Senior Director, Medical Writing - Redwood City
3 days ago

Job summary
We are seeking a Senior Director of Medical Writing to join our team. This is a full-time position that will be responsible for helping to develop strategic leadership and management of the medical writing function.
Job description
, consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare.
Donec lacinia nisi nec odio ultricies imperdiet.
Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula.
Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit
, at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus.
Access all high-level positions and get the job of your dreams.
Similar jobs
Corcept is a leading company in cortisol modulators research and development. The Associate Director of Medical Writing will provide strategic expertise to prepare high-quality clinical regulatory documents for Health Authority submissions. · ...
1 month ago
We are leading the way in the research and development of cortisol modulators. · We have discovered more than 1,000 selective proprietary cortisol modulators. · Develop and execute strategies for organizing and preparing documents for regulatory health authority submissions · Pla ...
6 days ago
We are seeking a Senior Director of Medical Writing to join our team. As a new member of Revolution Medicines, you will be responsible for helping to develop strategic leadership and management of the medical writing function. · Driving for success in terms of people, projects, a ...
2 days ago
Piper Companies is currently seeking an Executive Director of Medical Writing in Palo Alto, California. · ...
2 weeks ago
Job Description: · Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate and transform lives of patients worldwide. · The Associate Director, Medical Writing role involves authoring regulatory documents for clinical programs within one or more program te ...
5 hours ago
The Associate Director Medical Writing is responsible for preparing high-quality medical writing deliverables within one or more program The incumbent will ensure strategically aligned communication points are conveyed in medical writing deliverables and that communication points ...
1 week ago
The Associate Director Medical Writing is responsible for preparing high-quality medical writing deliverables within one or more program. · Works with cross functional teams to author regulatory documents (eg, protocols, clinical study reports) · ...
1 week ago
The individual in this role will serve as an expert Medical Writer who is responsible for planning, developing, and writing clinical documents to support medical and regulatory activities across the portfolio by ensuring that scientifically robust messages and arguments are devel ...
6 days ago
Jazz Pharmaceuticals es una empresa biotecnológica global cuya finalidad es innovar para transformar las vidas de los pacientes y sus familias. · ...
2 days ago
We are seeking an Executive Director of Medical Writing in Palo Alto, California. The Executive Director will oversee the Cardiology medical writing activities across clinical development programs, · Please see below for more details:Oversee the Cardiology l Medical Writing group ...
2 weeks ago
The Associate Director Medical Writing is responsible for preparing high-quality medical writing deliverables within one or more programs. · Works with cross functional teams to ensure effective communication of data in documents. · Analyzes study level documents for their abilit ...
2 days ago
+Job summary · The Director , Medical Writing (MW) responsible managing MW quality review activities in conjunction Head of MW timely accurate efficient manner in compliance company global regulations. · +ResponsibilitiesEnsure appropriate communication project program-related ma ...
5 days ago
We are excited to expand our multidisciplinary team of individuals focused on creating revolutionary medicines to address the unmet needs of patients. · Lead the medical writing function. · Author and review clinical and regulatory documents. · Collaborate with cross-functional p ...
6 days ago
The Associate Director is responsible for writing scientific publications connected with Ascendis' clinical trials in endocrine indications. The role involves cross-functional collaboration and requires a strong understanding of scientific content and translation skills. · Key re ...
1 week ago
Septerna is seeking an experienced Director of Medical Writing to lead the development and execution of medical writing activities across our clinical programs. · Responsibilities Lead the medical writing function and establish best practices, processes, and standards to support ...
1 week ago
We are seeking an Associate Director to join our Global Medical Writing team. The successful candidate will be responsible for writing scientific publications connected with Ascendis' clinical trials in endocrine indications. · ...
1 week ago
We are seeking a Medical Writing Specialist to help design AI systems that write regulatory documents and bridge the gap between domain expertise (medical writing) and technical product development. · Evaluating AI-generated content quality and identifying edge cases. · Bridging ...
4 weeks ago
This position will report to the Medical Writing Department Head and lead scientific medical and regulatory writing activities for development projects ensuring full life-cycle support from clinical study protocols through regulatory submission and post-approval activities that d ...
1 month ago
This position will report to the Medical Writing Department Head and will lead scientific medical regulatory writing activities for development projects ensuring full life cycle support from clinical study protocols through regulatory submission and post approval activities that ...
1 month ago
This position will report to the Medical Writing Department Head and will lead scientific, medical and regulatory writing activities for development projects. · ...
1 month ago