Clinical Research Coordinator – Accellacare (Onsite, Salisbury, NC)
Company: ICON plc (Accellacare – ICON Clinical Research Network)
Job Type: Full-Time
Work Model: Onsite (Office Non-Flex)
Location: 410 Mocksville Avenue, Salisbury, North Carolina 28144, United States
Experience Required: Minimum 1+ Year as a Clinical Research Coordinator or Equivalent Role
About ICON plc and Accellacare
ICON plc is a global healthcare intelligence and clinical research organization supporting pharmaceutical, biotechnology, and medical device companies across all phases of clinical development.
This opportunity is with Accellacare, part of ICON’s global clinical research site network, focused on improving patient access, operational efficiency, and high-quality trial delivery. Accellacare integrates site-level excellence with patient-centered research execution to enhance sponsor and participant experiences.
Job Overview
ICON is seeking a Clinical Research Coordinator (CRC) to support onsite clinical trial operations in Salisbury, North Carolina. The CRC will ensure participant safety, regulatory compliance, and protocol adherence while managing study coordination activities across multiple trials.
This role is ideal for early-career to mid-level clinical research professionals seeking hands-on experience in patient recruitment, protocol execution, data management, and site-level regulatory compliance.
Key Responsibilities
Study Start-Up and Recruitment
Execute study start-up activities, including development of recruitment plans and tools.
Conduct phone screenings and identify eligible participants per protocol inclusion and exclusion criteria.
Proactively implement recruitment strategies to meet or exceed enrollment targets.
Maintain accurate recruitment tracking and referral source documentation within the Clinical Trial Management System (CTMS).
Clinical Trial Coordination and Execution
Coordinate and manage multiple clinical trials in accordance with study protocols.
Create and maintain source documents and progress notes per Core Operating Guidelines.
Ensure accurate and timely data entry into Electronic Data Capture (EDC) systems or Case Report Forms (CRFs).
Attend investigator meetings and support sponsor monitoring visits.
Clinical and Technical Procedures
Perform protocol-specific clinical procedures, including:
Phlebotomy and laboratory processing
Blood pressure monitoring
Electrocardiograms (ECG)
Holter monitoring
Pulmonary function testing
Allergy testing
Pregnancy testing and strep screening
Dispense study medication as directed by the Investigator.
Participant Safety and Compliance
Continuously review participant eligibility throughout the study lifecycle.
Document laboratory data and adverse events accurately.
Promptly notify Investigators, Institutional Review Boards (IRB), and sponsors of serious adverse events.
Maintain adherence to Good Clinical Practice (GCP) and regulatory standards.
Collaboration and Quality Assurance
Build strong working relationships with Investigators and site leadership.
Maintain regular communication with sponsor monitors.
Support mentoring initiatives and assist with site-level quality assurance activities.
Required Qualifications and Experience
Bachelor’s Degree in Life Sciences, Healthcare, Nursing, Public Health, or related field.
Minimum 1+ year of experience as a Clinical Research Coordinator or equivalent clinical research role.
Strong knowledge of clinical trial processes and GCP guidelines.
Experience with CTMS and Electronic Data Capture (EDC) systems preferred.
High attention to detail and strong organizational skills.
Ability to manage multiple studies and priorities effectively.
Strong written and verbal communication skills.
Demonstrated interest in advancing a career in clinical research.
Preferred Skills
Experience performing clinical procedures within research settings.
Familiarity with regulatory reporting requirements and IRB processes.
Ability to work independently while collaborating within a site-based team.
Compensation and Benefits
ICON offers competitive compensation and comprehensive benefits tailored to support employee well-being and work-life balance. Benefits may include:
Health insurance options
Retirement savings plans
Paid annual leave
Life assurance
Employee Assistance Programs
Flexible voluntary benefits
ICON is committed to diversity, inclusion, and equal employment opportunity. All qualified applicants will receive consideration without discrimination.
Who Should Apply?
This role is ideal for:
Clinical Research Coordinators
Site-Level Clinical Trial Professionals
Healthcare Professionals Transitioning into Clinical Research
Early-Career Clinical Operations Specialists
If you have hands-on experience coordinating clinical trials and are seeking to grow within a global clinical research network, this onsite opportunity in Salisbury, NC offers strong professional development potential.
For more global clinical research, regulatory affairs, site operations, and life sciences career opportunities, visit ThePharmaDaily.com.
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