R&D - CSO - Sr. Medical Writer I - BJ - Beijing

This environment encourages innovation, individuality and embraces people that want to be a part of it. · ...

Join Us as a Principal Medical Writing - Make an Impact at the Forefront of Innovation As a Principal Medical Writer you will serve as the primary author by writing and providing input on routine documents such as clinical study reports and study protocols summarizes data from cl ...

This role involves writing routine documents such as clinical study reports and study protocols summarizing data from clinical studies. · Provide high-quality medical and scientific writing from planning to delivery of final drafts to clients. · ...

This role will serve as the primary author by writing and providing input on routine documents such as clinical study reports and study protocols. · Provide high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and ...

Join Us as a Principal Medical Writing - Make an impact at the forefront of innovation. · Provide high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients. · ...

Join Us as a Principal Medical Writing - Make an Impact at the Forefront of Innovation As a Principal Medical Writer you will serve as the primary author by writing and providing input on routine documents such as clinical study reports and study protocols summarizes data from cl ...

We are seeking a Principal Medical Writer to join our team. As the primary author, you will write and provide input on routine documents such as clinical study reports and study protocols. · As the lead writer review documents for the team and provide training and guidance to jun ...

We are seeking a Principal Medical Writer to join our team as a primary author of routine documents such as clinical study reports and study protocols. · Provide high-quality medical and scientific writing from planning and coordination through delivery of final drafts to interna ...

Lead writer independently responsible for the preparation of clinical study protocols and clinical study reports (CSRs), and other documents as needed for lower complexity studies. · ...

We are seeking a skilled Associate Medical Writer to join our team. The successful candidate will provide complex study reporting and project services to department personnel. · Provide study reporting and project services to the team. · Compile, organize and publish clinical stu ...

This job is with Thermo Fisher Scientific. Join Us as a Compilation Specialist - Make an impact at the forefront of innovation. · Provide study reporting and project services to the team. · ...

The Compilation Specialist provides complex study reporting and other project services to department personnel. · Compiles, coordinates, revises and finalizes appendix documents.The role involves interaction with project teams within the company and in many cases direct contact w ...

Join us as a compilation specialist and make an impact at the forefront of innovation. The role involves complex study reporting and project services to department personnel. · ...

Create high-quality clinical documents for regulatory submissions Ensure timely delivery while maintaining compliance with standards and high quality Lead implementation of new digital technologies and AI solutions ...

Create high-quality clinical documents for regulatory submissions Ensure timely delivery while maintaining compliance with standards and high quality Lead implementation of new digital technologies and AI solutions Drive process improvements for efficiency gains Mentor junior wri ...

As a Senior Medical Writer I at Sanofi in Beijing, China, you will create high-quality clinical documents for regulatory submissions while ensuring timely delivery and compliance with standards. You will lead the implementation of new digital technologies and AI solutions to driv ...

We are seeking a Research Consultant to join our team. · The successful candidate will be responsible for deducing clinical trends, monitoring secondary information from various sources, and conducting market research with senior support. · Deduce clinical trends, differentiation ...

The Associate Director Medical Writing oversees the regional Medical Writing staff and projects, ensuring the delivery of quality products within agreed timelines. · This role involves assisting in the development of the Medical Writing organizational structure, as well as recrui ...

The Associate Director Medical Writing oversees the regional Medical · Writing staff and projects ensuring delivery of quality products within agreed timelines. · Manage the operation of a Medical Writing group to include management of workload departmental resources allocation o ...

The Sr. Clinical Evidence Planning & Evaluations Manager for GCN under Clinical Affairs team- Global Medical Affairs is responsible for providing expert clinical evidence planning evaluation and medical writing in support of product registration post-market surveillance PMS promo ...