boutique Vendor Benefits

Our founders have over 60 combined years of full-time writing experience and MW management within pharma/biotech companies. We also have a group of consulting writers who we have worked with for over 15 years. Together we: 

• Work independently and directly with multi-functional project teams to successfully deliver high-quality documents on time
• Understand and quickly respond to the often changing priorities within companies and project teams
• Advise teams on best practices for writing & reviewing documents and how to optimize the process 

Our team at SRSC has a  broad background in the biomedical sciences and extensive experience in:

• Scientific research, including an advanced knowledge of experimental design and statistical analysis
• Ability to work successfully on complex projects/documents
• Co-authoring documents with other scientists/clinicians
• Project management and team leadership, with an ability to prospectively identify programmatic and scientific/clinical issues 

We are dedicated to optimizing clinical drug development and time to patient access through highly effective, targeted communication by:

• Consolidating, synthesizing, analyzing, and generating new information based on data, existing literature, input from external experts, and the expertise of all team members
• Ensuring that the collection, interpretation, and communication of study data for any given project support the filing plan and the business needs
• Ensuring that all data and key messages are effectively and consistently communicated within and across documents to a wide range of audiences over the course of a product’s lifecycle