Opportunity with Clinical Research Organization for Regulatory Medical Writers
Are you a skilled medical writer looking to make an impact in the Clinical Research field? Join Connect Life Sciences' partnered Clinical Research organization as a Regulatory Medical Writer and contribute to essential document preparation for clinical development.
Responsibilities

• Evaluate and analyze medical literature to select appropriate resources for study design and scientific integrity
• Draft and revise various clinical development documents, including protocols and clinical study reports
• Maintain project timelines and adapt to changing scopes or deadlines
• Provide excellent customer service and communication with internal and external stakeholders
• Collaborate closely with clients and internal teams to ensure project success

Key Requirements

• Minimum 3 years of experience in the industry or pharmaceuticals
• A Master's or Ph.D. in a scientific or clinical discipline is preferred
• Strong understanding of scientific data and exceptional writing skills
• Proficiency in MS Word, Excel, PowerPoint, and similar word processing tools
• Regulatory writing experience and familiarity with client templates a bonus
• Knowledge of federal regulations, Good Clinical Practices, and ICH guidelines advantageous

If you are a detail-oriented professional with a passion for medical writing and regulatory compliance, we encourage you to apply and take your career to the next level with us.
Employment Type: Full-Time