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ICON plc
ICON plc
ConsultingHealthcareLogistics
ICON plc is a global contract research organisation serving the healthcare and pharmaceutical industries. Its work spans clinical, consulting, and commercial services that support drug development from early research through post-marketing activities. The company provides solutions including decentralised clinical trials, cardiac safety, early clinical laboratories, medical imaging, regulatory intelligence, and real-world evidence. ICON plc also brings therapeutic expertise to areas such as cardiovascular disease, oncology, internal medicine, cell and gene therapies, and biosimilars, combining data analysis with patient-focused approaches to help advance clinical programmes.
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Clinical Associate at ICON plc - Pennsylvania Remote

Support clinical trial planning, coordination, monitoring, and close-out activities as a Clinical Associate at ICON plc. Contribute to sponsor-dedicated CRO services and the development of innovative treatments.

USUnited StatesPAPennsylvaniaRemoteFull-timeJuniorMiddleEnglish RequiredAssociateGeneral

Description

  • Support the planning, execution, and monitoring of clinical trials while maintaining compliance with protocols, regulations, and industry standards.
  • Coordinate study activities such as site initiation, patient recruitment, data collection, and monitoring visits.
  • Work cross-functionally with Clinical Operations, Data Management, and Biometrics teams.
  • Maintain complete study documentation and records in line with regulations and standard operating procedures.
  • Assist with study close-out, including data cleaning, analysis, and clinical study report preparation.

Requirements

  • Bachelor’s degree in a relevant scientific discipline or healthcare-related field.
  • Prior clinical research or healthcare experience, preferably in the pharmaceutical, biotechnology, or CRO sector.
  • Strong organizational and time-management abilities, including the capacity to prioritize competing tasks effectively.
  • Exceptional attention to detail and problem-solving skills, with a focus on data accuracy, integrity, and compliance.
  • Clear communication and strong interpersonal skills for collaborating across functions and building relationships with study teams and clinical sites.
  • Availability to travel as required.
  • Legal authorization to work in the country where the role is based.

Benefits

  • Competitive base salary with 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.
  • Structured training and career pathways supporting learning and professional development.

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