Clinical Research Writer

This is a fully remote position, open to applicants in United States.

📋 Description

• Develop and uphold a structured research roadmap that aligns with the clinical priorities of the organization.

• Organize research initiatives across various clinical programs and engage multiple stakeholders.

• Create standardized procedures for study design, data requests, analysis, and publication timelines.

• Facilitate collaboration among clinical, data, product, and operations teams.

• Analyze extensive clinical and administrative datasets, including EHR, monitoring data, and claims when available.

• Perform outcomes, quality, and utilization analyses utilizing appropriate statistical methods.

• Collaborate with data teams to outline data requirements and ensure data quality and integrity.

• Convert analyses into clinically relevant insights and conclusions.

• Lead the authorship and coordination of abstracts, posters, and manuscripts for cardiovascular conferences and journals.

• Draft and refine manuscripts in partnership with clinical leaders and co-authors.

• Oversee submissions to conferences and peer-reviewed journals.

• Assist in addressing reviewer comments and making necessary revisions.

• Support IRB submissions, exemptions, and the preparation of regulatory documentation.

• Ensure adherence to ethical, regulatory, and data governance standards.

• Maintain comprehensive documentation for study protocols and approvals.

• Act as a liaison between clinicians, leadership, and external research collaborators.

• Support collaborative research initiatives with partners, payors, and academic institutions.

• Present findings to internal and external stakeholders as required.

⛳️ Requirements

• An advanced degree (MD, PhD, MPH, MS, or equivalent) is required.

• Proven experience in conducting clinical research or real-world evidence studies.

• Strong skills in statistical analysis and data interpretation.

• Demonstrated experience in writing and publishing peer-reviewed manuscripts.

• Familiarity with cardiovascular clinical research is preferred.

• Experience with large healthcare datasets (EHR, claims, monitoring data) is preferred.

• Knowledge of IRB processes and regulatory requirements is preferred.

• Experience in digital health, virtual care, or outcomes research is preferred.

• Prior authorship in cardiovascular journals or presentations at major cardiology conferences (ACC, AHA, HRS, ESC) is preferred.

• Strong analytical rigor and attention to detail.

• Excellent scientific writing and communication skills.

• Effective project management and organizational skills.

• Capability to work independently and collaboratively across functions.

• Comfortable working in a fast-paced and evolving environment.

🏝️ Benefits

• Full-time employment.

• Remote-first work environment offering flexibility, autonomy, and trust.

• Equal opportunity employment.

• Mission-driven work aimed at revolutionizing cardiovascular care.