Clinical Study ICF Writer - US Remote based

Clinical Study ICF Writer - US Remote based

Please ensure you read the below overview and requirements for this employment opportunity completely.

Fortrea is looking for a confident, seasoned Doc Review Senior Specialist who can work independently while collaborating with globally based team members. This individual will provide full and independent review of global project and country regulatory documents. The Doc Review Senior Specialist will respond to CAPAs and may be responsible for mentoring other lower level staff.

Key / Core Responsibilities

• Develop and/or review initial/amended Core Informed Consent Forms (ICFs)
• Review Core/Country/Site Informed Consent Form to assure compliance with sponsor requirements, local regulatory requirements, and Good Clinical Practice (GCP) guidelines
• Review and implementation of relevant study-specific plans that describe the required expectations for assigned tasks.
• Support system compliance and system data entry, as applicable.
• File required task-related documentation in the Electronic Trial Master File (eTMF).
• Liaising and follow-up with local teams, Start-up Project Managers, and Sponsors toassuretimelyapproval of Informed Consent Formsin order tomeet submission deadlines.
• Act as Document Review mentor for lower-level staff and help train lower-level staff on Document Review processes and expectations
• Oversee Local Investigator Package reviewers work for a specific country.
• Serve on SOP Review Team(s) as expert in Document Review processes and expectations.
• Serve as a Subject Matter Expert for partnership processes on Document Review activities such as Informed Consent Form.
• And all other duties as needed or assigned

Required Qualifications:

• University/College degree (life science preferred), or certification in a related allied health profession from an appropriate accredited institution (e.g., nursing certification, medical or laboratory technology).
• Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
• Expert knowledge of ICH, FDA, IRB/IEC, and other applicable regulations/guidelines.
• 5 years work experience in clinical research

Physical Demands / Work Environment:

• Work is performed in an office environment with exposure to electrical office equipment.
• Occasional drives to site locations with occasional travel both domestic and international.
• Frequently stationary for 6-8 hours per day.
• Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
• Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.

Pay Range:USD $90,000-$110,000 / annually

Benefits:All job offers will bebased on a candidates skills and prior relevant experience, applicabledegrees/certifications,as well as internal equity and market data.Regular,full-timeor part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), Paid time off (PTO) or Flexible time off (FTO), Company bonus where applicable.

Application Deadline:June 4, 2026

Learn more about our EEO & Accommodations request here. xywuqvp

Remote working/work at home options are available for this role.