As a Sr. Medical Writer, you will join the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.
What you will be doing:
- Independently author study-level documents at various complexity levels, including:
- Protocol and protocol outlines
- Subject Information and Informed Consent forms
- Clinical Study Reports (CSRs)
- Lay summaries of clinical trial results
- Investigator Brochures (IBs)
Support experienced writers in preparing submissions and complex clinical documents.Interpret and summarize data effectively.Lead discussions, ensure decision-making, and incorporate project strategies into documents.Lead meetings and make decisions on project-specific medical writing issues.Manage all aspects of medical writing tasks, including stakeholder alignment, coordination, and meeting deadlines.Perform other duties as assigned.Qualifications and Skills:
- Proactive team player with strong stakeholder relationship skills.
- Excellent facilitation, communication, and problem-solving skills.
- Ability to work independently, resourceful in following SOPs and guidelines.
- Strong project management and organizational skills.
- Ownership of tasks and drive to finalize documents.
What you need to possess:
- Proactive team spirit.
- Ability to establish and maintain good working relationships.
- Engagement with stakeholders to understand and align on project goals.
- Effective communication and decision-making skills.
- Ability to work independently and demonstrate resourcefulness.
- Strong time management and organization skills.