Clinical Research Writer

About The Role:

The Clinical Research Writer will be responsible for building and leading a structured clinical research and outcomes function. This role will organize research efforts across programs, analyze clinical and operational data, and lead the development of abstracts, manuscripts, and peer-reviewed cardiovascular (CV) publications.

Research Strategy & Organization:

• Develop and maintain a structured research roadmap aligned with organizational clinical priorities
• Organize research initiatives across multiple clinical programs and stakeholders
• Establish standardized processes for study design, data requests, analysis, and publication timelines
• Coordinate cross-functional collaboration with clinical, data, product, and operations teams

Data Analysis & Evidence Generation:

• Analyze large clinical and administrative datasets (e.g., EHR, monitoring data, claims when available)
• Conduct outcomes, quality, and utilization analyses using appropriate statistical methods
• Partner with data teams to define data requirements and ensure data quality and integrity
• Translate analyses into clinically meaningful insights and conclusions

Publications & Abstract Development:

• Lead authorship and coordination of abstracts, posters, and manuscripts for CV conferences and journals
• Draft and revise manuscripts in collaboration with clinical leaders and co-authors
• Manage submission processes for conferences and peer-reviewed journals
• Support responses to reviewer comments and revisions

Governance, Compliance & IRB:

• Support IRB submissions, exemptions, and regulatory documentation as needed
• Ensure research activities comply with ethical, regulatory, and data governance standards
• Maintain documentation for study protocols and approvals

Stakeholder Engagement:

• Serve as a key liaison between clinicians, leadership, and external research collaborators
• Support joint research initiatives with partners, payors, and academic institutions
• Present findings internally and externally as needed

About You:

Required:

• Advanced degree (MD, PhD, MPH, MS, or equivalent)
• Experience conducting clinical research or real-world evidence studies
• Strong statistical and data analysis skills
• Demonstrated experience writing and publishing peer-reviewed manuscripts
• Familiarity with cardiovascular clinical research preferred

Preferred:

• Experience with large healthcare datasets (EHR, claims, monitoring data)
• Knowledge of IRB processes and regulatory requirements
• Experience with digital health, virtual care, or outcomes research
• Prior authorship in CV journals or presentations at major cardiology conferences (ACC, AHA, HRS, ESC)

Key Skills:

• Analytical rigor and attention to detail
• Strong scientific writing and communication skills
• Project management and organizational skills
• Ability to work independently and cross-functionally
• Comfortable operating in a fast-paced, evolving environment

Success Metrics:

• Timely delivery of abstracts and manuscripts
• Acceptance of work at major CV conferences and journals
• Clear, reproducible analyses supporting clinical and economic value
• Establishment of a scalable, repeatable research process