The Perfect Addition to Our Team. You have a resourceful, collaborative, and versatile approach to work and bring extensive medical writing expertise. You are comfortable interacting with cross functional stakeholders and have a keen eye for detail. You are someone who thrives in a start-up environment, and have the ability to identify potential solutions to current and future challenges. The Opportunity. The Associate Director, Regulatory Writin...
The Role. Nuvalent is seeking a highly-motivated, results-oriented team member to join our growing organization as Associate Director, Medical Writing. This role, which will report to the VP, Clinical Development, will partner with departmental leadership to strengthen Nuvalent’s medical writing capabilities and quality standards as well as leading various medical writing projects across Nuvalent’s growing clinical pipeline. Responsibilities. Pro...
Job Summary. The Medical Writer will lead medical writing activities for clinical documentation preparation to support the advancement of clinical-stage programs. Primary Responsibilities. Coordinate the preparation and timely delivery of high-quality documents for domestic and international regulatory filing and clinical programs. Produce documents to support clinical trials and regulatory submissions, in accordance with domestic and internation...
Associate Director, Medical Writing. Location. Lexington, 113 Hartwell Ave. Education level. Bachelor / Graduate. Job category. Clinical Operations. Target start date. 5/29/2023. Work Location. Flex. Shift. 1st. . uniQure is dedicated to bringing innovative therapies or unmet medical needs to patients. In doing so each function in uniQure is directly or indirectly responsible for the lives of patients. This responsibility should be part of our da...
