Senior Medical Writer – Phase I-IV (Global)

Worldwide Clinical Trials; Durham (NC); On-site; USD 67,000 - 132,000; Full time

Job summary

Worldwide Clinical Trials seeks a Late Phase Medical Writer II to perform medical writing for Phase I–IV studies across USA, Europe and ROW. You will prepare protocols, ICFs, CTRs and related documents in alignment with Sponsor specifications and regulatory requirements.

The role requires strong English, excellent writing and project management skills, and willingness to travel domestically and internationally to support global studies with our team of 3,500+ experts.

Qualifications

• University/college degree in life science or related field or equivalent experience.
• Minimum of 3 years of medical writing experience.
• Willingness to travel domestically and internationally (passport required).

Responsibilities

• Lead medical writing on Phase I–IV studies in USA, Europe and ROW.
• Prepare and lead documents such as protocols, ICFs, CTRs and NDA/CTD components.
• Coordinate internal and Sponsor reviews and ensure regulatory compliance.
• Review and QC documents as needed.

Skills

Excellent written English

Project/time management

Microsoft Office

Clear written communication

Independent work

Deadline-driven

Education

Life science degree

Tools

Word

PowerPoint

Excel

Outlook

Job description

Worldwide Clinical Trials seeks a Late Phase Medical Writer II to perform medical writing for Phase I–IV studies across USA, Europe and ROW. You will prepare protocols, ICFs, CTRs and related documents in alignment with Sponsor specifications and regulatory requirements.

The role requires strong English, excellent writing and project management skills, and willingness to travel domestically and internationally to support global studies with our team of 3,500+ experts.