88jobs的标志

REGULATORY MEDICAL WRITER PARIS (H/F)

Paris, 法国

> 45k € per year

研发 长期合同 全职

语言水平

英语 - 具有双语能力（口头和书面）

说明

88BIOSCIENCE is a new Lifescience recruitment brand from 88JOBS, the multi-specialist recruitment platform based in Europe and Asia. Our mission is to provide a professional, friendly and overall, reliable service for those looking for work and companies looking for staff.

Today, 88BIOSCIENCE is looking for a REGULATORY MEDICAL WRITER to join a biotech company in Paris. 

The hiring company:
Our client is a pharma company specialized in the research and development of treatments for cancer and neurodegenerative diseases. More than 10 research projects in more than 30 countries are currently being conducted by this company.

The job responsibilities:
  • You will have to handle medical writing of all types of regulatory and clinical study documentation including clinical study reports, clinical summaries, narratives, Investigators’ Brochures and protocols
  • You will have to prepare regulatory responses to health authorities
  • You will manage preparation of marketing authorisation applications (eCTD module 2)
  • You will simultaneously manage several projects and have to meet tight deadlines

The working environment:
  • You will be hired to join the Regulatory Departement team composed of 3 people.
  • You will work in pairs with another Medical Writer.
  • You will directly report to the Senior Regulatory Lead of the company


所需资料

You are the person the hiring company is looking for if:
  • You have a PhD or Masters in Life Science or related fields
  • You are fluent in English. 
  • You have minimum 2 years of experience as a Medical Writer in Industry (biotech, CRO, pharma)
  • You are familiar with working with document templates & style guides

The next steps after submitting your application:
  • A 88BIOSCIENCE consultant will analyse your application and contact you.
  • The consultant will then forward your application to the recruiting company.
  • You will have a first telephone interview with the company's HRD
  • You will have a second face to face interview with the Senior Regulatory Lead of the company.
  • You will have a last round of interview with the Executive Board of the company.
  • You will receive a job offer

A question for us?
  • Send your request to Sophie, sc[@]88jobs.fr



其他信息

Additional information, salary and benefits
  • Start date: as soon as possible
  • Type of contract: Permanent
  • Job type: full time
  • Salary : > 45k € per year
  • Benefits: Transport, partial teleworking possible after the end of trial period

1年前

接受类似工作职位 REGULATORY MEDICAL WRITER PARIS (H/F) 通过电子邮件