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Clinical Research Coordinator - Accellacare

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ICON
1+ years
Not Disclosed
United States
10 Feb. 25, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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.