What are the responsibilities and job description for the Agios Pharmaceuticals is hiring: Associate Director, Medical Writing in Cambridg position at Agios Pharmaceuticals?
Associate Director, Medical Writing
Who we are :
Agios is a biopharmaceutical company that is fueled by connections. We thrive in a supportive, fun, and flexible environment full of people empowered to bring their whole selves to work. We care deeply about our work, each other, and the patients who count on us. Our teams cultivate strong bonds with patient communities, healthcare professionals, partners, and colleagues, which helps us discover, develop and deliver therapies for genetically defined diseases – and make a bigger difference in their lives. In the U.S., Agios markets a first-in-class pyruvate kinase (PK) activator for the treatment of hemolytic anemia in adults with PK deficiency. Building on the company’s leadership in the field of cellular metabolism, Agios is advancing a robust clinical pipeline of investigational medicines with active and planned programs in alpha- and beta-thalassemia, sickle cell disease, pediatric PK deficiency and MDS-associated anemia.
The impact you will make :
Agios Pharmaceuticals is searching for a dynamic Associate Director, Medical Writing to join our growing Regulatory Affairs & Medical Writing team. We want someone who cares about this important work, and who’s driven to connect to our mission of helping these patient communities. This position reports directly to the Director, Head of Medical Writing. The Associate Director, Medical Writing oversees the development of high-quality clinical regulatory documents, including but not limited to, protocols, IBs, CSRs, and clinical sections of submissions. The Associate Director, Medical Writing is also responsible for leading and mentoring team members while successfully implementing the vision for the department.
What you will do :
- Work with and lead project teams to prepare clinical regulatory documents, including but not limited to, protocols, IBs, CSRs, and clinical sections of submissions.
- Coordinate the efforts of cross-functional teams to produce high-quality, scientifically accurate documents; contribute to overall project management to facilitate efficient document development and finalization.
- Author documents; Manage the writing and completion of documents and other assigned tasks within established timelines and with highest quality in terms of scientific content, organization, clarity, accuracy, format, consistency, and adherence to regulatory and internal guidelines, styles, and processes through both internal and external writing resources.
- Ensure that deliverables meet all applicable regulations, standards, and guidelines, including International Conference on Harmonisation (ICH) guidelines and EU Clinical Trial Regulation.
- Assists Head of MW in designing and maintaining templates and standards for clinical documents in accordance with ICH guidelines and medical writing best practices.
- Represent the Medical Writing function on clinical study teams.
- Oversee CRO vendors and consultants.
What you bring :
What we will give you :
Interested in learning more about what makes our culture unique? Visit the Inside Agios section of our website.
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