Jobs · Analyst

Senior CRA

ICON Strategic Solutions · Washington, DC · 1 mo ago
RemoteRemoteAnalystFull-time

About the role

ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

Responsibilities

  • 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.

Requirements

  • 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.

Qualifications

  • Must be located in the Midwest (Illinois, Indiana, Iowa, Kansas, Michigan, Minnesota, Missouri, Nebraska, North Dakota, Ohio, South Dakota, and Wisconsin).
  • Oncology monitoring experience is required.
  • Ability to travel at least 60% of the time (international and domestic - fly and drive), and should possess a valid driver's license.

Skills

  • Strong knowledge of clinical trial processes and regulatory requirements.
  • Proficiency in monitoring practices, data integrity, and site management.
  • Effective communication and interpersonal skills.
  • Ability to manage multiple projects and sites simultaneously.

Benefits

  • Variety of annual leave entitlements.
  • A range of health insurance offerings to suit your and your family’s needs.
  • Competitive retirement planning offerings to maximize savings and plan for the future.
  • Global Employee Assistance Program (LifeWorks) offering 24-hour access to a global network of over 80,000 independent specialized professionals.
  • Life assurance.
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Pay

TBD

Schedule

Remote

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