Medical Writer Jobs in Durham, NC

Lead the charge in producing high-quality medical documents while collaborating with cross-functional teams to ensure regulatory compliance and clear scientific communication. Mentor junior writers an...

Unlock your potential by leading medical writing initiatives, ensuring clarity and compliance in scientific documentation while mentoring peers. Collaborate cross-functionally to deliver high-quality...

Join a dynamic team as you lead impactful medical writing projects, ensuring clarity and accuracy in clinical documentation while mentoring junior writers and collaborating across departments to meet...

Champion the creation of accurate medical writing deliverables, coordinating cross-departmental activities with minimal supervision. Ensure adherence to regulatory standards while mentoring junior wri...

Drive the precise execution of medical writing projects, ensuring compliance with regulatory standards while collaborating across departments. Leverage expertise to mentor junior writers and deliver h...

Create impactful medical publications by collaborating with cross-functional teams. Contribute your expertise to elevate scientific communications while advancing your career in a dynamic, rewarding e...

Take ownership of high-quality project execution, ensuring timely delivery of clinical documents and regulatory submissions while collaborating across teams to support clinical trial transparency effo...

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...

Accelerate progress at the intersection of clinical transparency and quality. Engage in high-impact writing and quality assurance for regulatory documents, collaborating with diverse teams to ensure c...

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...

Champion the development of clinical documents for global regulatory submissions, ensuring accuracy and compliance while leading cross-functional teams and mentoring junior writers to deliver high-qua...

Shape the future of global regulatory submissions as a senior leader driving high-quality clinical documentation. Collaborate with cross-functional teams to ensure compliance and precision, while ment...

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...

Lead the charge in developing regulatory documents for global submissions, ensuring compliance with ICH guidelines while managing projects across teams to support timely delivery and corporate objecti...

Engineer impactful clinical documents while leading cross-functional teams. Contribute to regulatory submissions with strategic oversight, ensuring clear data presentation and compliance. Mentor junio...

Advance your career by crafting high-quality clinical study documents. Lead the development process while ensuring compliance with regulatory guidelines. Collaborate effectively within teams to delive...

Grow your career with a dynamic role crafting essential clinical and regulatory documents. Drive document strategy, mentor teams, and enhance processes to ensure timely, quality submissions in a fast...

Engage with a dynamic team to lead and craft high-quality clinical documents while ensuring compliance with regulatory standards and precision in messaging throughout all phases of development...

Transform the future of healthcare by developing critical clinical and regulatory documents that ensure product compliance and approval. Lead document management, mentor team members, and contribute t...

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...

Explore an impactful role driving quality and compliance in regulatory documents, leading editorial projects, and mentoring medical editing staff to ensure adherence to industry standards and enhance...

Advance your career by managing complex regulatory writing projects, ensuring compliance and collaboration across global teams. Engage in impactful medical writing for oncology submissions, shaping th...