Sr. Manager, Medical Writing - US CA San Diego

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 prepare and review clinical/regulatory documents that are high quality, concise, and comply with internal and external standards in support of all phases of drug development. · ...

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

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. · ...

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 ...

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

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. · ...

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 ...

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. · ...

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 · 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 ...

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 ...

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. · ...

· 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 ...

We are seeking a Senior Manager of Medical Writing to lead our clinical/regulatory document preparation activities. This role will oversee the development of high-quality documents that support all phases of drug development. · ...

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 ...

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

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 ...

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 · ...

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 ...