Senior Clinical Research Coordinator – Oncology

ICON plc

Senior Oncology Clinical Research Coordinator conducting onsite trials for ICON, a global healthcare intelligence and clinical research organisation. Managing recruitment, protocol procedures, patient safety, and site coordination.

Posted 8/12/2026full-timeLisle • Illinois • 🇺🇸 United StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial management, including recruitment strategies, patient education, and adherence to GCP standards. Proficient in clinical procedures and capable of training staff while maintaining strong relationships with investigators and sponsors.

Highest-signal resume keywords

Oncology Clinical Research ExperienceClinical Research Coordinator ExperiencePhlebotomy SkillsGCP KnowledgeTime Management Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementPatient RecruitmentProtocol-Specific ProceduresDatabase ManagementAdverse Event ReportingInformed Consent ProcessLaboratory Data DocumentationStudy Medication DispensingScreening Criteria ReviewLogistical Planning

Soft Skills

Organizational SkillsCommunication SkillsRelationship BuildingTraining and DevelopmentTeam Collaboration

Tools & Technologies

Clinical Trial Management System

Industry Keywords

Clinical TrialsLife SciencesHealthcarePatient EducationInvestigator MeetingsSite EvaluationRetention StrategiesRecruitment PlansSite Documentation RequirementsAccellacare Site Network

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Perform study start-up duties, including recruitment plans, recruitment tools, progress notes, and phone screening
Plan logistical needs for clinical trials and assist CRC Level I and Level II staff with trial planning and conduct
Evaluate recruitment needs, communicate recruitment efforts, and execute plans to generate randomized patients and maximize retention
Attend investigator meetings
Maintain Clinical Trial Management System skills and update databases, reimburse participants, capture referral sources, and create recruitment call lists
Perform protocol-specific clinical procedures and train others on technical requirements
Review patient inclusion and exclusion criteria during screening
Document laboratory data and adverse reactions and notify investigators, the Institutional Review Board, and sponsors of serious adverse events
Dispense study medication at the Investigator’s direction
Establish relationships with patient volunteers, provide patient education, and conduct informed consent
Communicate patient, recruitment, and clinical status to investigators and sponsoring-company monitors
Maintain relationships with monitors and sponsors and promote the site for future trials
Prospect for new business and develop physician relationships
Monitor and review other coordinators and support staff
Attend site evaluation visits as a senior staff representative
Assist with training and development of site personnel
Travel to other Duly sites within the Accellacare Site Network

Requirements

What you’ll need

Oncology clinical research industry experience
3+ years of experience as a Clinical Research Coordinator
Clinical skills, such as phlebotomy
Good understanding of clinical trial processes, GCP, and site documentation requirements
Excellent time management and planning skills with an organized approach to work
Bachelor’s degree in life sciences, healthcare, or a related field
Legal right to work in the country where the role is based

Benefits

Comp & perks

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways
Reasonable accommodations during the recruitment process
Inclusive and accessible workplace