myGwork - LGBTQ+ Business Community

myGwork - LGBTQ+ Business Community

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21 días
Expira 05/08/2025

Senior CRA

Senior CRA

About the Role

Join ICON plc, a leading clinical research organization, and partner with global pharmaceutical clients to advance groundbreaking medicines and therapies. As a Clinical Research Associate, you will have the opportunity to monitor clinical trials, ensuring compliance and data integrity.

Responsibilities

  • Conduct onsite and remote monitoring in line with ICH-GCP guidelines.
  • Confirm informed consent procedures are rigorously followed.
  • Ensure clinical data integrity and regulatory compliance.
  • Prepare and submit reports on investigational site findings.
  • Assist in audit preparations and provide training to new team members.

Candidate Profile

  • Bachelor’s in health or life sciences.
  • 4+ years of clinical trial monitoring experience.
  • Oncology experience is a plus.
  • Fluent in English and the local language.

Benefits at ICON

ICON values its employees and offers a competitive salary along with various benefits focused on well-being and work-life balance. For more details, visit our careers website.

Commitment to Inclusion

At ICON, we prioritize diversity and inclusion. We encourage all qualified applicants to apply without regard to race, color, religion, gender identity, or disability. For accommodation inquiries during the application process, visit here.

Apply Today

Even if you're unsure about your qualifications, we encourage you to apply. You may be the perfect fit for our team at ICON.