Senior Study Start Up Associate

4 days ago

Burlington, Ontario, Canada ICON Full time

Senior Study Start Up Associate - Canada

ICON plc is a world-leading healthcare intelligence and clinical research organization.

As a Study Start Up Associate - Informed Consent Form Reviewer, your main role is to review and negotiate language in Informed Consent Forms.

You will assist in drafting ICF country templates for the United States and Canada, which are then distributed to study sites to make edits depending on their local IRB requirements and SOPs.

Additionally, you will review and negotiate changes to the ICF and potentially liaise with other stakeholders like the sponsor, legal, or the clinical team to ensure that changes are acceptable.

  1. A bachelor's degree in the life sciences, nursing, and/or pharmaceuticals is preferred or equivalent.
  2. Three years of experience in clinical research in a healthcare or research setting at either a CRO, pharmaceutical company, study site, or who have worked at an IRB.
  3. Experience must include performing ICF review as an essential function of the job.
  4. Excellent oral and written communication skills in English, strong attention to detail, and proficient computer skills are required.

Benefits of Working in ICON

Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.

We offer a range of health-related benefits to employees and their families, including competitive retirement plans, life assurance, and more.

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