Medical Writing Manager - San Diego, CA

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. · ...

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 ...

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

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 ...

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. · ...

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. · ...

· 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 ...

+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 ...

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 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. · ...

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

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... · ...

We are seeking a Senior Manager/Associate Director of Medical Writing to join our team at Avenzo Therapeutics. The successful candidate will be responsible for authoring and editing regulatory documents, presentations, posters, publications and fulfilling regulatory requirements. ...

A client is looking to hire UX Writer / Content Designer who can come on site in San Diego. · ...

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 & ...

++The purpose of the study director position is to provide hands-on experimental study design validation execution analysis and reporting of oncology related studies at Crown Bioscience San Diego. · +,++Study design protocol development and optimization and study report writing a ...

The Applications team is looking for a technical writer to work on software specifications and user interface copy for Apple Creator Studio. · ...

We are seeking a talented Senior Content Designer to join our client's dynamic storytelling team. · This role offers the unique opportunity to shape how innovative financial technology solutions are presented to both internal stakeholders and external audiences. · You'll work at ...