TG Therapeutics, Inc. is hiring: Medical Writer II/Medical Writer III in Raleigh

Legitimate TG Therapeutics job offers will only come from individuals whose email addresses end in @tgtxinc.com. TG Therapeutics only uses LinkedIn and our TG corporate website for job postings. TG Therapeutics does not use Flock or any other social media platforms other than LinkedIn.

Organizational Overview:
TG Therapeutics is a fully-integrated, commercial-stage, biopharmaceutical company focused on the acquisition, development, and commercialization of novel treatments for B-cell diseases. In addition to a research pipeline including several investigational medicines, TG has received approval from the United States Food and Drug Administration (FDA) for BRIUMVI (ublituximab-xiiy) in the US and European Commission.

Position:
The Medical Writing function plays a critical role in developing high-quality clinical, regulatory, and scientific documents to support global drug development programs. This role is responsible for authoring and leading clear, accurate, and submission-ready documentation aligned with regulatory expectations.

The Medical Writer collaborates closely with cross-functional teams, including Clinical Development, Regulatory Affairs, Biostatistics, and Safety, to ensure documentation is scientifically robust, strategically aligned, and compliant.

This role is intended for experienced medical writing professionals (Medical Writer II or III) with demonstrated ability to independently manage documents and, at the senior level, lead complex deliverables and provide strategic input across studies or programs.

Key Responsibilities:
Document Development & Ownership

Independently author, edit, and manage clinical, regulatory, and scientific documents, including protocols, clinical study reports, investigator brochures, briefing documents, submission components, and related deliverables

Translate complex clinical, scientific, statistical, and regulatory information into clear, concise, and well-structured documents

Ensure accuracy, consistency, and traceability of data across documents, including appropriate source-data verification

Project & Timeline Management

Develop and manage document timelines and deliverables in alignment with study and program milestones

Lead or support document planning, cross-functional review cycles, and comment resolution

Manage multiple concurrent writing projects while proactively identifying risks and dependencies

Cross-Functional Collaboration

Partner with cross-functional teams to align on document strategy, messaging, and data presentation

Integrate input from multiple stakeholders to produce high-quality, submission-ready deliverables

Collaborate with external contributors, including contract writers, vendors, and consultants as needed

Quality & Compliance

Ensure documents comply with regulatory requirements, ICH guidelines, and company standards

Apply strong editorial judgment to improve clarity, structure, and consistency

Maintain version control, documentation, and audit-ready records to support inspection readiness

Process Improvement

Contribute to development and refinement of templates, style guides, and writing processes

Support continuous improvement of medical writing standards and operational efficiency

Leadership & Strategic Contribution (primarily Medical Writer III)

Lead complex or high-priority writing projects and cross-functional initiatives

Provide strategic input on document messaging, organization, and regulatory positioning

Ensure consistency and alignment across multiple documents within a study or submission

Review and provide substantive feedback on work from other writers

Identify risks and proactively recommend solutions related to documentation, timelines, or content gaps

Oversee vendors or contract writers, as applicable

Qualifications:

2-4 years (Medical Writer II) or 5+ years (Medical Writer III) of relevant experience in medical writing, regulatory writing, clinical development, or scientific communications within the biotechnology or pharmaceutical industry

Demonstrated experience authoring clinical and regulatory documents (e.g., clinical study reports, protocols, investigator brochures, submission documents, or manuscripts)

Strong ability to interpret and translate complex clinical, scientific, and statistical data into clear, accurate, and well-structured written content

Working knowledge of drug development processes, clinical research, and regulatory requirements, including familiarity with ICH guidelines

Proven ability to independently manage writing projects, timelines, and cross-functional input

Preferred Qualifications

Experience leading complex or multi-document deliverables or supporting regulatory submissions (e.g., NDAs, BLAs, MAAs)

Ability to provide strategic input on document messaging, organization, and regulatory positioning

Experience ensuring cross-document consistency and submission readiness across studies or programs

Prior experience mentoring junior writers or reviewing the work of others

Experience managing or overseeing external vendors or contract medical writers

Therapeutic area experience in neurology, immunology, autoimmune disease, multiple sclerosis, or related areas

Familiarity with document management systems, collaborative authoring tools, and emerging technologies (e.g., AI-enabled writing tools)

Education:

Bachelor’s degree in life sciences, health sciences, pharmacy, or a related discipline required; advanced degree (e.g., MS, PhD, PharmD) preferred

TG Therapeutics is an equal employment opportunity employer, and does not discriminate on the basis of race, color, religion, gender, sexual orientation, gender identity or expression, age, disability, national origin, ancestry, genetic information, military or veteran status, pregnancy or pregnancy-related condition or any other protected characteristic.

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