Informed Consent Writer

Job Summary

Working remotely, the Informed Consent Writer will develop, review, and revise informed consent documents for clinical trials, ensuring compliance with regulatory standards.

Key responsibilities

• Draft and edit informed consent forms in accordance with regulatory guidelines
• Collaborate with clinical teams to ensure clarity and accuracy in consent documents
• Review and incorporate feedback from stakeholders to enhance document quality

Required qualifications

• Bachelor's degree in a relevant field, such as life sciences or medical writing
• Experience in medical writing or regulatory submissions
• Familiarity with clinical trial processes and regulatory requirements
• Strong understanding of ethical considerations in informed consent
• Ability to work independently and manage multiple projects simultaneously