Senior Medical Writer
hace 2 días
Job Summary
As a Senior Medical Writer at Syneos Health, Inc., you will be responsible for mentoring and leading less experienced medical writers on complex projects. You will represent the Medical Writing department on clinical study teams, at conferences, and for presentations to clients regarding writing projects. Your expertise will be sought after to advise clients and study teams on data presentation and production strategies, ensuring that client objectives and quality standards are met. You will develop good working relationships with internal and external colleagues and manage medical writing activities associated with individual studies, coordinating activities within and across departments with minimal supervision. Your responsibilities will include developing a variety of documents, such as clinical study protocols, clinical study reports, patient narratives, and clinical development plans. You will also review statistical analysis plans and table/figure/listing specifications for appropriate content, grammar, format, and consistency. If you are a skilled medical writer with excellent leadership and communication skills, we encourage you to apply for this challenging and rewarding role.
About the Role
This is a key leadership position within the Medical Writing department, and you will be responsible for driving the development of high-quality clinical content. You will work closely with cross-functional teams, including clinical operations, biostatistics, and regulatory affairs, to ensure that clinical study reports and other documents meet the highest standards of quality and accuracy. Your expertise will be essential in advising clients and study teams on data presentation and production strategies, and you will be responsible for mentoring and leading less experienced medical writers on complex projects. If you are a motivated and experienced medical writer with excellent leadership and communication skills, we encourage you to apply for this challenging and rewarding role.
Responsibilities
• Mentors and leads less experienced medical writers on complex projects
• Represents the Medical Writing department on clinical study teams, at conferences, and for presentations to clients regarding writing projects
• Advises clients and study teams on data presentation and production strategies
• Develops good working relationships with internal and external colleagues
• Manages medical writing activities associated with individual studies, coordinating activities within and across departments with minimal supervision
• Develops a variety of documents, such as clinical study protocols, clinical study reports, patient narratives, and clinical development plans
• Reviews statistical analysis plans and table/figure/listing specifications for appropriate content, grammar, format, and consistency
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