Remote Medical Writing Consultant I — Regulatory Docs

Syner-G; United States; Remote; USD 80,000 - 120,000; Full time

Benefits offered by this job

Flexible paid time off

Company-paid holidays

Annual incentive plan

Career development opportunities

Job summary

Syner-G is seeking a qualified professional to focus on regulatory documentation for clinical studies. The role involves authoring clinical study reports, developing regulatory strategies, and collaborating with cross-functional teams to ensure compliance.

The ideal candidate will possess an advanced degree in a life or health science and have substantial experience in regulatory submissions. This position offers flexibility with remote work options and a market-competitive salary.

Qualifications

• 3+ years of experience in the industry related to regulatory submissions.
• Proficiency in document management and regulatory standards.
• Strong writing and communication skills in scientific context.

Responsibilities

• Author regulatory documents including clinical study reports.
• Lead the development of complex regulatory documents.
• Coordinate timelines and client interactions.

Skills

Medical writing

Regulatory writing

Project management

Data analysis

Communication skills

Education

Advanced degree in life or health science

RAC certification

Tools

Microsoft Office Suite

Veeva Vault

MS Project

Job description

Syner-G is seeking a qualified professional to focus on regulatory documentation for clinical studies. The role involves authoring clinical study reports, developing regulatory strategies, and collaborating with cross-functional teams to ensure compliance.

The ideal candidate will possess an advanced degree in a life or health science and have substantial experience in regulatory submissions. This position offers flexibility with remote work options and a market-competitive salary.