‑life balance opportunities for you and your family.

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, Life Works, offering 24‑hour access to a global network of over 80,000…