Senior Medical Writing Leader – Global Regulatory Submissions

Job Description Overview Job Summary (Primary function) The Associate Director, Principal Medical Writer II is responsible for the development of clinical documents for submissions to regulatory authorities globally. Provides strategic direction to cross‑functional project teams with minimal oversight to ensure that clinical documents (eg, Investigators'...

4943 - Morges, Switzerland - Switzerland - Research **Overview** Job Summary The Associate Director, Principal Medical Writer I is responsible for the development of clinical documents for submissions to regulatory authorities globally. Provides strategic direction to cross-functional project teams with mínimal oversight to ensure that clinical documents...

Overview: **Background** This role is based in the Global Headquarters in Morges, Switzerland reporting to the Senior Manager Global Launch Projects, Partner Markets located in Switzerland. ** Job Summary (Primary function)** This position plays a key role in operationalizing the alliances and partnerships projects for pre-commercial and launch...

**Job Summary** This position is responsible for quality control (QC) review of clinical documents intended for submission to health authorities worldwide. The Clinical Editor will copyedit/proofread, format, and verify data content in clinical documents in accordance with company SOPs and processes to ensure documents meet required standards. This position...

A global biopharmaceutical company in Morges, Switzerland is seeking a Project Manager to oversee alliances and partnership projects. The role requires advanced project management skills, strong communication abilities, and a proven record in managing global projects effectively. Ideal candidates will hold a Bachelor's degree in Business or related fields,...

Some highlights Being part of an international company yet with local presence Build a safer digital society together with us Working as a Security Incident & Vulnerability Management Lead The Security Incident & Vulnerability Management Lead’s mission and objective will be to establish, maintain and orchestrate the Security Incident & Vulnerability...

OverviewSummaryThe Sr. Director Clinical Research Scientist is responsible for working with the physicians within Clinical to provide clinical research support for programs as assigned by phase or therapeutic area.Duties and ResponsibilitiesAct within compliance and legal requirements as well as within company guidelines.Contribute positively to a strong...

**Give hope. Give health. Make your mark in the fight against cancer.** At Accuray, we make a direct and powerful impact on the lives of cancer patients every day — helping them live longer, better lives. But our commitment to innovation offers a truly unique opportunity: the chance to change the fight against cancer — helping to develop, introduce and...

**Some highlights**: - Being part of an international company yet with local presence - Build a safer digital society together with us Orange Cyberdefense is the expert cyber security business unit of the Orange Group, providing security consulting, solutions and services to organisations around the globe. We strive to protect freedom and build a safer...

**Summary** The main objective of this position is to develop appropriate health economic and outcomes research evidence to characterize INCYTE products value at launch and throughout their life cycle. **Responsibilities** - Initial focus will be on the upcoming launches including pemigatinib and tafasitamab but also earlier products in the pipeline. -...