Senior Medical Writer — Remote, Cross-Functional Lead

Synterex, Inc.; New Jersey; Hybrid; USD 80,000 - 110,000; Full time

Job summary

Synterex, Inc. is seeking a Senior Medical Writer to join their team remotely. This role involves leading the planning and preparation of clinical regulatory documents while collaborating with various departments. The ideal candidate has over 5 years of experience in medical writing within the CRO/biotech industry.

This position requires excellent project management skills, familiarity with regulatory requirements, and proficiency in Microsoft Word. Interested applicants should reach out via [e-mail].

Qualifications

• 5+ years of experience as a medical writer in the CRO/biotech/pharmaceutical field.
• Familiarity with ICH and US regulatory requirements.
• Experience writing clinical study reports and protocols.

Responsibilities

• Lead the execution of documents and manage timelines.
• Coordinate client contributors and internal resources for timely document completion.
• Ensure adherence to client processes and templates.

Skills

Medical writing

Project management

Regulatory documentation

Conflict management

Strong communication

Education

Bachelor's degree or higher in a relevant field

Tools

Microsoft Word

Document management systems

Job description

Synterex, Inc. is seeking a Senior Medical Writer to join their team remotely. This role involves leading the planning and preparation of clinical regulatory documents while collaborating with various departments. The ideal candidate has over 5 years of experience in medical writing within the CRO/biotech industry.

This position requires excellent project management skills, familiarity with regulatory requirements, and proficiency in Microsoft Word. Interested applicants should reach out via [e-mail].