Medical Writer Jobs in Durham, NC

Engage as a senior medical writer driving clarity in clinical and regulatory documents. Collaborate across teams, lead projects, and provide mentorship while adhering to regulatory standards and deliv...

Develop clear, accurate medical documents for clinical studies, leading technical teams and collaborating with clients. Ensure adherence to regulatory standards while mentoring junior writers and mana...

Grow your career with a leading role in medical writing, managing clinical documentation and regulatory projects. Contribute your expertise in writing and editing while collaborating with cross-functi...

Lead the charge in delivering high-quality medical writing for clinical and regulatory projects, ensuring compliance with industry standards while collaborating closely with internal teams and clients...

Partner with us to deliver high-quality clinical documents for regulatory submissions, ensuring compliance and excellence in project execution while mentoring team members in a collaborative environme...

Champion the preparation and quality assurance of clinical documents, ensuring compliance and accuracy for regulatory submissions while supporting team development and executing project activities wit...

Join a team that's dedicated to Clinical Trial Transparency, executing high-quality project activities within defined timelines. Contribute to regulatory documentation and quality assurance in a colla...

Unlock potential by leading the development of high-quality scientific publications, mentoring junior writers, and shaping clear narratives from complex data in a collaborative medical communications...

Optimize clinical document creation for global regulatory submissions. Lead medical writing projects, ensuring high-quality, data-driven deliverables while mentoring junior staff and collaborating acr...

Lead the charge in crafting high-quality regulatory clinical documents while mentoring junior writers. Drive strategic direction across cross-functional teams to ensure timely, data-driven submissions...

Lead the charge in high-quality medical writing, overseeing clinical and regulatory documents while collaborating with cross-functional teams to ensure precision and clarity. Mentor junior writers and...

Elevate regulatory documentation processes by leading the development and management of comprehensive submission documents, ensuring compliance with global standards while maintaining timelines and co...

Champion the development of regulatory documents for global submissions, overseeing cross-functional collaborations and maintaining adherence to project timelines while ensuring compliance with ICH gu...

Join a dynamic team to create impactful scientific communications that enhance patient outcomes and drive client success through strategic storytelling in a fast-paced, collaborative environment...

Join a team that's shaping the future of medical writing by leading the development of clinical documents for global regulatory submissions. Utilize your strategic expertise to mentor writers and ensu...

Lead the creation and management of regulatory and clinical documents, ensuring compliance and scientific rigor. Collaborate with cross-functional teams to enhance writing standards and practices, sup...

Shape the future of healthcare by leading high-quality medical writing projects. Collaborate with cross-functional teams to produce regulatory documents, ensuring scientific accuracy and compliance to...

Elevate the quality of regulatory documents by providing expert editing, quality control, and mentorship. Drive project success by ensuring compliance with FDA and EU guidelines while leading editoria...

Lead the charge in optimizing medical writing operations while ensuring regulatory documents meet the highest quality and compliance standards. Collaborate cross-functionally to enhance document proce...

Take ownership of regulatory document development for global submissions, ensuring adherence to ICH guidelines and corporate objectives while managing timelines and collaborating with cross-functional...

Unlock potential by leading the development of critical regulatory documents for global submissions while managing timelines and collaborating with cross-functional teams in the oncology space to ensu...

Elevate your career by ensuring compliance and quality in regulatory writing. Lead editorial efforts, provide mentorship, and manage complex projects while interacting with cross-departmental teams to...

Lead the editorial team in ensuring compliance and quality of medical documents. Manage complex projects, perform quality reviews, and mentor staff while adhering to regulatory standards. Drive proces...

Help us ensure compliance and quality in regulatory documents through expert editing and review. Lead projects, mentor staff, and maintain high standards for clinical materials. Bring your editorial e...

Enhance document quality and compliance through expert editing and review. Lead complex medical writing projects, mentor teams, and ensure adherence to regulatory standards while managing timelines an...