Sr. Medical Writer

* Research, write, edit, and annotate scientific and medical materials, including:
* Manuscripts, abstracts, posters, and congress materials
* Slide presentations and advisory board content
* eLearning modules, digital assets, and medical/commercial communications
* Patient- and lay-audience materials
* Conduct literature reviews, data analysis, and MLR review support.
* Ensure scientific accuracy, consistency, and compliance with AMA, journal, congress, client, and regulatory requirements.
* Contribute to scientific narratives, communication platforms, and strategic content development.
* Manage document version control and maintain high-quality deliverables.

Client Engagement & Strategic Support

* Act as a scientific lead during client meetings, workshops, and advisory boards.
* Provide scientific expertise and strategic recommendations aligned with client objectives.
* Support business development efforts through scientific insights and proposal content.

Scientific Communications & Publication Planning

* Participate in publication and communication planning activities.
* Identify potential authors, target journals, and congress opportunities.
* Support execution of publication strategies and timelines.

Leadership & Collaboration

* Mentor junior writers and provide editorial review and guidance.
* Collaborate with cross-functional teams to ensure scientific accuracy and consistency across projects.

Core Competencies

* Strong organizational, project management, and decision-making skills.
* Ability to manage multiple priorities and deadlines in a fast-paced environment.
* Professionalism under pressure and a collaborative approach to teamwork.
* Strong client relationship management and problem-solving capabilities.

Education

* Advanced scientific or healthcare degree preferred (PhD, PharmD, MD, MSc, or equivalent).
* Relevant bachelor's or master's degree with substantial experience may be considered.

Experience

* Approximately 2+ years of medical writing experience in a medical communications agency, pharmaceutical, or related environment.
* Experience interacting with clinicians, KOLs, medical experts, and cross-functional stakeholders.
* Ability to work independently with minimal supervision.

Skills

* Exceptional scientific writing, editing, analytical, and communication skills.
* Strong understanding of clinical research, drug development, data interpretation, and regulatory requirements.
* Proficiency in Microsoft Office, Adobe Acrobat, graphing/figure-generation tools, and virtual collaboration platforms.
* Strong leadership, mentoring, and interpersonal skills.

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