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Sr. Clinical Research Associate
Sr. Clinical Research AssociateICON Strategic Solutions • Burlington, Halton Region, CA
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Sr. Clinical Research Associate

Sr. Clinical Research Associate

ICON Strategic Solutions • Burlington, Halton Region, CA
30+ days ago
Job type
  • Full-time
Job description

Senior Clinical Research Associate

Overview

ICON plc is a world‑leading healthcare intelligence and clinical research organization. We foster an inclusive environment that drives innovation and excellence, and we welcome you to join our mission to shape the future of clinical development.

We are currently seeking a Senior Clinical Research Associate (CRA) to oversee and manage clinical trial activities, ensuring they are conducted according to protocol, regulatory requirements, and industry standards. The Senior CRA contributes to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.

What You Will Be Doing

  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
  • Collaborating with cross‑functional teams to ensure timely and accurate data collection and reporting.
  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile

  • Advanced degree in a relevant field such as life sciences, nursing, or medicine.
  • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
  • Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem‑solving skills.
  • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
  • Ability to travel at least 60% of the time (international and domestic) and possession of a valid driver’s license.
  • What ICON Can Offer You

    In addition to a competitive salary, ICON offers a range of benefits designed to support well‑being and work‑life balance for you and your family. Our benefits are competitive within each country.

    Our Benefits Examples Include

  • Various annual leave entitlements.
  • Health insurance offerings to suit you and your family’s needs.
  • Competitive retirement planning offerings.
  • Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a global network of professionals who support well‑being.
  • Life assurance.
  • Flexible country‑specific optional benefits such as childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, and others.
  • Seniority level

    Mid‑Senior level

    Employment type

    Full‑time

    Job function

    Research, Analyst, and Information Technology

    Industries

    Pharmaceutical Manufacturing

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    Sr Clinical Research Associate • Burlington, Halton Region, CA

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