Clinical Trial Coordinator

ICON plc

Blue Bell, SDRemote OKFull time
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Location
Blue Bell, SD
Work style
Remote OK
Job type
Full time
Posted
Oct 22
3 days ago
Career path

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About the company

ICON plc

Biotechnology Research · 10,001+ employees

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times.

We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.

ICON plc on LinkedIn

What you'll do

  • The Clinical Trial Coordinator supports clinical trial site management by assisting with monitoring activities and ensuring strict adherence to study protocols and regulatory guidelines.
  • They also collaborate with cross-functional teams to maintain accurate documentation and track site performance metrics.

What you need

  • Candidates must hold a bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research.
  • Strong organizational skills, attention to detail, and the ability to work collaboratively in a team environment are essential for this role.
  • Education: a bachelor's degree

Key skills

Clinical researchSite managementSite monitoringProtocol complianceRegulatory requirementsGood Clinical PracticeGCPDocumentation preparationData entryPerformance metricsCommunicationInterpersonal skillsOrganizational skillsAttention to detailClinical trial management

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Perks

  • Competitive base salary
  • Performance related incentives
  • Medical coverage
  • Dental coverage
  • Vision coverage
  • Retirement plans
  • Pension plans
  • Life assurance
  • Disability coverage
  • Employee assistance programmes
  • Wellbeing resources
  • Learning and development opportunities

See full description on company page, apply now

Read the full posting here
Clinical Trial Coordinator At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a SMA I at ICON, you will support the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols, and maintain high standards of operational efficiency. What You Will Do: Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders. Key responsibilities include: Assisting in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Supporting site management activities, including documentation preparation, data entry, and tracking site performance metrics. Collaborating with cross-functional teams to facilitate communication and address site-related issues effectively. Maintaining accurate records of site activities and contributing to the preparation of monitoring reports. Participating in training and development initiatives to enhance knowledge and skills in clinical trial management. Your Profile: You will bring relevant clinical research experience, along with the following qualifications and skills. Required qualifications and experience: Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research. Some experience in clinical research, site management, or related administrative roles is preferred but not mandatory. Strong organizational skills and attention to detail, with the ability to manage multiple tasks effectively. Basic knowledge of clinical trial processes and regulatory requirements is a plus. Excellent communication and interpersonal skills, with the ability to work collaboratively within a team environment. Willingness to travel as required (approximately 25%) Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: 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 Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here. Are you a current ICON Employee? Please click here to apply

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