Clinical Research Regulatory Medical Writer
Clinical Research Regulatory Medical Writer
Connect Life Sciences
Canton, MI
See who Connect Life Sciences has hired for this role
Medical Writing Opportunity with Clinical Research Organization
Responsibilities
Employment Type: Full-Time
Responsibilities
- Critically evaluate, analyze, and interpret medical literature for study design, statistical significance, scientific rigor, and bias absence
- Write and edit various clinical development documents such as clinical protocols, reports, consent forms, and presentation materials
- Meet deadlines, adapt to changes, and maintain workflow for writing assignments
- Provide excellent customer service internally and externally
- Communicate effectively with clients and project team members
- Proactively seek guidance and information from colleagues when needed
- Minimum of 3 years of industry or pharma postdoctoral experience
- Masters or Ph.D. in a scientific, medical, or clinical discipline preferred
- Strong understanding of scientific data
- Exceptional writing skills
- Excellent organizational and multitasking abilities
- Proficiency in MS Word, Excel, PowerPoint, and other word processing tools
- Regulatory writing experience and familiarity with client templates and style guides a bonus
- Knowledge of federal regulations, Good Clinical Practices, and ICH guidelines advantageous
Employment Type: Full-Time
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Seniority level
Mid-Senior level -
Employment type
Full-time -
Job function
Marketing, Public Relations, and Writing/Editing -
Industries
Staffing and Recruiting
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