Clinical Research Expert

5 days ago


Burlington, Ontario, Canada ICON Full time

Unlock your potential in clinical research with a rewarding career at ICON

About the Role

We're seeking an experienced Clinical Research Expert to join our team as an Informed Consent Form Specialist. As a key member of our study start-up team, you'll play a crucial role in reviewing and negotiating informed consent forms to ensure compliance with regulatory requirements.

Your main responsibilities will include:

  • Reviewing and revising informed consent forms to ensure accuracy and compliance
  • Negotiating language changes with sponsors and stakeholders
  • Assisting in the drafting of ICF country templates for the United States and Canada
Requirements

To be successful in this role, you'll need:

  • A bachelor's degree in life sciences, nursing, or pharmaceuticals
  • 3 years of experience in clinical research, preferably in a CRO, pharmaceutical company, or study site
  • Excellent communication skills, attention to detail, and proficiency in computer software
About Us

At ICON, we're committed to fostering a diverse and inclusive work environment that values innovation, excellence, and teamwork. Our employees are the driving force behind our success, and we offer a range of benefits and opportunities for growth and development.

What We Offer

In addition to a competitive salary, you can expect:

  • $85,000 - $110,000 per year (dependent on location and experience)
  • A comprehensive benefits package, including health insurance, retirement plans, and paid time off
  • Opportunities for professional growth and development through training and mentorship
Why Choose ICON?

As a leader in clinical research, ICON offers a dynamic and challenging work environment that allows you to make a real difference in people's lives. With a focus on diversity, inclusion, and belonging, we're proud to foster a culture that values collaboration, creativity, and innovation.



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