Remote Medical Writer — Regulatory & Clinical Reporting

MSD

United States

À distance

USD 96 000 - 151 000

Plein temps

14 jours+

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Avantages offerts par ce poste

Medical, dental, vision benefits
401(k) and retirement benefits
Paid holidays and vacation days

Résumé du poste

MSD is seeking a data-minded professional to support clinical research coordination, trial design review, and regulatory documentation. You will collaborate with cross-functional teams to ensure timely data analysis, reporting, and compliant documentation.

Proficiency in MS Office and SharePoint is required, with a willingness to learn emerging technologies. This remote-friendly role offers a comprehensive benefits package and opportunities to contribute to regulatory submissions.

Qualifications

  • Bachelor's degree in a health, scientific, or related discipline with 2+ years industry experience.
  • Knowledge of clinical research principles, trial design, and statistics.
  • Attention to detail with strong analytical and data interpretation skills.
  • Ability to manage multiple projects in a deadline-driven environment, independently and in teams.
  • Strong written and verbal communication for stakeholder interactions.
  • Proficiency in Microsoft Office and SharePoint; openness to learn new tech.

Responsabilités

  • Coordinate activities across multiple clinical study projects.
  • Critically evaluate data and interpret results for accuracy.
  • Prepare and manage regulatory documents and study materials.
  • Communicate findings and project updates to stakeholders effectively.

Connaissances

Clinical research
Analytical thinking
Project management
Communication skills
Cross-functional collaboration
Microsoft Office
SharePoint

Formation

Bachelor's degree

Outils

Microsoft Office Suite
SharePoint

Description du poste

MSD is seeking a data-minded professional to support clinical research coordination, trial design review, and regulatory documentation. You will collaborate with cross-functional teams to ensure timely data analysis, reporting, and compliant documentation.

Proficiency in MS Office and SharePoint is required, with a willingness to learn emerging technologies. This remote-friendly role offers a comprehensive benefits package and opportunities to contribute to regulatory submissions.

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