Medical Writer Clinical Development

• The Medical Writer is responsible for authoring, reviewing, and coordinating the development of high-quality clinical and regulatory documents that support global clinical development programs.
• This role works closely with cross-functional stakeholders to ensure documents are scientifically accurate, strategically aligned, and delivered according to established timelines and medical writing plans.

• Author, edit, and review clinical and regulatory documents, including:
• Clinical study protocols and protocol amendments
• Investigator Brochures (IBs)
• Clinical Study Reports (CSRs)
• Briefing Book support
• IND and NDA summary documents and other regulatory submission materials
• Develop documents that are consistent with regulatory requirements, internal standards, and medical writing plans, while supporting the overall clinical development lifecycle and program objectives for one or more clinical development programs.
• Collaborate with cross-functional teams, including Clinical Development, Clinical Operations, Biostatistics, Data Management, Regulatory Affairs, Pharmacovigilance, and Medical Affairs, to gather, interpret, and integrate scientific and clinical information into clear, accurate, and submission-ready documents.
• Negotiate document deliverable milestones and timelines with cross-functional teams to ensure alignment across functions and adherence to medical writing plans and program objectives.
• Facilitate document review cycles, resolve reviewer comments, and drive consensus among stakeholders while maintaining quality and schedule commitments.
• Ensure documentation complies with applicable regulatory guidance, Good Clinical Practice (GCP), company standards, and industry best practices.
• Contribute to the development and continuous improvement of medical writing processes, templates, style guides, and operational procedures.
• Support regulatory submissions, health authority interactions, and inspection readiness activities as needed.

• Scientific and regulatory writing expertise
• Project and timeline management
• Cross-functional collaboration and influence
• Strategic thinking and problem solving
• Attention to quality and regulatory compliance
• Effective communication and stakeholder management

• Advanced degree Bachelor's degree or more.
• Experience authoring clinical and regulatory documents within the pharmaceutical, biotechnology, or clinical research industry.
• Strong knowledge of clinical development, regulatory requirements, and applicable guidance documents (e.g., ICH guidelines).
• Excellent scientific writing, editing, and communication skills.
• Demonstrated ability to manage multiple projects and negotiate timelines in a cross-functional environment.
• Strong organizational skills, attention to detail, and ability to work independently and collaboratively.

• Advanced degree Bachelor's degree or more

Why TalentBurst?
At TalentBurst, we deliver more than talent, we deliver outcomes. We partner with you to move quickly and connect you to opportunities aligned with your skills and long term growth.

Backed by precision, transparency, and results, we connect top talent with leading organizations through trusted partnerships.

We offer competitive compensation and comprehensive benefits, including medical, dental, vision, and retirement options.

TalentBurst is an equal opportunity employer committed to an inclusive and diverse workforce.

Founded in 2002 by three former Monster.com executives; TalentBurst is an award-winning full-service Staffing Firm working directly with Fortune 500 companies in the US and Canada. We specialize in Contract and Contract to Permanent roles across many industries and have direct/contractual relationships with all our clients. Please visit our website www.talentburst.com or come meet us at our offices in Natick, MA, Miami, FL, Christiansburg, VA, Vineland, NJ, Houston, TX & downtown San Francisco, CA