Senior Manager/Associate Director, Medical Writing - Corporate Office, San Diego, CA, US

Medical writing manager prepares and reviews clinical/regulatory documents to support drug development. · ...

We are looking for a Medical Writing Manager to lead the authoring process for clinical/regulatory documents. · The Medical Writing Manager will prepare and review high-quality clinical/regulatory documents that comply with internal and external standards. · They will participate ...

We are seeking a Medical Writing Manager to join our team at Neurocrine Biosciences. This role will be responsible for preparing and reviewing clinical/regulatory documents, participating in project teams, and leading the authoring process. · ...

The Associate Director will author high-quality clinical regulatory documents supporting the regulatory requirements of clinical development programs. · ...

The Senior Director Medical Writing will work with cross-functional teams to develop write and review clinical and regulatory documents ensuring the documents are of high quality and comply with internal external standards. · This position reports to the SVP Regulatory Affairs & ...

Job summary · A Medical Writing Intern will support Regulatory and Medical Writing activities at Arrowhead Pharmaceuticals by contributing to preparation of a supplemental New Drug Application (sNDA) and related clinical documentation. This internship offers hands-on exposure to ...

We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, · neuroendocrine and neuropsychiatric disorders.We know what it takes to be great, · and we are as passionate about our people as we are about our purpose - to ...

We are seeking a Sr Manager Medical Writing to lead the writing activities of an interdisciplinary team to develop documents that are concise high quality and comply with internal and external standards. · This role is onsite at our beautiful campus in San Diego CA we offer reloc ...

The Associate Director of Medical Writing will author high-quality clinical regulatory documents supporting regulatory requirements for clinical development programs. · Serves as medical writing lead on clinical regulatory documents. · Collects and interprets data to define probl ...

This is an 11-week Summer Internship Program at Arrowhead Pharmaceuticals. · The Medical Writing Intern will support Regulatory and Medical Writing activities by contributing to preparation of a supplemental New Drug Application (sNDA) and related clinical documentation.Assist wi ...

Mirador is a next-generation precision medicine company focused on immunology and inflammation. The Associate Director, Medical Writing, within the Regulatory Affairs and Quality organization will author high-quality clinical regulatory documents. · ...

· Lead and manage the QC function within Medical Writing, including QC resource allocation, review planning, and oversight of QC timelines across multiple programs and therapeutic areas. · Perform QC activities (editing and data verification) for clinical and regulatory document ...

The Medical Writing Intern will support Regulatory and Medical Writing activities at Arrowhead Pharmaceuticals by contributing to preparation of a supplemental New Drug Application (sNDA) and related clinical documentation. · ...

Arrowhead Pharmaceuticals is seeking an experienced Quality Control (QC) professional to lead the QC function supporting the development of high-quality clinical and regulatory documents across our growing RNAi therapeutic pipeline. · ...

+Job summary · The Manager, Medical Writing Quality will lead the QC function supporting the development of high-quality clinical and regulatory documents across Arrowhead's growing RNAi therapeutic pipeline. · +ResponsibilitiesLead and manage the QC function within Medical Writi ...

Mirador is a next-generation precision medicine company focused on immunology and inflammation. · ...

ClinChoice provides expertise in clinical operations to help partners advance healthcare by accelerating clinical trials. · Coordinate and compile relevant data to complete PSUR reports · Ensure open communication with stakeholders through the PSUR writing process · ...

We are seeking a Sr. Manager for our Medical Writing department to lead the writing activities of an interdisciplinary team. The successful candidate will prepare and review clinical/regulatory documents to support all phases of drug development. · Authors and manages the authori ...

A clinical-stage biopharmaceutical company is seeking an experienced Manager, Medical Writing QC to lead quality control activities for clinical and regulatory documents. · Lead and manage the Medical Writing QC function. · Perform QC review (editing and data verification) for c ...

A clinical-stage biopharmaceutical company advancing an innovative RNAi therapeutic pipeline is seeking an experienced · Manager, Medical Writing Quality Control · to lead quality control activities for clinical and regulatory documents. · ...

The Senior Manager/Associate Director, Medical Writing will author, edit and provide input to documents required for regulatory submissions to US and other global health authorities... · ...