Romania, Bucharest Remote (Global) Full-time

ICON plc is hiring a Senior Clinical Research Associate

About the Role

Senior Clinical Research Associate at ICON plc plays a key role in managing and overseeing clinical trial operations within a sponsor-dedicated team. The position ensures strict adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards throughout the trial lifecycle.

Key Responsibilities:

  • Conduct monitoring activities at clinical trial sites to ensure compliance with protocols, regulations, and GCP.
  • Perform on-site visits, including Site Qualification Visits (SQVs), Site Initiation Visits (SIVs), Interim Monitoring Visits (IMVs), and Close-Out Visits (COVs).
  • Collaborate with cross-functional teams to support accurate and timely data collection and reporting.
  • Train and mentor site staff and other Clinical Research Associates to uphold high-quality trial conduct.
  • Develop and maintain strong relationships with site personnel and stakeholders to ensure efficient trial execution.

Required Qualifications:

  • Advanced degree in life sciences, nursing, medicine, or a related field.
  • Extensive experience as a Senior Clinical Research Associate with in-depth knowledge of clinical trial processes and regulatory standards.
  • Proven ability to manage multiple sites and projects with strong organizational and problem-solving skills.
  • Proficiency in clinical trial software and tools, with a focus on data integrity and site management.
  • Excellent communication and interpersonal abilities, with experience influencing stakeholders in complex environments.
  • Ability to travel at least 60% of the time (domestic and international), including fly and drive.
  • Valid driver’s license is required.

Preferred Qualifications:

  • Prior experience in cardiology clinical trials is advantageous.

Benefits:

ICON offers a comprehensive benefits package including various annual leave entitlements, health insurance options, competitive retirement planning, and access to the Global Employee Assistance Programme (TELUS Health) providing 24/7 support. Additional country-specific benefits may include childcare vouchers, bike purchase schemes, gym memberships, travel subsidies, and health assessments. Life assurance is also provided.

Work Environment:

This role is based in Romania and supports a global team. ICON plc fosters an inclusive, diverse, and sustainable workplace culture that values high performance, talent development, and equal opportunity. The company is committed to providing an accessible, discrimination-free environment and supporting the communities in which it operates.

ICON is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

Required Skills
clinical trial softwareclinical trial processesregulatory requirementssite managementdata integritymonitoring practicesproject managementorganizational skillsproblem-solvingcommunicationinterpersonal skillsstakeholder management clinical trial softwareclinical trial processesregulatory requirementssite managementdata integritymonitoring practicesproject managementorganizational skillsproblem-solvingcommunicationinterpersonal skillsstakeholder management
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About company
ICON plc
ICON plc is a world-leading healthcare intelligence and clinical research organization.
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Posted 23 days ago