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ICON plc

Patient Recruitment Associate

ICON plc

Patient Recruitment Associate supporting clinical research participation through patient engagement and database management. Collaborating with healthcare teams to enhance trial recruitment efforts.

Posted 7/29/2026contractWinston-Salem • North Carolina • 🇺🇸 United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical research processes, patient recruitment, and effective communication to enhance participant engagement and ensure high-quality data management. Proficient in utilizing clinical trial management software and Microsoft Office Suite to maintain accurate records and support operational efficiency.

Highest-signal resume keywords
Clinical Research Site ExperiencePatient RecruitmentExcellent Communication SkillsOrganizational SkillsCustomer Service Experience

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Trial Management SoftwareMedical TerminologyData EntryPatient SchedulingMultitasking Under Pressure
Soft Skills
Interpersonal SkillsProblem SolvingAttention to DetailBuilding RapportFollow-Up Skills
Tools & Technologies
Microsoft Office SuiteExcelWordOutlook
Industry Keywords
Life ScienceHealthcareClinical ResearchPatient ExperienceEnrollment Optimization

About the role

Key responsibilities & impact
  • Screen potential study participants accordingly to protocol inclusion and exclusion criteria by asking study specific questions
  • Review, enter, and edit patient information into clinical trial management software
  • Book patients into site schedulers ensuring that entries are accurate and up to date
  • Read and understand the purpose and inclusion/exclusion criteria for each protocol
  • Respond to all leads within a 24-hour time period
  • Identify appropriate study opportunities for interested volunteers based on knowledge of clinical trials and neighboring locations
  • Problem solve and create contingency plans to optimize enrollment
  • Effectively communicate the importance of research participation to volunteers
  • Provide an exceptional patient experience by building positive rapport and consistent follow-up
  • Strive to meet personal and team targets
  • Work in strict confidentiality in all forms including electronically, written forms, and verbal
  • Remain accountable for delivering high quality, accurate work, ensuring all administration is filed accordingly

Requirements

What you’ll need
  • Bachelors degree in life science, healthcare, or medical field
  • Clinical research site experience (strongly preferred) with an interest in a career clinical research, preferably in patient recruitment
  • Experience in customer service, marketing, and/or sales (preferred)
  • Basic understanding of medical terminology
  • Excellent communication and interpersonal skills with comfortability fielding inbound and outbound phone calls
  • Ability to multitask while working under pressure and with tight deadlines
  • Organizational skills with attention to detail
  • Computer skills, specifically with Microsoft Office Suite (Excel, Word, Outlook)
  • Ability to work onsite in either Statesville, NC or Winston-Salem, NC 4 days per week

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