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CRA II or Senior CRA

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ICON plc

9d ago

  • Job
    Full-time
    Mid & Senior Level
  • Research & Development
    Healthcare
  • Madrid
  • Quick Apply

AI generated summary

  • You should have an advanced degree in life sciences, extensive CRA experience, strong organizational skills, monitoring expertise, and excellent communication abilities to manage sites and projects effectively.
  • You will monitor trial sites, conduct visits for performance assessments, support data collection, train site staff, and build relationships to ensure successful clinical trial execution.

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.

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.

FAQs

What is the job title associated with this position?

The job title is Senior Clinical Research Associate (CRA) or CRA II.

What organization is offering this position?

This position is offered by ICON plc, a healthcare intelligence and clinical research organization.

What are the primary responsibilities of a Senior CRA at ICON?

The primary responsibilities include monitoring clinical trial sites, conducting site visits, collaborating with cross-functional teams, providing training and guidance to site staff, and maintaining effective relationships with site personnel and stakeholders.

What qualifications are required for this position?

Candidates should have an advanced degree in a relevant field, extensive experience as a Clinical Research Associate, strong organizational and problem-solving skills, expertise in monitoring practices and data integrity, and excellent communication skills.

Does ICON offer benefits for this position?

Yes, ICON offers a range of additional benefits, including various annual leave entitlements, health insurance options, retirement planning offerings, and a global Employee Assistance Programme.

Is diversity and inclusion emphasized in the workplace at ICON?

Yes, ICON places a strong emphasis on diversity, inclusion, and belonging as fundamental values of its culture.

How does ICON support employees with medical conditions or disabilities during the application process?

ICON is committed to providing reasonable accommodations for candidates with medical conditions or disabilities as needed for the application process or to perform essential job functions.

Can I apply for this position even if I don't meet all the requirements?

Yes, candidates are encouraged to apply regardless of whether they meet all the requirements, as there’s a chance they may still be what ICON is looking for.

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ICON plc

Science & Healthcare
Industry
10,001+
Employees

Mission & Purpose

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.