Medical Writing Opportunity with Clinical Research Organization
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
Requirements
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
If you have a background in medical writing and are looking for a challenging opportunity with a reputable Clinical Research organization, we encourage you to apply for this position.
Employment Type: Full-Time
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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